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Bibhas Pandit et al. Int. Res. J. Pharm. 2021, 12 (12) INTERNATIONAL RESEARCH JOURNAL OF PHARMACY www.irjponline.com ISSN 2230 – 8407 Review Article A REVIEW ON THE RESTORATIVE IMPACT OF ACACIA ARABICA Bibhas Pandit 1*, Ritika Singh 2, Honey Jajo 1, Trilochan Satapathy 3 1 Department of Pharmaceutical Chemistry, Himalayan Pharmacy Institute, Majhitar, Rangpo, Sikkim, India 2 Department of Pharmacology, Rungta College of Pharmaceutical Sciences and Research, Raipur, Chhattisgarh, India 3 Department of Pharmacy, Pt Deendayal Upadhyay Memorial Health Sciences and Ayush University, Raipur, Chhattisgarh, India *Corresponding Author Email: bibhas.pandit@gmail.com Article Received on: 03/12/21 Approved for publication: 17/01/22 DOI: 10.7897/2230-8407.1212173 ABSTRACT From ancients, herbal medicines are used in the management and cure of various physiological abnormalities. In this 21st century, a huge part of the world's population still depends mostly on the conventional system of medicine as these medicines are economical, easily available, and have minimal side effects. Acacia arabica commonly known as Babool, indigenously found in India possessed a variety of pharmacological effects when used in different traditional formulations. There are about 1350 Acacia species available worldwide. In India, Acacia arabica is widely spread in Jammu, Himachal Pradesh, Uttar Pradesh, Punjab, Madhya Pradesh, Orissa Bihar, and Andhra Pradesh. The use of Acacia arabica in the traditional formulation is popularized due to its diverse pharmacological activity. Recent research on Acacia arabica revealed that the plant is rich in antioxidants such as catechin, ellagic acid, epigallocatechin, kaempferol, gallic acid and is used in the treatment of inflammation, pain, diabetes, allergy, asthma, bronchitis, amoebiasis, dermatitis, and cardiovascular diseases like hypertension, atherosclerosis, and myocardial infarction. Acacia arabica is also found to be efficient in infection caused by bacterial, fungus, and protozoa. In this present review, our sincere efforts have been given to summarize the various biological active ingredients of Acacia arabica and their pharmacological effects reported by different researchers. Keywords: Acacia arabica; herbal medicine; antioxidants; babool; traditional formulations. INTRODUCTION Herbal-based medicines date backside numerous centuries to the Rig-Veda, the set of Hindu revered verses is the source of a physical condition system known as Ayurvedic medicine1. The individual helpful plant that has moved toward from Ayurvedic tradition is Acacia arabica2. The antique report points out that, all parts of the global citizen revealed and developed medicinal uses of neighboring plants. When skill progressed, a dichotomy in medication developed between practitioners of herbal medicine and usual physician3. The majority of the herbal-based remedies had a resonance scientific basis and a few became functional prescriptions drugs. Now a day’s medicinal plants still supply appreciably to prescription drugs and 35% of prescriptions printed in the U.S. include plant-derived vigorous ingredients4. Significance in medicinal plants has to pay attention to native people in various parts of the world. There are about 1350 Acacia species available worldwide5. In India, one of the acacia species, commonly known as Acacia Catechu is widely spread in Jammu, Himachal Pradesh, Uttar Pradesh, Punjab, Madhya Pradesh, Orissa Bihar, and Andhra Pradesh6. Different parts of the Acacia plant such as bark, flowers, leaves, seeds, roots, and pods are used by traditional healers for the treatment of many ailments by many cultures7-8. It has an extensive division in Africa and Asia, it is insidious and capable to adjust the unreliable environmental situation and major parts of the plant have been used to care for diverse ailments. Further often studied on acacia in the ancient world include Acacia confusa, Acacia nilotica, and Acacia catechu. Amongst African acacias, Acacia aroma is a mainly investigated species due to its cost-effective significance as a foundation of strong tannins9-10. This chapter offers a recent and complete review of acacia species, covering their taxonomical, ethnomedicinal, chemical, and pharmacological features. Taxonomy The acacia is a large genus of 1350 species, the second largest among the Fabaceae11. The name Acacia originated from an African species. This name comes from the Greek word “akakia” which means “thorn” as varieties of the African Acacia species contain thorn. Acacia is one of the largest genera with two subgenera, Acacia aculeiferum and Acacia phyllodineae. Both subgenera were crops at the genus level, but the reclassification of this plant has not been largely determined due to insufficient supporting data. Recently, molecular evidence suggested five genera of Acacia12. African haunted species original kind of Acacia Acacia Thus, if Acacia was dividing into five genera along with the original African type, then whole 960 Australian species have required to converted innovative name. Therefore, Orchard and Maslin anticipated that the forms of Acacia be converted from American species (Acacia catechu) to an African species (Acacia penninervis)13. And remaining 500 species (mainly in America and Africa) would require a name alter. In 2004, this contentious offer concerning the name of Acacia was official at the 107 International Botanical Congress14. On the other hand, as the immense greater part of the journalism, first and foremost relating 7 Bibhas Pandit et al. Int. Res. J. Pharm. 2021, 12 (12) to phytochemistry, treats Acacia as of the major genus, i.e. this move toward is also used in this manuscript. ACACIA AS ETHNOMEDICINE Plants have given treatment in customary pharmaceutical frameworks for a long time prior sometime recently the starting of modern pharmaceuticals and more than 70% of people in all of the nation still depend upon conventional medication frameworks15. The current assessment recommended that quite a lot of 1000 plant species in various civilizations have been utilized as medicine, in a simple form of raw materials plants. By tradition, outstanding to their adaptability and accessibility Acacia has a very long historic period16. It is reported that antique Egyptian development used enormous forms of Acacia species (e.g., Acacia bivenosa) to treat various diseases like cancer, asthma, fungal infections, diabetes, and skin diseases. Approximately 80% of Acacia species are native to the U.S.17-19. The present review showed that in the region of 60% of Acacia commonly used in America and Asia Table -1 summarizes the majority of significant applications of Acacia in ethnomedicine. The bark of Acacia salicina is used by local Australian civilization as Antiallergic medicine, to stop bleeding after childbirth, and as a pesticide for poisoning fish. While, in Tunisia, fresh and dried leaves of Acacia arabica plants are used in the healing of cancer, inflammation, and infertility. A different example is the Acacia nilotica evergreen plants which immerse a top position in established medicine in lots of countries. It is extensively found in America, from Senegal to Africa and in Asia20. Although Acacia nilotica has only some frequent traditional uses (in the treatment of diabetes, malaria, wound healing, and cough) in different cultures, Acacia nilotica is utilized commonly against jungle fever in Africa, but ordinarily, it isn't broad in Asia21. Acacia nilotica is utilized commonly against intestinal sickness in Africa, but expectedly it isn't broad in Asia. Out of the 360 species of acacia found in Australia, a little number of Acacia species have been utilized by unique Australians in their conventional pharmaceutical as of now. Acacia was for the foremost portion utilized as a food and flavor enhancer22. There are reports on the use of Acacia species (e.g. Acacia farnesiana, Acacia mellifera, Acacia bivenosa, Acacia moltisimma, Acacia raddiana, Acacia nigrescens, Acacia ixiophylla, Acacia melanoxylon, Acacia gerrardii, Acacia suma, Acacia pyrifolia, Acacia aroma, Acacia nilotica) has been used for treating fever, cold, diarrhea, dysentery and wound healing. Other species such as Acacia aroma, Acacia catechu, and Acacia induxifolia have been reported for their use in the treatment of CVS disease, leprosy, rheumatism, stomach disorder, asthma, cancer, and diabetes23-25. Table 1: Ethnomedicinal uses of Acacia Species Species Acacia adsurgens Acacia albida Delile Parts Used Pods, Bark Gum Region Rumania Kenya Acacia aneura Benth. Acacia arabica Acacia aroma Gillis Roots Leaf Stem, bark Africa India Australia Acacia asak Acacia bivenosa Acacia catechu Acacia caesia Willd. Yemen Brazil Pakistan, India India Acacia colei Maslin Acacia concinna Stem cortex Pods Stem, pods Gum, root, leaf Stem Gum, stem Acacia confuse Acacia cornigera Leaf Bark Taiwan Central America Acacia cuthbertsonii Acacia decurrens Acacia dictyophleba Acacia Karroo Hayne Philippines China Srilanka Southern Africa Acacia leucophloea Seeds Bark Pods Stem, root, bark Bark Acacia mellifera Acacia oxyphylla Acacia pennatula Acacia pennivenia Acacia pruinocarpa Acacia suma Bark Bark Pods Leaf Bark Bark, leaf Bangladesh, Burma, India, Pakistan, SriLanka, Thailand Africa India Pakistan Yemen Africa India Acacia tenuissima Leaf Australia Afghanistan Brazil, U.S Traditional Uses Gastroprotective, used in ophthalmic preparations26 The bark is used in the healing of resting conditions of cattle malaria and is helpful to prevent difficult delivery 27-28. Antipyretic action, anthelmintic, is also used in cough and cold29. Astringent, diarrhea, and dysentery30. Stem and bark showing the activity against arthritis, diuretics use. Also used in the treatment of wound healing, GIT disorders, and antiseptic31. Peptic ulcer, antifungal, and skin diseases32. Antidysentric, used in treatment for gastric distresses33. Treatment against fungal infections, dentifrices34. Treatment of hyperglycemia and externally for allergic reactions35. Used as antidandruff, astringent36. Stem concoction is taken orally for the treatment of cough and used as antimalarial37. The fluid of leaf extract used for wound healing38. Percolation, infusions, decoction, Baths, are used for anti-inflammatory effect39. Treatment of cold, cough, fever and used as mouthwashes40. Bark has been utilized for the treatment of dysentery 41. Used in the treatment of diarrhea, antifungal42. Used for cough and cold wound healing, treatment of syphilis43. The bark is used as anthelmintic, antidiarrhea, expectorant, ulcer healing, heavy bleeding, antiamoebic, treat snake poison, antiallergic44. Used for the treatment of asthma, cardiotonic, malaria sterility 45. The blend of stem barks is used to treat anthelmintic46. Treat against cardiovascular diseases such as stroke, cardiac arrest47. A semi-solid form of leaf is used for women with mastitis48. The bark is used against migraine49. A dried branch of bark is used for the treatment of cold cough and uterine complaints Juice of leaves is also cures diabetic wound healing50. These plants of the leaf are useful to clean skin for general complains 51. 8 Bibhas Pandit et al. Int. Res. J. Pharm. 2021, 12 (12) Table 2: Compounds present in Acacia species Species Acacia farnesiana Acacia mellifera Acacia catechu Chemical constituents Gallic acid Atranorine (+) Catechin Method of detection MS, UV NMR HPLC-DAD Acacia nilotica Acacia bivenosa Acacia moltisimma Acacia raddiana Acacia nigrescence (+)(-) catechin Albiziine Gallic acid 1,3-Di-O-galloyl-1-4, 6(-)3,4- Dihydroxybenzoic acid UV, GC PC HPLC, GC NMR, MS NMR Acacia ixiophylla Acacia melanoxylon Acacia gerrardii Acacia suma Acacia aroma Acacia galpinii Acacia caffra Acacia Senegal Acacia confuse Acacia deccurens Acacia auriculiformis Catechin α-Amino-β-acetylamiopropionic acid Catechin-3’-O-gallate Gallactocatechin-4,8’ epicatechin Hexadecanoic acid(Palmitic acid) Melacacidine Oleic, linoleic, stearic acid Apigenine-6,8 bis c-β-Glucopyranoside 3,4-Dihydroxybenzoic acid Linolic acid 7,3’,5’-trihydroxy-4’-methoxyflavan-3’glucoside (+) Pinitol Myricetin-galloyl-rhamnose D-Gallactopyranose L- rhamnose Β-D-glycoside Linoleic acid, oleic acid L. arabinose PC PC, NMR NMR, MALDI NMR IR, HPLC, GC PMR NMR PMR MS/MS PC, NMR IR, NMR, UV Pharmacological activities Antidiarrhoeal, antifungal Analgesic Antileprotic, antiasthmatic, antioxidant, antimicrobial Ophthalmic, antidiabetic, Antiasthmatic Antidermatitis, antiallergic Anti-inflammatory, antiseptic Antioxidant Antifungal, anti-inflammatory, antiseptic Analgesic, antibacterial Antiarrthritic, antioxidant Antibacterial Antibacterial, Antifluenza Antiinflammatory, antibacterial Astringent, antifungal Antiseptic, Antidermatitis Antidiarrhoeal, antibacterial, ophthalmic Antibacterial, antidiabetic Antiamoebic Antidiabetic TOF, MS HPLC DAD PMR MALDI MS/MS IR, NMR PMR Antiarrthritic, antioxidant Antidiabetic, neuroprotective Antihypertensive Antibacterial, Antiallergic Analgesic Antiasthmatic, antioxidant Antihyperglycemic Acacia mearnsii Acacia pycnantha Acacia deanoi Acacia doratoxylon Acacia implexa Acacia verniciflua Acacia modesta Fig. 1: Different chemical structures in Acacia arabica plant 9 Bibhas Pandit et al. Int. Res. J. Pharm. 2021, 12 (12) PHYTOCHEMISTRY This plant makes raised a variety of auxiliary metabolites. Acacia species are an affluent asset of bioactive compounds counting greasy acids, phenol, alkaloids, polysaccharides, terpenoids, saponins, nonprotein amines, and different natural acids. Current propels in the chromatographic division have revolutionized phytochemical tests for novel bioactive compounds52. The determination of phytoconstituents was from paper, thin-layer chromatography, and high-performance column chromatography, e.g. (HPLC) execution fluid chromatography and (GC) Gas chromatography, has worthy a more exact and total examination of plant extracts. Online spectroscopic methods combining chromatographic procedures such as photodiode cluster location (PDA) and mass spectroscopy (MS) with high-performance chromatography have produced an opulence of static information that has allowed less demanding acknowledgment of Phytochemical. Combination of the high-resolution quadrupole time of flight (Q-TOF) mass spectrometer with HPLC opens the phenomenal potential for the assurance of phytochemical constituents in plant extracts53-54. Plant phenols The main bioactive constituents of plant phenols represent the major group of secondary plant metabolites with worldwide occurrence in the plant kingdom. Though “polyphenols” most frequently term used to explain plant phenols in the literature, the prefix “poly” gives an incorrect thought and seems to prohibit many uncomplicated phenols. Hence, the term “Biophenols” seems to be a more accurate and inclusive explanation of this class of plant secondary metabolites. An assortment of phenolic subclasses that have been recognized in Acacia is phenolic acids, flavonoids, and tannins 48. condensed tannin gallactocatechin-4,8'-epicatechin58. Acacia galpinii and Acacia caffra contain 1,3-Di-O-galloyl-1-4,6(-)oxidisable. Condensed tannins were also recognized in Acacia F. verniciflua 59. Amines and alkaloids These are found in leaves, pods, flower, bark, and roots of Acacia α-Amino-β-acetylamino propionic acid both been reported in subgenus Acacia melanoxylon (e.g., Acacia caesia Nmethyltyramine was also reported in the Phyllodineae which is possibly the most deliberate species in subgenus Acacia melanoxylon contains amines such as tyramine N-methyltyramine N-methyl-b-phenethylamine hordenine and alkaloids including amphetamine methylamphetamine nicotine and nor-nicotine60. PHARMACOLOGY Current and established approaches to healthcare often continue living side by side, in a harmonizing technique. Ethno curative practices have become renowned tools in the look for new pharmaceuticals. In recent times, there has been rehabilitated attention in evaluating plant constituents for their pharmacological activity and to monitoring for successful and safe Phytochemical61. Diverse acacia species have been useful in traditional medicine for an extensive range of ailments (e.g., asthma, fungal infections, diabetes, skin diseases, leprosy, rheumatism, stomach disorder, cancer, dysmenorrheal, eczema, malaria, gout, jaundice, abdominal pain, kidney problems, constipation, piles, pneumonia) Various in vitro and in vivo pharmacological activities of acacia species such as antiinflammatory, antiviral (including HIV infection), antimicrobial, antioxidant, anticancer, antidiabetic, immunomodulatory, hepatoprotective, cardioprotective, and anthelmintic effects are mentioned below62-64. Phenolic acids Analgesic, anti-Inflammatory, and antipyretic activities Phenolic acids are once in a while reported in their complementary and conjugated shapes in Acacia Hydroxyl derivative of cinnamic acids (e.g., ferulic acid) and hydroxyl benzoic acids [e.g., Gallic and syringic acid] both have been acknowledged in these plants. Acacia presents highly phenolic acids were found to be Gallic acid derivatives. The majority of phenol acids have been distinguished within the cases. Amazingly a little sum of phenolic acids was found in leaf or bark. Gallic acid was measured as it were in pods and the concentration wellspring to be extended from 44 to 105 mg/g dry weight of Gallic corrosive in cases. This was various times higher than for seeds55. Tannins Acacia species are the along these lines most bountiful compounds after flavonoids additionally hydrolyzable and condensed tannins (proanthocyanadins). They have been recognized and disconnected from assorted parts of several species. Proanthocyanadins are the most self-evident sort of tannins in Acacia Proanthocyanadins dimmers are standard in Australian species with 6,20,50-trihydroxy substitution is most common but the 6,7,40- trihydroxy-teracacidin bunch is extraordinary in Australian species [56]. Bark extricate of Acacia mearnsii is the world's most extreme yielding source of elevated quality condensed tannins. Due to its tannin constituent and this species of bark may be a significant renewable industrialized source of normal polymers for cement fabricating. It is one of the foremost worldwide tannins make species in Brazil. The extracts comprise catechin, epigallocatechin, oleic, linoleic, stearic acid severed from Acacia caffra, Acacia suma bark extricate contains Inflammation is a complex biological harmful stimulus usual physiological reaction to injury. Anti-inflammatory drugs are among the major highly prescribed and the most supply over-thecounter medications globally. Toxicity and unfavorable reaction to these drugs have always been the main distress, more than ever for continual users65. Biophenols isolated from plants are recognized to alter the creation of (COX) cyclooxygenase and (LOX) lipoxygenase, thus inhibiting bradykinin, prostaglandins, and leukotriene production, correspondingly. These enzymes inhibition generally results in analgesic, anti-inflammatory, and antipyretic activities. The literature showed that analgesic actions of diverse acacia species have been evaluated using chemical (e.g. formalin) or mechanical stimuli (stress and high temperature). Paw edema volume amount is common in animal tests wherever inflammation is induced by egg yolk, dextran, albumin, or carrageenan. Adding together, anti-inflammatory activities can be evaluated without using animals e.g. enzyme inhibition assays of NFⱪβ, cyclooxygenase, or lipoxygenase. For example, Acacia gerardiana (pods), Acacia catechu (pod, leaf, and root bark)66. Acacia confuses (leaf and bark), Acacia modesta (leaf), Acacia vernisiflua (seed), and Acacia doratoxylon (root) produced an analgesic effect in sensitive inflammatory processes while they were introduced to diverse animal models. Acacia suma leaf extract behaved equally to non-steroidal antiinflammatory drugs (NSAIDs). Furthermore, Acacia aroma pods showed an extra prominent result on response time than aspirin. Acacia modesta flower also exhibited analgesic properties which were established with multiple in vitro assays. Acacia suma, Acacia galpinii, and Acacia bivenosa extracts (leaf and bark) showed anti-inflammatory activities by inhibiting a variety of 10 Bibhas Pandit et al. Int. Res. J. Pharm. 2021, 12 (12) inflammatory mediators (leukotriene, histamine, serotonin, bradykinin, and prostaglandin). Additionally, Acacia moltisimma extract was introduced in animal models of anti-inflammatory activity against continual inflammation67. Suppressing the activity of cyclooxygenase enzymes lowers allergic reaction, pain, and inflammation, among various Acacia species showing high-quality action against the enzymes. The pods, roots, and leaf extracts of Acacia senegal and Acacia modesta are reported as showing inhibitory results against both cyclooxygenase 1, 2 respectively. The main effective cyclooxygenase-1 inhibitory response is followed by Acacia suma (leaf) and Acacia bivenosa (stem) extracts68. In vitro COX-1 and COX-2 activity were performed for Acacia aroma (pods, bark, leaf, root, and twig) extracts. Ethanol pods and roots extracts of Acacia aroma infatuated tough activity against both COX-1 and COX-2 discriminating inhibitory activity on COX-2 are superior by the pharmaceutical industry due to their minor toxicity on the gastrointestinal tract. Ironically, many COX-2 inhibitors can boost cardiovascular adverse effects69. Thus, medicinal plants that show COX-2 inhibitory apparent should be clinically assessed for cardiovascular safety70. This test was conceded out for Acacia moltisimma seed extracts in Wister rat polymorph nuclear leukocytes (PMNs), which impart a crucial role in the premature inflammatory response and protection of the host cell against bacterial infection71. The protection of a 500 mg daily dose of Flavocoxid, (a prescription medicinal supplement for osteoarthritis that is prepared from an original blend of flavonoids from Acacia galpinii root and Acacia nilotica bark reported for in vitro COX and LOX inhibitory activities shown in Fig. 2) in patients diagnosed with reasonable knee osteoarthritis was confirmed. Though, there is only one clinical trial that examined the effectiveness of this medicinal supplement. Flavocoxid was found to decrease the physical symptoms linked with knee osteoarthritis in a double-blind randomized prohibited examination using 253 volunteers diagnosed with low-to-me osteoarthritis72. Naproxen (440 mg/day) was used and the clinical results of the botanical mixture were similar with or even greater to naproxen. Fever is regarded as an element of the acute-phase reaction to infection or inflammation73. Acacia nilotica extracts which lowered body temperature and Acacia catechu extract considerably decreased rectal temperature in yeast-induced pyrexia rats as an effect of inhibition of COX or LOX by Acacia flavonoids74. In several cases, chemical compound detection is based on general phytochemical selection, but there is no sign of the active compounds liable for pharmacological activity. Bioactivity-guided fractionation is a significant field that is underutilized for unusual acacia species in treating inflammation, pain, and fever. Fig. 2: Anti-inflammatory mechanism of acacia species Cardiovascular and renal activities WHO reported that more than 18 million people pass away from these diseases each one year. Numerous herbal medicines have been used to cure cardiovascular diseases75. Chemical constituents of Acacia nilotica extracts have been evaluated to their possible mechanism of action: diuretic effects, angiotensinogen converting enzyme (ACE) inhibition, and angiotensinogen receptor blocking (ARB). Six epigallactopyranose were isolated from Acacia nilotica leaf extracts and evaluated against ACE76. Acacia catechu bark extracts were assessed against Swiss albino mice to examine urine volume concentration for Antidiuretic activity77. Indifference, any other supplementing diet with fiber exclusively from acacia gum no response of noteworthy changes in lipid profile ratio in the blood. Newly, a mixture of Acacia gum (20 mg) and hydrocortisone (30 mg) daily for 3 weeks appreciably lower the overall cholesterol, triglycerides, and LDL plasma levels in patients with hypolipidemia78. Antiulcer activities Acacia gerardiana and the roots of Acacia catechu both herbal extracts showed antiulcer and gastroprotective properties in animal model experiments. Acacia gum established the higher gastro reflective properties against the toxic effects of analgesics and anti-inflammatory drugs. Simple leaf extract of Acacia catechu suppresses the release of gastric hydrochloric acid and protected against the inner mucosal layer of GIT. The extract containing more Biophenols showed higher antiulcer activity79. Antioxidant activity In several years, natural antioxidants have to turn into the first preference of scientists, manufacturers, and customers. Free radicals (ROS), Reactive oxygen species are generated in different pathological and physiological works in mammalian systems80. Overproduction of RONS has been linked to cellular aging, damage, pathogenesis, and death. With the virtue of their outstanding antioxidant features, Biophenols are anticipated to play a role in maintaining health and combating diseases. Biophenols can also prevent the rancidity of vegetable oils, slow down the toxic oxidation of food products, enhance shelf life, and main prominently, preserve dietary value81. Antiprotozoal and antimalarial activity In recent times, extensive consideration has been compensated to utilizing ecologically and biologically plant-based yield for controlling parasite infestation. Plants, or their extracts, used to manage protozoan parasites have been widely reviewed82. Acacia has an elongated experimental and traditional history against protozoa: Entamoeba histolytica (causing the gastrointestinal infection), Plasmodium falciparum (causing malaria), and Trypanosoma brucei (causing sleeping sickness). Malaria is the main problem in Australia and 70% of malaria deaths (one million people per year) happen in just 13 Australian countries. To the African, cinchona (Cinchona officinalis, family Rubiaceae) bark was the single identified antimalarial mediator up to the 20th century but a theatrical recrudescence of malaria is continuing due to the progressive drug conflict of the parasite, mainly P. falciparum [83]. Thus, novel compounds with original structures and modes of action diverse to those of the present antimalarial drugs are needed. Conventionally, acacia species have healthy recognized evidence against malaria however additional wide investigational examination is necessary. The whole pods and pods coat (aqueous and methanol), leaf (aqueous), root, and bark (ethanol) extracts of Acacia confusa were assayed for antimalarial 11 Bibhas Pandit et al. Int. Res. J. Pharm. 2021, 12 (12) activity, in vitro, and in vivo, both using Plasmodium berghei or P. falciparum parasites. All parts of the plant gave suitable results, with entire pods and pods coat presentation the most hopeful responses. These data supported the conventional use of this class against malaria84. Anti-hypertensive activity and vasoconstriction activity An ethanol extract of Acacia catechu pods caused a dosage subordinate (2-20mg/kg) drop in arterial blood pressure. The behavior of creatures with atropine nullified the vasodilator response of acetylcholine (ACH), whereas the antihypertensive impact of the plant extricates remained unaltered. Phentolamine (α-adrenergic blocker) abolished neither vasoconstrictor effect of norepinephrine (NE), but pretreatment of the animal with AC, did not alter the NE reaction. These outcomes specify that the antihypertensive effect of plant extract is free of muscarinic receptor stimulus or adrenoreceptor blockade85. Anti-thrombotic activity A revision was accepted by Bukhtiar H. Shah et al that the extract of Acacia bivenosa (Acacia bivenosa) can block platelet aggregation mediated by platelet agonists, ADP (4.3 μM), arachidonic acid (0.75 μM), platelet activate factor (600 nM), and collagen (628 nM) in a dose-dependent manner. The result exposed that the antiplatelet aggregator's action of the extract of Acacia bivenosa is mostly appropriate blockade of Ca2+ channels, even though confirmation also suggests that the participation of protein kinase86-87. CONCLUSION The utilization of homegrown drugs for the anticipation and treatment of different wellbeing afflictions has been in hone from time immemorial. Acacia arabica has been detailed to be compelling against an assortment of malady counting diabetes, skin illness, and most concerning with cancer. The plant's parts of Acacia arabica are considered as an astringent, demulcent, love potion, anthelmintic, antimicrobial, antidiarrheal, with great dietary esteem in the Indian conventional medication framework. This article briefly surveys the ethnobotanical as well as restorative employments of Acacia arabica with plant portrayal. This can be an endeavor to compile and record data on the distinctive angle of Acacia arabica and its potential utility. More ponders have required some time recently the pharmacological properties of Acacia arabica can be utilized in treatment. REFERENCES 1. Kiran Bargali and S.S. Bargali. Acacia nilotica: a multipurpose leguminous plant. Nat Sci. 2009;7(4):12-42. Available from: https://www.semanticscholar.org/paper/ Acacia-nilotica%3A-a-multipurpose-leguminous-plantBargali/3ecd46bdc4c8fabba53ba4cc3afec3a5dc583586 2. Bostock J, Riley TH. The natural history. Somerville, MA: Perseus Digital Library;1855. p. 29-31. Available from: http://www.perseus.tufts.edu/cgi-bin/ptext? lookup=Plin.+Nat.+toc. 3. Agunu A, Yusuf S, Andrew GO, Zezi AU, Abdurahman EM. Evaluation of five medicinal plants used in diarrhea treatment in Nigeria. J Ethnopharmacol. 2005;101(1-3):2730. https://doi.org/10.1016/j.jep.2005.03.025 4. Becker H. Plants for Medicines. A Chemical and Pharmacological Survey of Plants in the Australian Region, East Melbourne: CSIRO Publications;1990. p. 221-225 Available from: https://onlinelibrary.wiley.com/doi/10.1002/ ange.19921040141 5. Subhan N, Burrows GE, Kerr PG, Obied HK. Phytochemistry, Ethnomedicine, and Pharmacology of Acacia. In: Studies in Natural Products Chemistry. 2018. p. 247-326. Available from: https://linkinghub.elsevier.com /retrieve/pii/B9780444640574000090 6. Pennacchio M, Kemp AS. Interesting biological activities from plants traditionally used by native Australians. J. Ethnopharmacol. 2005;96(3):597-601. https://doi.org/ 10.1016/j.jep.2004.10.012 7. Ogunbinu AO, Okeniyi S, Flamini G, Cioni PL, Ogunwande IA, Babalola IT. Essential oil composition of acacia nilotica linn., and acacia albida delile (leguminosae) from nigeria. J Essent Oil Res. 2010;22(6):540-542. Available from: http://www.tandfonline.com/doi/abs/10.1080/10412905.201 0.9700394 8. Venkateshwarlu G, Anasuri S. Traditional and Folklore use of Acacia nilotica (L.) in Ayurvedic System. Asian J. Pharm. Tech. 2014; 4(2):98-99. Available from: https://ajptonline.com/AbstractView.aspx?PID=2014-4-2-9 9. Maslin BR, Miller JT, Seigler DS. Overview of the generic status of Acacia (Leguminosae: Mimosoideae). Australian Systematic Botany. 2003;16. p. 1-18. Available from: http://www.publish.csiro.au/?paper=SB02008 10. Gadilohar NR, Girase A M. A Descriptive Study of Acacia nilotica Linn. Asian. J. Pharm. Res. 2018; 8(3): 170-174. https://doi.org/10.5958/2231-5691.2018.00030.8 11. Subhan N. Phytochemical and pharmacological investigations of Australian Acacia : An ethnomedicineguided bioprospective approach. Dr Philos Charles Sturt Univ. 2016;(March). Available from: https://researchoutput. csu.edu.au/files/9318404/88453 12. Impson F, Hoffmann JH, Kleinjan C. Australian Acacia species (Mimosaceae) in South Africa. In: Muniappan R, Reddy GVP, Raman A, editors. Biological Control of Tropical Weeds Using Arthropods. Cambridge: Cambridge University Press; 2009. p. 38-62. Available from: https://www.cambridge.org/core/product/identifier/CBO978 0511576348A011/type/book_part 13. Ono MA, Wesly G. Black wattle insect pests currently in Brazil. Adv. Res. J. Agric. Sci. 2014;3(12):409-414. Available from: https://www.academia.edu/11719374/ Black_wattle_insect_pests_currently_in_Brazil 14. Venkataswamy R, Doss A. Phytochemical, HPTLC fingerprinting and antibacterial activity of Acacia nilotica (L.) Delile. Hygeia J. D. Med. 2010; 2(2):38–42. Available from: http://www.hygeiajournal.com/Downloads/21227161952231,garima%20new.pdf 15. Harbard JL, Griffin AR, Foster S, Brooker C, Kha LD, Koutoulis A. Production of colchicine-induced autotetraploids as a basis for sterility breeding in Acacia mangium Willd. Forestry: An International J. Forest Res. 2012;85(3):427-36. Available from: https://academic.oup. com/forestry/article/85/3/427/2756050 16. Kusano R, Ogawa S, Matsuo Y, Tanaka T, Yazaki Y, Kouno I. α-amylase and lipase inhibitory activity and structural characterization of acacia bark proanthocyanidins. J. Nat. Prod. 2011;74(2):119-28. Available from: https:// pubs.acs.org/doi/10.1021/np100372t 17. Miller JT, Seigler D. Evolutionary and taxonomic relationships of Acacia. (Leguminosae: Mimosoideae). Vol. 25, Australian Systematic Botany. 2012. p. 217–224. Available from: http://www.publish.csiro.au/?paper= SB11042 18. Meenambiga SS, Rajagopal K. Biofilm inhibition efficiency of endophytic fungi isolated from Acacia nilotica against oral pathogens. Res. J. Pharm. Technol. 2018;11(5):1855-1859. Available from: http://www.indianjournals.com/ijor.aspx? target=ijor:rjpt&volume=11&issue=5&article=030 12 Bibhas Pandit et al. Int. Res. J. Pharm. 2021, 12 (12) 19. Patil S, Naik SR, Joshi V, Jolly CI, Narayanan S. Res. J. Pharmacol. Pharmacodynamics. 2009;1(1):31-34. Available on: https://rjppd.org/AbstractView.aspx?PID=2009-1-1-16 20. Murphy DJ. A review of the classification of Acacia (Leguminosae, Mimosoideae). Vol. 26, Muelleria. 2008. p. 10–26. Avialbale from: https://www.rbg.vic.gov.au/media/ flrfutb2/muelleria_26-1-_p10-26-_murphy_review_classification_acacia.pdf 21. Orchard AE, Maslin BR. The case for conserving Acacia with a new type. Taxon. 2005;54(2):509-512. Available from: https://onlinelibrary.wiley.com/doi/abs/10.2307/25065384 22. McNeill J, Turland NJ. Major changes to the code of nomenclature-Melbourne, July 2011. Taxon. 2011;60(5):1495-1497. Available from: https://onlinelibrary. wiley.com/doi/10.1002/tax.605030 23. Nielsen TRH, Kuete V, Jäger AK, Meyer JJM, Lall N. Antimicrobial activity of selected South African medicinal plants. BMC Complement Altern. Med. 2012;12(1):74. Available from: https://bmccomplementalternmed. biomedcentral.com/articles/10.1186/1472-6882-12-74 24. Karwani G, Singhvi IJ. Gupta SK. Wound Healing Activity of Hydroalcoholic Extract of Acacia catechu. Res. J. Pharm. Tech. 2011;4(6):905-906. Available from: https://rjptonline. org/HTMLPaper.aspx?Journal=Research%20Journal%20of %20Pharmacy%20and%20Technology;PID=2011-4-6-2 25. Smita T, Samrana BR, Ali GMS. Preliminary phytochemical screening and anthelmintic activity of Acacia sinuata (Lourr.) Merr. against intestinal helminthiasis. Res. J. Pharm. Technol. 2011;4(5):756-758. Available from: https:// rjptonline.org/HTMLPaper.aspx?Journal=Research%20Jour nal%20of%20Pharmacy%20and%20Technology;PID=20114-6-2 26. Gadir SA. Assessment of bioactivity of some Sudanese medicinal plants using brine shrimp (Artemia salina) lethality assay. J. Chem. Pharm. Res. 2012;4(12):5145-5148. Available from: https://www.jocpr.com/articles/Assessmentof-bioactivity-of-some-sudanese-medicinal-plants-usingbrine-shrimp-artemia-salina-lethality-assay.pdf 27. Li RW, David Lin G, Myers SP, Leach DN. Antiinflammatory activity of Chinese medicinal vine plants. J Ethnopharmacol. 2003;85(1):61-67. Available from: https://linkinghub.elsevier.com/retrieve/pii/S037887410200 3392 28. Van Vuuren SF. Antimicrobial activity of South African medicinal plants. Vol. 119, Journal of Ethnopharmacology. 2008. p. 462-472. Available from: https://linkinghub.elsevier. com/retrieve/pii/S0378874108003012 29. Müller A, Soyano A. Medicine in Ancient Egypt. Gac Med Caracas. 2021;129(3):734-746. Available from: http://saber. ucv.ve/ojs/index.php/rev_gmc/article/view/22895 30. Haggag MY. Herbal medicine in Egypt. Options Mediterr. 2000;55(23):45-55. Available from: http://om.ciheam.org /article.php?IDPDF=CI011062http://www.ciheam.org/%0A http://om.ciheam.org/ 31. Eldeen IMS, Van Heerden FR, Van Staden J. Biological activities of cycloart-23-ene-3,25-diol isolated from the leaves of Trichilia dregeana. South African J. Bot. 2007;73(3):366-371. Available from: https://linkinghub. elsevier.com/retrieve/pii/S0254629907001998 32. Kala CP, Dhyani PP, Sajwan BS. Developing the medicinal plants sector in northern India: challenges and opportunities. J. Ethnobiol. Ethnomed. 2006;2(1):32. Available from: https://ethnobiomed.biomedcentral.com/articles/10.1186/17 46-4269-2-32 33. Gaikwad JA. Digitisation and analysis of customary medicinal plant knowledge using biodiversity informatics. Macquarie University, Faculty of Science, Department of Chemistry and Biomolecular Sciences; 2011. Available from: 34. 35. 36. 37. 38. 39. 40. 41. 42. 43. 44. 45. 46. https://www.researchgate.net/publication/215756283_Digiti sation_and_analysis_of_customary_medicinal_plant_knowl edge_using_biodiversity_informatics Arias M, Gomez J, Cudmani N, Vattuone M, Isla M. Antibacterial activity of ethanolic and aqueous extracts of Acacia aroma Gill. Life Sci. 2004;75(2):191-202. Available from: https://linkinghub.elsevier.com/retrieve/pii/ S002432050400222X William CJ. Medicinal plants in Australia: v.2: Gums, resins, tannin and essential oils. Choice Rev. Online. 2011;49(03):1449-1457. Available from: http://choicere views.org/review/10.5860/CHOICE.49-1457 Antonsen S, Ostby RB, Stenstrom Y. Naturally Occurring Cyclobutanes: Their Biological Significance and Synthesis. In: Studies in Natural Products Chemistry. 2018. p.1–40. Available from: https://linkinghub.elsevier.com/retrieve/ pii/B9780444640574000016 Maroyi A. Review of ethnopharmacology and phytochemistry of Acacia ataxacantha. Trop. J. Pharm. Res. 2018;17(11):2301-2308. Available from: https://www.ajol. info/index.php/tjpr/article/view/184727 Kull CA, Rangan H. Acacia exchanges: Wattles, thorn trees, and the study of plant movements. Geoforum. 2008;39(3):1258-1272. Available from: https://linkinghub. elsevier.com/retrieve/pii/S0016718507001510 Clarke PA. The Aboriginal Ethnobotany of the Adelaide Region, South Australia. Trans. R. Soc. South. Aust. 2013;137(1):97-126. Available from: https://www. tandfonline.com/doi/full/10.1080/3721426.2013.10887175 William CJ. Medicinal plants in Australia: v.4: An antipodean apothecary. Australia: Rosenberg Publishing; 2013. p. 47-89. Available from: https://books.google.co.in/books?id= 7eVUAQAAQBAJ&pg=PA47&source=gbs_toc_r&cad=4# v=onepage&q&f=false Khan RA. Natural products chemistry: The emerging trends and prospective goals. Saudi Pharm. J. 2018;26(5):739-753. Available from: https://linkinghub.elsevier.com/retrieve/ pii/S1319016418300392 Adedapo AA, Sofidiya MO, Masika PJ, Afolayan AJ. Antiinflammatory and analgesic activities of the aqueous extract of Acacia karroo stem bark in experimental animals. Basic Clin. Pharmacol. Toxicol. 2008;103(5):397-400. Available from: https://onlinelibrary.wiley.com/doi/10.1111/j.17427843.2008.00317.x Lalitha S, Rajeshwaran K. In vivo Screening of Antibacterial Activity of Acacia mellifera (Leguminosae) on Human Pathogenic Bacteria. Global J. Pharmacol. 2010;4(3):148150. Available from: https://www.idosi.org/gjp/gjp4(3).htm Dasgupta S, Roy B, Venkataswamy M, Giri BR. Effects of Acacia oxyphylla and Securinega virosa on functional characteristics of Raillietina echinobothrida (Phylum: Platyhelminthes; Class: Cestoidea), a poultry cestode parasite. J. Parasit. Dis. 2013;37(1):125–30. Available from: http://link.springer.com/10.1007/s12639-012-0145-9 Alonso-Castro AJ, Villarreal ML, Salazar-Olivo LA, GomezSanchez M, Dominguez F, Garcia-Carranca A. Mexican medicinal plants used for cancer treatment: Pharmacological, phytochemical and ethnobotanical studies. J. Ethnopharmacol. 2011;133(3):945-972. Available from: https://linkinghub.elsevier.com/retrieve/pii/S037887411000 8408 Mothana RA, Lindequist U, Gruenert R, Bednarski PJ. Studies of the in vitro anticancer, antimicrobial and antioxidant potentials of selected Yemeni medicinal plants from the island Soqotra. BMC Complement. Altern. Med. 2009;9(1):7. Available from: https://bmccomple mentalternmed.biomedcentral.com/articles/10.1186/14726882-9-7 13 Bibhas Pandit et al. Int. Res. J. Pharm. 2021, 12 (12) 47. Eldeen IMS, Van Staden J. In vitro pharmacological investigation of extracts from some trees used in Sudanese traditional medicine. South African J. Bot. 2007;73(3):435440. Available from: https://linkinghub.elsevier.com/retrieve /pii/S0254629907002384 48. Agarwal S, Mittal S, Bajaj H, Chauhan B, Kumar R. Pyrexia: pathophysiology and use of herbal drugs. Int. Res. J. Pharm. 2016;7(4):1-8. Available from: http://www.irjponline.com /admin/php/uploads/2476_pdf.pdf 49. Wink M. Evolution of secondary metabolites in legumes (Fabaceae). South African J. Bot. 2013;89:164-175. Available from: https://linkinghub.elsevier.com/ retrieve/pii/S0254629913002858 50. Ganzera M, Sturm S. Recent advances on HPLC/MS in medicinal plant analysis-An update covering 2011–2016. Vol. 147, Journal of Pharmaceutical and Biomedical Analysis. 2018. p. 211–233. Available from: https:// linkinghub.elsevier.com/retrieve/pii/S0731708517312633 51. Obied HK. Biography of biophenols: Past, present and future. Funct. Foods Heal Dis. 2013;3(6):230-241. Available from: https://ffhdj.com/index.php/ffhd/article/view/51 52. Tura D, Robards K. Sample handling strategies for the determination of biophenols in food and plants. J. Chromatogr. A. 2002;975(1):71-93. Available from: https://linkinghub.elsevier.com/retrieve/pii/S002196730200 8798 53. Ee KY, Agboola S, Rehman A, Zhao J. Characterisation of phenolic components present in raw and roasted wattle (Acacia victoriae Bentham) seeds. Food Chem. 2011;129(3):816-821. Available from: https://linkinghub. elsevier.com/retrieve/pii/S0308814611007175 54. Magesh A, Lakshmi T. Preliminary phytochemical analysis of Acacia catechu wild Heartwood extract. Res. J. Pharm. & Tech. 2012; 5(11):1393-1395. Available from: https://rjptonline.org/HTMLPaper.aspx?Journal=Research% 20Journal%20of%20Pharmacy%20and%20Technology;PID =2012-5-11-17 55. Maldini M, Montoro P, Hamed AI, Mahalel UA, Oleszek W, Stochmal A, et al. Strong antioxidant phenolics from Acacia nilotica: Profiling by ESI-MS and qualitative-quantitative determination by LC-ESI-MS. J. Pharm. Biomed. Anal. 2011;56(2):228–39. Available from: https://linkinghub. elsevier.com/retrieve/pii/S0731708511002780 56. Seigler DS. Phytochemistry of Acacia-Sensu lato. In: Biochemical Systematics and Ecology. 2003. p. 845–873. Available from: https://linkinghub.elsevier.com/retrieve /pii/S0305197803000826 57. Ferreira D, Marais JPJ, Slade D. Heterogeneity of the Interflavanyl Bond in Proanthocyanidins from Natural Sources Lacking C-4 (C-Ring) Deoxy Flavonoid Nucleophiles. ChemInform. 2006;37(2). Available from: https://onlinelibrary.wiley.com/doi/10.1002/chin.200602272 58. Hendra R, Willis A, Keller PA. Phytochemical studies on the Australian native plant species Acacia pycnantha and Jacaranda mimosifolia. Nat. Prod. Res. 2019;33(14):19972003. Available from: https://www.tandfonline.com/doi /full/10.1080/14786419.2018.1483922 59. Elmi A, Spina R, Risler A, Philippot S, Mérito A, Duval RE, et al. Evaluation of antioxidant and antibacterial activities, cytotoxicity of acacia seyal del bark extracts and isolated compounds. Molecules. 2020;25(10):2392. Available from: https://www.mdpi.com/1420-3049/25/10/2392 60. Alharbi WDM, Azmat A. Hypoglycemic and hypocholesterolemic affects of Acacia tortillas (Fabaceae) growing in Makkah. Pak. J. Pharmacol. 2011;28:1-8. Available from: https://www.academia.edu/29691719/ hypoglycemic_and_hypocholesterolemic_effects_of_acacia _tortilis_fabaceae_growing_in_makkah 61. Mashour NH, Lin GI, Frishman WH. Herbal medicine for the treatment of cardiovascular disease: Clinical considerations. Vol. 158, Archives of Internal Medicine. 1998. p. 2225-2234. Available from: http://archinte.jamanetwork.com/ article.aspx?doi=10.1001/archinte.158.20.2225 62. Mohan KUS, Viswaroopan D. A review on kumarabharana prasha: a novel ayurvedic electuary. Int. J. Res. Ayurveda Pharm. 2018;9(3):140-1466. Available from: http://www.ijrap.net/admin/php/uploads/2067_pdf.pdf 63. Haskell WL, Spiller GA, Jensen CD, Ellis BK, Gates JE. Role of water-soluble dietary fiber in the management of elevated plasma cholesterol in healthy subjects. Am. J. Cardiol. 1992;69(5):433–9. Available from: https://linkinghub. elsevier.com/retrieve/pii/000291499290980D 64. Aravind KS, Arun AV. Invitro Antibacterial Activity of Acacia catechu ethanolic leaf extract against selected acidogenic oral bacteria. Res. J. Pharm. & Tech. 2012; 5(3):333-336. Available from: https://rjptonline.org /HTMLPaper.aspx?Journal=Research%20Journal%20of%20 Pharmacy%20and%20Technology;PID=2012-5-3-28 65. Acharyya S, Dash GK, Pattnaik S, Chhetree RR. Antihyperglycemic and antihyperlipidemic activity of Acacia suma (Roxb.) barks. Res. J. Pharmacol. and Pharmacodynamics. 2011;3(2):67-71. Available from: https://www.indianjournals.com/ijor.aspx?target=ijor:rjppd &volume=3&issue=2&article=005 66. EI Tobgy K. Protective role of Gum Arabic (Acacia Senegal) on oxidative stress in diabetic and adenine induced chronic renal failure in rats. Int. J. Chem. Tech. Res. 2019;12(01):223-234. Available from: http://sphinxsai.com/ 2019/ch_vol12_no1/2/(223-234)V12N1CT.pdf 67. Jacobson PB, Kuchera SL, Metz A, Schachtele C, Imre K, Schrier DJ. Anti-inflammatory properties of Go 6850: A selective inhibitor of protein kinase-C. J. Pharmacol. Exp. Ther. 1995;275(2):995-1002. Available from: https:// jpet.aspetjournals.org/content/275/2/995.long 68. Arjmandi BH, Ormsbee LT, Elam ML, Campbell SC, Rahnama N, Payton ME, et al. A combination of Scutellaria baicalensis and Acacia catechu extracts for short-term symptomatic relief of joint discomfort associated with osteoarthritis of the knee. J. Med Food. 2014;17(6):707-713. Available from: http://www.liebertpub.com/doi/10.1089 /jmf.2013.0010 69. Antipyretic and analgesic activities of aqueous extract of Acacia nilotica root. Biokemistri. 2015;26(2):55-62. Available from: https://www.ajol.info/index.php/biokem/ article/view/113765 70. Benamar H, Rached W. Screening of Algerian Medicinal Plants for Acetyl cholinesterase Inhibitory Activity. J. Biol Sci. 2010; 10(1):1-9. Available from: https:// docsdrive.com/pdfs/ansinet/jbs/2010/1-9.pdf 71. Atif Ali. Acacia nilotica: A plant of multipurpose medicinal uses. J. Med. Plants Res. 2012;6(9):1492-1496. Available from: https://academicjournals.org/journal/JMPR/articleabstract/4EC523629622 72. Thangavelu L, Ramasamy R. In vitro acetyl cholinesterase inhibitory assay of acacia catechu willd ethanolic seed extract. Pharmacogn J. 2015;7(5):280-282. Available from: http://www.phcogj.com/article/68 73. Hebbar SS, Harsha VH, Shripathi V, Hegde GR. Ethnomedicine of Dharwad district in Karnataka, India Plants used in oral health care. J. Ethnopharmacol. 2004;94(2–3):261-266. Available from: https://linkinghub. elsevier.com/retrieve/pii/S037887410400220X 74. Ndung’u FL, Kaimenyi JT, Arneberg P, Muthami LN. A comparative study of the efficacy of plaque control by a chewing stick and a tooth brush. East Afr. Med. J. 14 Bibhas Pandit et al. Int. Res. J. Pharm. 2021, 12 (12) 75. 76. 77. 78. 79. 80. 81. 82. 1990;67(12):907-911. Available from: https://pubmed. ncbi.nlm.nih.gov/2083526 Pradeep AR, Happy D, Garg G. Short-term clinical effects of commercially available gel containing Acacia arabica: A randomized controlled clinical trial. Aust. Dent. J. 2010;55(1):65-69. Available from: https://onlinelibrary. wiley.com/doi/10.1111/j.1834-7819.2009.01180.x Gazi MI. The finding of antiplaque features in Acacia arabica type of chewing gum. J. Clin. Periodontol. 1991;18(1):75-77. Available from: https://onlinelibrary.wiley.com/doi/ 10.1111/j.1600-051X.1991.tb01123.x Ramli S, Harada KI, Ruangrungsi N. Antioxidant, antimicrobial and cytotoxicity activities of Acacia farnesiana (L.) Willd. leaves ethanolic extract. Pharmacogn. J. 2011;3(23):50-58. Available from: http://linkinghub. elsevier.com/retrieve/pii/S0975357511800830 Al-Mustafa ZH, Dafallah AA. A Study on the toxicology of Acacia nilotica. Am. J. Chin. Med. 2000;28(1):123-129. Available from: https://www.worldscientific.com/doi/ abs/10.1142/S0192415X00000155 David Phillipson J, Wright CW. Can ethnopharmacology contribute to the development of antimalarial agents? J. Ethnopharmacol. 1991;32(1–3):155-165. Available from: https://linkinghub.elsevier.com/retrieve/pii/03788741919011 3R Ravikumar S, Inbaneson SJ, Suganthi P. In vitro antiplasmodial activity of ethanolic extracts of South Indian medicinal plants against Plasmodium falciparum. Asian Pacific J. Trop. Dis. 2012;2(3):180-183. Available from: https://linkinghub.elsevier.com/retrieve/pii/S222218081260 0437 Alli LA, Adesokan AA, Salawu AO. Antimalarial activity of fractions of aqueous extract of Acacia nilotica root. J. Intercult. Ethnopharmacol. 2016;5(2):180-1855. Available from: http://www.scopemed.org/fulltextpdf.php? mno=216788 El-Tahir A, Satti GMH, Khalid SA. Antiplasmodial activity of selected Sudanese medicinal plants with emphasis on 83. 84. 85. 86. 87. Acacia nilotica. Phyther. Res. 1999;13(6):474-478. Available from: https://onlinelibrary.wiley.com/doi/10.1002/(SICI) 1099-1573(199909)13:6%3C474::AID-PTR482%3E3.0.CO; 2-6 Payne SE, Kotze AC, Durmic Z, Vercoe PE. Australian plants show anthelmintic activity toward equine cyathostomins in vitro. Vet. Parasitol. 2013;196(1-2):153-160. Available from: https://linkinghub.elsevier.com/retrieve/pii/S030440171300 037X Lalchhandama K, Roy B, Dutta BK. Anthelmintic activity of Acacia oxyphylla stem bark against Ascaridia galli. Pharm. Biol. 2009;47(7):578-583. Available from: http://www. tandfonline.com/doi/full/10.1080/13880200902902463 Gilani AH, Shaheen F, Zaman M, Janbaz KH, Shah BH, Akhtar MS. Studies on antihypertensive and antispasmodic activities of methanol extract of Acacia nilotica pods. Phyther Res. 1999;13(8):665-669. Available from: https:// onlinelibrary.wiley.com/doi/10.1002/(SICI)10991573(19991 2)13:8%3C665::AID-PTR563%3E3.0.CO;2-T Zaman R, Shamsi S, Zaman R, Itrat M. Bark of Acacia Arabica -A Nature’s Gift: An Overview. Int. Res. J. Med. Sci. 2014;2(5):20-24. Available from: https://www.researchgate. net/publication/332858395_Bark_of_Acacia_Arabica_A_Nature’s_Gift_An_Overview Malviya S. Medicinal attributes of Acacia nilotica Linn- A comprehensive review on ethno-pharmacological claims. Int. J. Pharm. Life Sci. 2011;2(6):830-837. http:// www.ijplsjournal.com/issues%20PDF%20files/june%20201 1/9.pdf Cite this article as: Bibhas Pandit et al. A review on the restorative impact of Acacia arabica. Int. Res. J. Pharm. 2021;12(12):7-15. http://dx.doi.org/10.7897/2230-8407.1212173 Source of support: Nil, Conflict of interest: None Declared Disclaimer: IRJP is solely owned by Moksha Publishing House - A non-profit publishing house, dedicated to publishing quality research, while every effort has been taken to verify the accuracy of the content published in our Journal. IRJP cannot accept any responsibility or liability for the site content and articles published. 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