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Current Drug Therapy

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ISSN (Print): 1574-8855
ISSN (Online): 2212-3903

Review Article

Therapeutic Importance and Pharmacological Activities of Karanjin in the Medicine for the Treatment of Human Disorders: A Review through Scientific Data Analysis

Author(s): Dinesh Kumar Patel* and Kanika Patel

Volume 17, Issue 2, 2022

Published on: 25 May, 2022

Page: [71 - 78] Pages: 8

DOI: 10.2174/1574885517666220307113724

Price: $65

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Abstract

Backgrounds: Plant and derived herbal drugs have been used in the traditional medicine system to treat various human health complications from a very early age. Commercial products prepared from natural herbs have always been valuable for society in the form of health supplements to medicament. In ancient times, herbal products were mainly prepared from plants and derived phytochemicals. Plants contain a rich source of pure phytochemicals called secondary metabolites, and examples are flavonoids, glycosides, tannins, terpenoids, etc. Plants and their parts, including fruits, flowers, vegetables, etc., are the best source of Flavonoid class phytochemicals.

Methods: Present work summarized the scientific information of karanjin for their beneficial health aspects and pharmacological activities, including its analytical aspects. In the present investigation, scientific data on karanjin have been collected from various scientific databases such as Google, Google Scholar, Science Direct, and PubMed and analyzed to know the beneficial health aspects of karanjin in medicine. Further pharmacological activity data has been collected and analyzed in the present work to know their biological potential in medicine. Analytical methods used for the separation, isolation, and identification of karanjin to standardize different natural products have also been discussed in the present work.

Results: Scientific data analysis signified the biological importance of Flavonoid class phytochemicals in the medicine as they are well known for their anti-ischemic, vasodilatory, anti-bacterial, antiinflammatory, anti-oxidant, anti-viral, and anti-cancer activities. Scientific data analysis revealed the presence of karanjin in numerous medicinal plants such as Fordia cauliflora, Lonchocarpus latifolius, Millettia pinnata, Millettia pubinervis, Pongamia pinnata, and Tephrosia purpurea. Pharmacological activity data revealed the biological potential of karanjin against cancerous disorders, glucose metabolism abnormalities, gastrointestinal disorders, arthritis, inflammatory disorders, colitis, psoriasis, and brain-related disorders. However, analytical data signified the importance of RP-HPLC, TLC, HPTLC, UPLC-ESI-MS/MS, and HSCCC techniques in the medicine to quantify karanjin in different samples.

Conclusion: Presented information about karanjin in this review paper will be beneficial to the scientific peoples of the world to know the beneficial health aspects of karanjin in medicine.

Keywords: Karanjin, flavonoid, cancer, glucose metabolism, gastrointestinal disorders, arthritis, inflammatory disorders, colitis, psoriasis, brain disorders.

Graphical Abstract
[1]
Patel K, Kumar V, Rahman M, Verma A, Patel DK. New insights into the medicinal importance, physiological functions and bioanalytical aspects of an important bioactive compound of foods ‘Hyperin’: Health benefits of the past, the present, the future. Beni Suef Univ J Basic Appl Sci 2018; 7(1): 31-42.
[http://dx.doi.org/10.1016/j.bjbas.2017.05.009]
[2]
Patel K, Kumar V, Rahman M, Verma A, Patel DK. Rhamnazin: A systematic review on ethnopharmacology, pharmacology and analytical aspects of an important phytomedicine. Curr Tradit Med 2018; 4(2): 120-7.
[http://dx.doi.org/10.2174/2215083804666180416124949]
[3]
Patel K, Kumar V, Verma A, Rahman M, Patel DK. β-sitosterol: Bioactive compounds in foods, their role in health promotion and disease prevention “a concise report of its phytopharmaceutical importance”. Curr Tradit Med 2017; 3(3): 168-77.
[http://dx.doi.org/10.2174/2215083803666170615111759]
[4]
Patel K, Kumar V, Verma A, Rahman M, Patel DK. Amarogentin as topical anticancer and anti-infective potential: Scope of lipid based vesicular in its effective delivery. Recent Pat Antiinfect Drug Discov 2019; 14(1): 7-15.
[http://dx.doi.org/10.2174/1574891X13666180913154355] [PMID: 30210007]
[5]
Patel K, Patel DK. Medicinal importance, pharmacological activities, and analytical aspects of hispidulin: A concise report. J Tradit Complement Med 2016; 7(3): 360-6.
[http://dx.doi.org/10.1016/j.jtcme.2016.11.003] [PMID: 28725632]
[6]
Patel K, Patel DK. Medicinal significance, pharmacological activities, and analytical aspects of ricinine: A concise report. J Coast Life Med 2016; 4(8): 663-7.
[http://dx.doi.org/10.12980/jclm.4.2016J6-96]
[7]
Patel K, Mishra R, Patel DK. A review on phytopharmaceutical importance of asiaticoside. J Coast Life Med 2016; 4(12): 1000-7.
[http://dx.doi.org/10.12980/jclm.4.2016J6-161]
[8]
Marques GS, Leão WF, Lyra MAM, et al. Comparative evaluation of UV/VIS and HPLC analytical methodologies applied for quantification of flavonoids from leaves of Bauhinia forficata. Rev Bras Farmacogn 2013; 23(1): 51-7.
[http://dx.doi.org/10.1590/S0102-695X2012005000143]
[9]
Pereira DF, Cazarolli LH, Lavado C, et al. Effects of flavonoids on α-glucosidase activity: Potential targets for glucose homeostasis. Nutrition 2011; 27(11-12): 1161-7.
[http://dx.doi.org/10.1016/j.nut.2011.01.008] [PMID: 21684120]
[10]
Morita M, Takahashi I, Kanai M, et al. Baicalein 5,6,7-trimethyl ether, a flavonoid derivative, stimulates fatty acid β-oxidation in skin fibroblasts of X-linked adrenoleukodystrophy. FEBS Lett 2005; 579(2): 409-14.
[http://dx.doi.org/10.1016/j.febslet.2004.11.102] [PMID: 15642351]
[11]
Mohan S, Nandhakumar L. Role of various flavonoids: Hypotheses on novel approach to treat diabetes. J Med Hypotheses Ideas 2014; 8(1): 1-6.
[http://dx.doi.org/10.1016/j.jmhi.2013.06.001]
[12]
De Souza LA, Tavares WMG, Lopes APM, Soeiro MM, De Almeida WB. Structural analysis of flavonoids in solution through DFT 1H NMR chemical shift calculations: Epigallocatechin, Kaempferol and Quercetin. Chem Phys Lett 2017; 676: 46-52.
[http://dx.doi.org/10.1016/j.cplett.2017.03.038]
[13]
Govindarasu M, Palani M, Vaiyapuri M. In silico docking studies on kaempferitrin with diverse inflammatory and apoptotic proteins functional approach towards the colon cancer. Int J Pharm Pharm Sci 2017; 9(9): 199.
[http://dx.doi.org/10.22159/ijpps.2017v9i9.20500]
[14]
Bestwick CS, Milne L, Pirie L, Duthie SJ. The effect of short-term kaempferol exposure on reactive oxygen levels and integrity of human (HL-60) leukaemic cells. Biochim Biophys Acta 2005; 1740(3): 340-9.
[http://dx.doi.org/10.1016/j.bbadis.2004.10.005] [PMID: 15949701]
[15]
Arshad N, Rashid N, Absar S, Abbasi MSA, Saleem S, Mirza B. UV-absorption studies of interaction of karanjin and karanjachromene with ds. DNA: Evaluation of binding and antioxidant activity. Cent Eur J Chem 2013; 11: 2040-7.
[16]
Pandey A, Bajpai AK, Kumar A, Pal M, Baboo V, Dwivedi A. Isolation, identification, molecular and electronic structure, vibrational spectroscopic investigation, and anti-HIV-1 activity of karanjin using density functional theory. J Theor Chem 2014; 2014: 1-13.
[http://dx.doi.org/10.1155/2014/680987]
[17]
Patel PP, Trivedi ND. Simple, efficient and economic method forisolation and analysis of karanjin and pongamol from karanja seed oil and screening of antimicrobial potential. Int J Pharm Pharm Sci 2015; 7: 248-52.
[18]
Sreelakshmi L, Janardhan RK. Detection of karanjin from callus cultures of Pongamia glabra. J Pharmacogn 2012; 3: 67-70.
[19]
Yadav PP, Gupta P, Chaturvedi AK, Shukla PK, Maurya R. Synthesis of 4-hydroxy-1-methylindole and benzo[b]thiophen-4-ol based unnatural flavonoids as new class of antimicrobial agents. Bioorg Med Chem 2005; 13(5): 1497-505.
[http://dx.doi.org/10.1016/j.bmc.2004.12.032] [PMID: 15698765]
[20]
Guo J-R, Chen Q-Q, Lam CW-K, Zhang W. Effects of karanjin on cell cycle arrest and apoptosis in human A549, HepG2 and HL-60 cancer cells. Biol Res 2015; 48(1): 40.
[http://dx.doi.org/10.1186/s40659-015-0031-x] [PMID: 26209237]
[21]
Katekhaye S, Kale MS, Laddha KS. Development and validation of an HPLC method for Karanjin in Pongamia pinnata Linn. Leaves. Indian J Pharm Sci 2012; 74(1): 72-5.
[http://dx.doi.org/10.4103/0250-474X.102547] [PMID: 23204626]
[22]
Shejawal N, Menon S, Shailajan S. Bioavailability of karanjin from Pongamia pinnata L. in Sprague dawley rats using validated RP-HPLC method. J Appl Pharm Sci 2014. 4: 010-4.
[23]
Mrudul V, Pravin T. Investigation of Anti-cancer potential of Karanjin in MCF-7 and MDAMB-231 breast carcinoma cells. Int J Adv Sci Technol 2020; 29: 937-45.
[24]
Soren NM, Sharma AK, Sastry VRB. Biochemical and histopathological changes in sheep fed different detoxified karanj (Pongamia glabra) seed cake as partial protein supplements. Anim Nutr 2017; 3(2): 164-70.
[http://dx.doi.org/10.1016/j.aninu.2017.04.002] [PMID: 29767061]
[25]
Singh A, Bhatt G, Gujre N, et al. Karanjin. Phytochemistry 2021; 183: 112641.
[http://dx.doi.org/10.1016/j.phytochem.2020.112641] [PMID: 33421890]
[26]
Das S, Tiwari GJ, Ghosh A. In silico analysis of new flavonoids from Pongamia pinnata with a therapeutic potential for agerelated macular degeneration. 3 Biotech 2020; 10: 536.
[27]
Majumdar D. Suppression of nitrification and N2O emission by karanjin--a nitrification inhibitor prepared from karanja (Pongamia glabra Vent.). Chemosphere 2002; 47(8): 845-50.
[http://dx.doi.org/10.1016/S0045-6535(01)00287-9] [PMID: 12079079]
[28]
Xue Y, Li H, Zhang Y, et al. Natural and synthetic flavonoids, novel blockers of the volume-regulated anion channels, inhibit endothelial cell proliferation. Pflugers Arch 2018; 470(10): 1473-83.
[http://dx.doi.org/10.1007/s00424-018-2170-8] [PMID: 29961148]
[29]
Joshi P, Sonawane VR, Williams IS, et al. Identification of karanjin isolated from the Indian beech tree as a potent CYP1 enzyme inhibitor with cellular efficacy via screening of a natural product repository. MedChemComm 2018; 9(2): 371-82.
[http://dx.doi.org/10.1039/C7MD00388A] [PMID: 30108931]
[30]
Roy R, Mandal S, Chakrabarti J, Saha P, Panda CK. Downregulation of Hyaluronic acid-CD44 signaling pathway in cervical cancer cell by natural polyphenols Plumbagin, Pongapin and Karanjin. Mol Cell Biochem 2021; 476(10): 3701-9.
[http://dx.doi.org/10.1007/s11010-021-04195-1] [PMID: 34081254]
[31]
Zhang J, Xie Y, Fan Q, Wang C. Effects of karanjin on dimethylhydrazine induced colon carcinoma and aberrant crypt foci are facilitated by alteration of the p53/Bcl2/BAX pathway for apoptosis. Biotech Histochem 2021; 96(3): 202-12.
[http://dx.doi.org/10.1080/10520295.2020.1781258] [PMID: 32580584]
[32]
Roy R, Pal D, Sur S, Mandal S, Saha P, Panda CK. Pongapin and Karanjin, furanoflavanoids of Pongamia pinnata, induce G2/M arrest and apoptosis in cervical cancer cells by differential reactive oxygen species modulation, DNA damage, and nuclear factor kappa-light-chain-enhancer of ac. Phytother Res 2019; 33: 1084-94.
[http://dx.doi.org/10.1002/ptr.6302] [PMID: 30834631]
[33]
Mohd Noor AA, Othman SNN, Lum PT, Mani S, Shaikh MF, Sekar M. Molecules of interest – karanjin – a review. Pharmacogn J 2020; 12(4): 938-45.
[http://dx.doi.org/10.5530/pj.2020.12.133]
[34]
Jaiswal N, Yadav PP, Maurya R, Srivastava AK, Tamrakar AK. Karanjin from Pongamia pinnata induces GLUT4 translocation in skeletal muscle cells in a phosphatidylinositol-3-kinase-independent manner. Eur J Pharmacol 2011; 670(1): 22-8.
[http://dx.doi.org/10.1016/j.ejphar.2011.08.049] [PMID: 21939653]
[35]
Tamrakar AK, Yadav PP, Tiwari P, Maurya R, Srivastava AK. Identification of pongamol and karanjin as lead compounds with antihyperglycemic activity from Pongamia pinnata fruits. J Ethnopharmacol 2008; 118(3): 435-9.
[http://dx.doi.org/10.1016/j.jep.2008.05.008] [PMID: 18572336]
[36]
Mandal B, Maity CR. Hypoglycemic action of karanjin. Acta Physiol Pharmacol Bulg 1986; 12(4): 42-6.
[PMID: 3577798]
[37]
Saini P, Lakshmayya L, Bisht VS. Anti-Alzheimer activity of isolated karanjin from Pongamia pinnata (L.) pierre and embelin from Embelia ribes Burm.f. An Int Q J Res Ayurveda 2017; 38(12): 76-81.
[PMID: 29861598]
[38]
Vismaya BSM. R S, J VB, D SM, T SK. Gastroprotective properties of karanjin from karanja (Pongamia pinnata) Seeds; Role as antioxidant and H, K-ATpase inhibitor. Evid Based Complement Altern Med 2011; 747246.
[39]
Bose M, Chakraborty M, Bhattacharya S, Mukherjee D, Mandal S, Mishra R. Prevention of arthritis markers in experimental animal and inflammation signalling in macrophage by Karanjin isolated from Pongamia pinnata seed extract. Phytother Res 2014; 28(8): 1188-95.
[http://dx.doi.org/10.1002/ptr.5113] [PMID: 24399783]
[40]
Patel PP, Trivedi ND. Effect of karanjin on 2,4,6-trinitrobenzenesulfonic acid-induced colitis in Balb/c mice. Indian J Pharmacol 2017; 49(2): 161-7.
[PMID: 28706329]
[41]
Ghosh A, Tiwari GJ. Role of nitric oxide-scavenging activity of Karanjin and Pongapin in the treatment of Psoriasis. 3 Biotech 2018; 8: 338.
[42]
Ansari SA, Qadir A, Warsi MH, et al. Ethosomes-based gel formulation of karanjin for treatment of acne vulgaris: In vitro investigations and preclinical assessment. 3 Biotech 2021; 11(11): 456.
[43]
Rekha MJ, Bettadaiah BK, Muthukumar SP, Govindaraju K. Synthesis, characterization and anti-inflammatory properties of karanjin (Pongamia pinnata seed) and its derivatives. Bioorg Chem 2021; 106: 104471.
[http://dx.doi.org/10.1016/j.bioorg.2020.104471] [PMID: 33257003]
[44]
Perumalsamy H, Jang MJ, Kim J-R, Kadarkarai M, Ahn Y-J. Larvicidal activity and possible mode of action of four flavonoids and two fatty acids identified in Millettia pinnata seed toward three mosquito species. Parasit Vectors 2015; 8(1): 237.
[http://dx.doi.org/10.1186/s13071-015-0848-8] [PMID: 25928224]
[45]
Raghav D, Mahanty S, Rathinasamy K. Biochemical and toxicological investigation of karanjin, a bio-pesticide isolated from Pongamia seed oil. Pestic Biochem Physiol 2019; 157: 108-21.
[http://dx.doi.org/10.1016/j.pestbp.2019.03.011] [PMID: 31153458]
[46]
Ribeiro LP, Zanardi OZ, Vendramim JD, Yamamoto PT. Comparative toxicity of an acetogenin-based extract and commercial pesticides against citrus red mite. Exp Appl Acarol 2014; 64(1): 87-98.
[http://dx.doi.org/10.1007/s10493-014-9810-2] [PMID: 24696362]
[47]
Michaelis M, Rothweiler F, Nerreter T, Sharifi M, Ghafourian T, Cinatl J. Karanjin interferes with ABCB1, ABCC1, and ABCG2. J Pharm Pharm Sci 2014; 17(1): 92-105.
[http://dx.doi.org/10.18433/J3BW2S] [PMID: 24735762]
[48]
Yi D, Wang Z, Yi L. Development and validation of an LC-MS method for determination of Karanjin in rat plasma: Application to preclinical pharmacokinetics. J Chromatogr Sci 2015; 53(4): 456-61.
[http://dx.doi.org/10.1093/chromsci/bmu064] [PMID: 25002684]
[49]
Kumar G, Gupta R, Sharan S, Roy P, Pandey DM. Anticancer activity of plant leaves extract collected from a tribal region of India. 3 Biotech 2019; 9: 399.
[50]
Peng Y, Chen Y, Gao C, Yan T, Cao W, Huang R. A new 1,2-ethanedione benzofurane derivative from Tephrosia purpurea. Nat Prod Res 2014; 28(20): 1705-8.
[http://dx.doi.org/10.1080/14786419.2014.940587] [PMID: 25116833]
[51]
Yin H, Zhang S, Wu J. Study on flavonoids from stem bark of Pongamia pinnata. Zhong Yao Cai 2004; 27(7): 493-5.
[PMID: 15551964]
[52]
Simin K, Ali Z, Khaliq-Uz-Zaman SM, Ahmad VU. Structure and biological activity of a new rotenoid from Pongamia pinnata. Nat Prod Lett 2002; 16(5): 351-7.
[http://dx.doi.org/10.1080/10575630290033114] [PMID: 12434992]
[53]
Na Z, Song Q-S, Hu H-B. Flavonoids from twigs of Millettia pubinervis. Nat Prod Commun 2014; 9: 1934578X1400901.
[http://dx.doi.org/10.1177/1934578X1400901214]
[54]
Magalhães AF, Tozzi AMA, Magalhães EG, Nogueira MA, Queiroz SCN. Flavonoids from Lonchocarpus latifolius roots. Phytochemistry 2000; 55(7): 787-92.
[http://dx.doi.org/10.1016/S0031-9422(00)00300-9] [PMID: 11190397]
[55]
Ahmad G, Mishra PK, Gupta P, et al. Synthesis of novel benzofuran isoxazolines as protein tyrosine phosphatase 1B inhibitors. Bioorg Med Chem Lett 2006; 16(8): 2139-43.
[http://dx.doi.org/10.1016/j.bmcl.2006.01.062] [PMID: 16460930]
[56]
Liang ZY, Yang XS, Zhu HY, Hao XJ. Two new flavones from Fordia cauliflora of Yunnan. Yao Xue Xue Bao 2006; 41(6): 533-6.
[PMID: 16927828]
[57]
Yin H, Zhang S, Long L, et al. The separation of flavonoids from Pongamia pinnata using combination columns in high-speed counter-current chromatography with a three-phase solvent system. J Chromatogr A 2013; 1315: 80-5.
[http://dx.doi.org/10.1016/j.chroma.2013.09.010] [PMID: 24090596]
[58]
Ghosh A, Mandal S, Banerji A, Kar M, Banerji J. A new chalcone from Pongamia pinnata and its antioxidant properties. Nat Prod Commun 2009; 4: 1934578X0900400.
[http://dx.doi.org/10.1177/1934578X0900400207]
[59]
Vo T-H, Liaw C-C, Lin Y-C, et al. Quantification and optimization of ethanolic extract containing the bioactive flavonoids from Millettia pulchra radix. Molecules 2021; 26(12): 3641.
[http://dx.doi.org/10.3390/molecules26123641] [PMID: 34203624]
[60]
Purkait A, Mukherjee A, Hazra DK, Roy K, Biswas PK, Kole RK. Encapsulation, release and insecticidal activity of Pongamia pinnata (L.) seed oil. Heliyon 2021; 7(3): e06557.
[http://dx.doi.org/10.1016/j.heliyon.2021.e06557] [PMID: 33855235]
[61]
Shailajan S, Menon S, Pednekar S, Singh A. Wound healing efficacy of Jatyadi Taila: In vivo evaluation in rat using excision wound model. J Ethnopharmacol 2011; 138(1): 99-104.
[http://dx.doi.org/10.1016/j.jep.2011.08.050] [PMID: 21907784]

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