Abstract
Mucuna pruriens Linn. (M. pruriens), a leguminous plant, was used extensively in Ayurveda, to treat male-related infertility. Previous studies have demonstrated antioxidant, androgenic, aphrodisiac, and spermatogenic properties of M. pruriens seed extract. Surprisingly, the biological activities of M. pruriens on aging-induced pathological changes in the testis microenvironment have never been explored and the present study was focused on the testing therapeutic efficacy of M. pruriens on aged rat testis. Male Wistar albino rats were grouped as; adult (3 months), aged (24 months), aged + M. pruriens and adult + M. pruriens (N = 6/group). The extract was administrated at a dose of 200 mg/kg body weight (dosage determined in our previous study) daily by gavage for 60 days. The total and free testosterone, FSH and LH levels were considerably increased in aged + M. pruriens. The diameter & volume of the seminiferous tubules, the height & volume of the epithelium, and the number of Leydig cells number were significantly decreased in aged rat testis, concomitantly connective tissue proportion was increased compared to adult rats. The seminiferous epithelium indicates significant rejuvenation or restoration of spermatogenic cells in aged + M. pruriens rat testis. The highlighting observations in aged + M. pruriens was increased in the following parameters i.e., tubular diameter (25%), number of tubules (35%), epithelial height (25%) & volume (20%), and number of Leydig cells (35%) when compared to untreated aged rat testis. The TNFα, NF-κB, cytochrome c, Caspase-9, Caspase-3, Bcl-2, Bax, PARP iNOS, and inflammatory and apoptotic factors were downregulated in aged + M. pruriens. M. pruriens was able to restore spermatogenesis and enhance the activity of Sertoli cells and Leydig cells and improve the pituitary–gonadal axis in aged rat testis and observations indicate the therapeutic activity of M. pruriens in aged rat testis.
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References
Abrishamdar M, Jalali MS, Farbood Y (2022) Targeting mitochondria as a therapeutic approach for Parkinson’s disease. Cell Mol Neurobiol. https://doi.org/10.1007/s10571-022-01265-w
Adebowale YA, Adeyemi A, Oshodi AA (2005) Variability in the physicochemical, nutritional and antinutritional attributes of six Mucuna species. Food Chem 89:37–48
Avoseh ON, Ogunwande IA, Ojenike GO, Mtunzi FM (2020) Volatile composition, toxicity, analgesic, and anti-inflammatory activities of Mucuna pruriens. Published Online. https://doi.org/10.1177/1934578X20932326
Beattie MC, Adekola L, Papadopoulos V, Chen H, Zirkin BR (2015) Leydig cell aging and hypogonadism. Exp Gerontol 68:87–91. https://doi.org/10.1016/j.exger.2015.02.014
Beutler E, Duron O, Kelly BM (1963) Improved method for the determination of blood glutathione. J Lab Clin Med 61:882–888
Bhanmeechao C, Srisuwatanasagul S, Ponglowhapan S (2018) Age-related changes in interstitial fibrosis and germ cell degeneration of the canine testis. Reprod Domest Anim 53(Suppl 3):37–43. https://doi.org/10.1111/rda.13354
Bivalacqua TJ, Musicki B, Hsu LL, Berkowitz DE, Champion HC, Burnett AL (2013) Sildenafil citrate-restored eNOS and PDE5 regulation in sickle cell mouse penis prevents priapism via control of oxidative/nitrosative stress. PLoS One 8:e68028. https://doi.org/10.1371/journal.pone.0068028
Bonfoco E, Krainc D, Ankarcrona M, Nicotera P, Lipton SA (1995) Apoptosis and necrosis: two distinct events induced, respectively, by mild and intense insults with N-methyl-D-aspartate or nitric oxide/superoxide in cortical cell cultures. Proc Natl Acad Sc USA 92:7162–7166
Chen H, Mruk DD, Lee WM, Cheng CY (2017) Regulation of spermatogenesis by a local functional axis in the testis: role of the basement membrane-derived noncollagenous 1 domain peptide. FASEB J 31(8):3587–3607. https://doi.org/10.1096/fj.201700052R
Coştur P, Filiz S, Gonca S et al (2012) Êxpression of inducible nitric oxide synthase (iNOS) in the azoospermic human testis. Andrologia 44(Suppl 1):654–660. https://doi.org/10.1111/j.1439-0272.2011.01245.x
Cudicini C, Lejeune H, Gomez E, Bosmans E, Ballet F, Saez J, Jegou B (1997) Human Leydig cells and Sertoli cells are producers of interleukins-1 and-6. J Clinical Endocrinol Metabol 82:1426–1433
D’Cruz SC, Vaithinathan S, Jubendradass R, Mathur PP (2010) Effects of plants and plant products on the testis. Asian J Androl 12(4):468–479. https://doi.org/10.1038/aja.2010.43
Desai ID (1984) Vitamin E analysis methods for animal tissues. Methods Enzymol 105:138–147. https://doi.org/10.1016/s0076-6879(84)05019-9
Dhale D, Sanskruti P (2010) Pharmacognostic evaluation of Mucuna pruriens (L) Dc. (Fabaceae). Int J Pharma World Res 1:1–13
Dominguez JM, Davis RT, McCullough DJ, Stabley JN, Behnke BJ (2011) Aging and exercise training reduce testes microvascular PO2 and alter vasoconstrictor responsiveness in testicular arterioles. Am J Physiol Regul Integr Comp Physiol 301(3):R801–R810. https://doi.org/10.1152/ajpregu.00203.2011
Ekor M (2013) The growing use of herbal medicines: issues relating to adverse reactions and challenges in monitoring safety. Front Pharmacol 2013(4):177. https://doi.org/10.3389/fphar.2013.00177
Elias H, Hyde DM (1980) An elementary introduction to stereology (quantitative microscopy). Am J Anat 159(4):412–446. https://doi.org/10.1002/aja.1001590407
Ellman GL (1959) Tissue sulfhydryl groups groups. Arch Biochem Biophys 72:70–77
Fabian D, Flatt T (2011) The evolution of aging. Nat Educ Knowl 3:9
Fang YZ, Yang S, Wu G (2002) Free radicals, antioxidants, and nutrition. Nutrition 18:872–879. https://doi.org/10.1016/s0899-9007%2802%2900916-4
Flatt T (2012) A new definition of aging? Front Genet 3:148
Frungieri MB, Calandra RS, Bartke A, Matzkin ME (2021) Male and female gonadal ageing: Its impact on health span and life span. Mech Ageing Dev 197:111519. https://doi.org/10.1016/j.mad.2021.111519
Fujisawa M, Tatsumi N, Fujioka H, Kanzaki M, Okuda Y, Arakawa S (2000) Nitric oxide production of rat Leydig and Sertoli cells is stimulated by round spermatic factors. Mol Cell Endocrinol 160: 99–105
Galluzzi L, Vitale I, Aaronson S et al (2018) Molecular mechanisms of cell death: recommendations of the Nomenclature Committee on Cell Death 2018. Cell Death Differ 25:486–541. https://doi.org/10.1038/s41418-017-0012-4
Gunes S, Hekim GN, Arslan MA, Asci R (2016) Effects of aging on the male reproductive system. J Assist Reprod Genet 33(4):441–454. https://doi.org/10.1007/s10815-016-0663-y
Habig WH, Pabst MJ, Jakoby WB, Jakoby WB (1974) Glutathione S-Transferases the first enzymatic step in mercapturic acid formation. J Biol Chem 249:7130–7139
Harborne JB (1973) Phytochemical Methods. Chapman and Hall Ltd., London, 49–188
Hedger M (2011) Immunophysiology and pathology of inflammation in the testis and epididymis. J Androl 32:625–640. https://doi.org/10.2164/jandrol.111.012989
Heimlich G, McKinnon AD, Bernardo K et al (2004) Bax-induced cytochrome c release from mitochondria depends on alpha-helices-5 and -6. Biochem J 378:247–255. https://doi.org/10.1042/BJ20031152
Hikim AP, Amador AG, Klemcke HG, Bartke A, Russell LD (1989) Correlative morphology and endocrinology of Sertoli cells in hamster testes in active and inactive states of spermatogenesis. Endocrinology 125(4):1829–1843
Huang D, Wei W, Xie F, Zhu X, Zheng L, Lv Z (2018) Steroidogenesis decline accompanied with reduced antioxidation and endoplasmic reticulum stress in mice testes during ageing. Andrologia 50:e12816. https://doi.org/10.1111/and.12816
Itoh M, Xie Q, Miyamoto K, Takeuchi Y (1999) Major differences between the testis and epididymis in the induction of granulomas in response to extravasated germ cells. I. A light microscopical study in mice. Int J Androl 22(5):316–323. https://doi.org/10.1046/j.1365-2605.1999.00186.x
Javier R, Francisco M-G, Pilar G-P, Alvaro S, Manuel N, Carlos S-Q (2001) Androgen receptor expression in sertoli cells as a function of seminiferous tubule maturation in the human cryptorchid testis. J Clinic Endocrinol Metabol 86(1):413–421. https://doi.org/10.1210/jcem.86.1.7109
Johnson KJ (2015) Testicular histopathology associated with disruption of the Sertoli cell cytoskeleton. Spermatogenesis 4(2):e979106. https://doi.org/10.4161/21565562.2014.979106
Kalwar Q, Chu M, Ahmad AA, Ding X, Wu X, Bao P, Yan P (2019) Morphometric evaluation of spermatogenic cells and seminiferous tubules and exploration of luteinizing hormone beta polypeptide in testis of Datong Yak. Animals (basel) 10(1):66. https://doi.org/10.3390/ani10010066
Kanazawa K, Sakakibara H (2000) High content of dopamine, a strong antioxidant Cavendish banana. J Agric Food Chem 48(3):844–848. https://doi.org/10.1021/jf9909860. (PMID: 10725161)
Khandelwal N, Simpson J, Taylor G et al (2011) Nucleolar NF-κB/RelA mediates apoptosis by causing cytoplasmic relocalization of nucleophosmin. Cell Death Differ 18:1889–1903. https://doi.org/10.1038/cdd.2011.79
Klonoff-Cohen HS, Natarajan L (2004) The effect of advancing paternal age on pregnancy and live birth rates in couples undergoing in vitro fertilization or gamete intrafallopian transfer. Am J Obstet Gynecol 191(2):507–514
Lampariello LR, Cortelazzo A, Guerranti R, Sticozzi C, Valacchi G (2012) The magic velvet bean of Mucuna pruriens. J Tradit Complement Med 2(4):331–339. https://doi.org/10.1016/s2225-4110(16)30119-5
Liguori I, Russo G, Curcio F et al (2018) Oxidative stress, aging, and diseases. Clin Interv Aging 13:757–772. https://doi.org/10.2147/CIA.S158513
Liu G, Gong P, Zhao H, Wang Z, Gong S, Cai L (2006) Effect of low-level radiation on the death of male germ cells. Radiat Res 165:379–389. https://doi.org/10.1667/rr3528.1
Machado KN, Paula Barbosa A, de Freitas AA, Alvarenga LF, Pádua RM, Gomes Faraco AA, Braga FC, Vianna-Soares CD, Castilho RO (2021) TNF-α inhibition, antioxidant effects and chemical analysis of extracts and fraction from Brazilian guaraná seed powder. Food Chem 355:129563. https://doi.org/10.1016/j.foodchem.2021.129563
Marklund S, Marklund G (1974) Involvement of the superoxide anion radical in the autoxidation of pyrogallol and a convenient assay for superoxide dismutase. Eur J Biochem 47:469–474
Marouani N, Hallegue D, Sakly M, Benkhalifa M, Ben Rhouma K, Tebourbi O (2017) p, p′-DDT induces testicular oxidative stress-induced apoptosis in adult rats. Reprod Biol Endocrinol 15(1):40. https://doi.org/10.1186/s12958-017-0259-0
Matzkin ME, Miquet JG, Fang Y et al (2016) Alterations in oxidative, inflammatory and apoptotic events in short-lived and long-lived mice testes. Aging (albany NY) 8(1):95–110. https://doi.org/10.18632/aging.100875
Matzkin ME, Valchi P, Riviere E, Rossi SP, Tavalieri YE, Muñoz de Toro MM, Mayerhofer A, Bartke A, Calandra RS, Frungieri MB (2019) Aging in the Syrian hamster testis: Inflammatory-oxidative status and the impact of photoperiod. Exp Gerontol 124:110649. https://doi.org/10.1016/j.exger.2019.110649
Matzkin ME, Calandra RS, Rossi SP, Bartke A, Frungieri MB (2021) Hallmarks of testicular aging: the challenge of anti-inflammatory and antioxidant therapies using natural and/or pharmacological compounds to improve the physiopathological status of the aged male gonad. Cells 10:3114. https://doi.org/10.3390/cells10113114
Misra L, Wagner H (2004) Alkaloidal constituents of Mucuna pruriens seeds. Phytochemistry 65:2565–2567
Mize CE, Langdon RG (1962) Hepatic glutathione reductase. I. Purification and general kinetic properties. J Biol Chem 237:1589–1595
Mohamad NV, Wong SK, Wan-Hasan WN, Jolly JJ, Nur-Farhana MF, Ima-Nirwana S, Chin KY (2019) The relationship between circulating testosterone and inflammatory cytokines in men. Aging Male 22(2):129–140. https://doi.org/10.1080/13685538.2018.1482487
Mundy WR, Freudenrich TM, Kodavanti PRS (1997) Aluminum potentiates glutamate-induced calcium accumulation and iron-induced oxygen free radical formation in primary neuronal cultures. Mol Chem Neuropathol 32: 41–57. https://doi.org/10.1007/BF02815166
Mularoni V, Esposito V, Di Persio S, Vicini E, Spadetta G, Berloco P, Fanelli F, Mezzullo M, Pagotto U, Pelusi C et al (2020) Age-related changes in human Leydig cell status. Hum Reprod 35:2663–2676. https://doi.org/10.1093/humrep/deaa271
Murugesan A, Ganesh Mohanraj K, Wungpam Shimray K, Iqbal Khan MZ, Prakash S (2022) Therapeutic potential of Mucuna pruriens (Linn.) on high-fat diet-induced testicular and sperm damage in rats. Avicenna J Phytomed. 12(5):489–502. https://doi.org/10.22038/AJP.2022.20261
Nguyen-Powanda P, Robaire B (2020) Oxidative stress and reproductive function in the aging male. Biology (basel). 9(9):282. https://doi.org/10.3390/biology9090282
Ohkawa H, Ohishi N, Yagi K (1979) Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem 95:351–358
Omaye ST, Turnbull JD, Sauberlich HE (1979) Selected methods for the determination of ascorbic acid in animal cells, tissues, and fluids. Methods Enzymol 62:3–11. https://doi.org/10.1016/0076-6879(79)62181-x
Pandey G (1998) Chamatkari Jadi-Butiyan. Bhasha Bhavan, Mathura, India
Pandey U (1999) Chamatkari paudhe. Bhagwati Pocket Books, Agra
Pant MC, Joshi LD (1970) Identification of pharmacologically active substances in seed of Mucuna pruriens DC. Indian J Pharmacol 2:24
Paoli D, Pecora G, Pallotti F, Faja F, Pelloni M, Lenzi A et al (2019) Cytological and molecular aspects of the ageing sperm. Hum Reprod 34(2):218–227. https://doi.org/10.1093/humrep/dey357
Pataky MW, Young WF, Nair KS (2021) Hormonal and metabolic changes of aging and the influence of lifestyle modifications. Mayo Clin Proc 96:788–814
Pathania R, Chawla P, Khan H et al (2020) An assessment of potential nutritive and medicinal properties of Mucuna pruriens: a natural food legume. 3 Biotech 10:261. https://doi.org/10.1007/s13205-020-02253-x
Phaniendra A, Jestadi DB, Periyasamy L (2015) Free radicals: properties, sources, targets, and their implication in various diseases. Indian J Clin Biochem 30(1):11–26. https://doi.org/10.1007/s12291-014-0446-0
Pick E, Keisari Y (1981) Superoxide anion and hydrogen peroxide production by chemically elicited peritoneal macrophages induced by multiple non-phagocytic stimuli. Cellular Immunol 59: 301–318
Podczasy JJ, Wei R (1988) Reduction of iodonitrotetrazolium violet by superoxide radicals. Biochem Biophys Res Commun 150:1294–1301
Prakash D, Niranjan A, Tewari SK (2001) Some nutritional properties of the seeds of three Mucuna species. Int J Food Sci Nutr 52(1):79–82
Prakash S, Kamakshi K (2014) Long-term study of vasectomy in Macaca radiata--histological and ultrasonographic analysis of testis and duct system. Syst Biol Reprod Med 60:151–160. https://doi.org/10.3109/19396368.2014.896957
Prakash S, Prithiviraj E, Suresh S (2008) Developmental changes of seminiferous tubule in prenatal, postnatal and adult testis of bonnet monkey (Macaca radiata). Anat Histol Embryol 37(1):19–23. https://doi.org/10.1111/j.1439-0264.2007.00789.x
Prakash S, Muhammed I, Mohanraj KG, Premavathy D, Muthu SJ, Wungpam K et al (2018) Therapeutic potential of Mucuna pruriens (Linn) on ageing induced damage in the dorsal nerve of the penis and its implication on erectile function: an experimental study using albino rats. Aging Male. https://doi.org/10.1080/13685538.2018.1439005
Prakash S, Muhammed I, Mohammad ZIK, Sathyanathan SB (2020) Pathobiology of ischiocavernosus and bulbospongiosus muscles in long-term diabetic male rats and its implication on erectile dysfunction. Aging Male 23(5):979–990. https://doi.org/10.1080/13685538.2019.1647160
Puntarulo S, Cederbaum AI (1988) Production of reactive oxygen species by microsomes enriched in specific human cytochrome P450 enzymes. Free Radic Biol Med 24:1324–1330
Rachsee A, Chiranthanut N, Kunnaja P et al (2021) Mucuna pruriens (L) DC seed extract inhibits lipopolysaccharide-induced inflammatory responses in BV2 microglial cells. J Ethnopharmacol 267:113518. https://doi.org/10.1016/j.jep.2020.113518
Reuben-Kalu J, Renuka R, Uma D, Gnanam R, SanthanakrishnanV P, Alum EA (2021) Phytochemical and in-silico evaluation of the pharmaceutically important biomolecules present in leaf and seed extracts of Mucuna pruriens. Madras Agric J 107:10–12. https://doi.org/10.29321/MAJ.10.000566/
Rima, Ishmayana S, Malini DM, Soedjanaatmadja UMS (2023) Nutritional content and the activities of l-Dopa (L-3,4-dihydoxyphenyalanine) from Mucuna pruriens L DC seeds of Central Java accession. Arab J Chem 16:1. https://doi.org/10.1016/j.arabjc.2022.104390
Rotruck JT, Pope AL, Ganther HE, Swanson AB, Hafeman DG, Hoekstra WG (1973) Selenium: biochemical role as acomponent of glutathione peroxidase. Science 179:588–590
Roustaei Z, Raisanen S, Gissler M, Heinonen S (2019) Fertility rates and the postponement of first births: a descriptive study with Finnish population data. BMJ Open 9(1):e026336. https://doi.org/10.1136/bmjopen-2018-026336
Santiago J, Silva JV, Alves MG, Oliveira PF, Fardilha M (2019) Testicular aging: an overview of ultrastructural, cellular, and molecular alterations. J Gerontol A Biol Sci Med Sci 74:860–871. https://doi.org/10.1093/gerona/gly082
Sathiyanarayanan L, Arulmozhi S (2007) Mucuna pruriens Linn.—a comprehensive review. Pharmacogn Rev 1:157–162
Sengupta P (2013) The laboratory rat: relating its age with human’s. Int J Prev Med 4:624–630
Shukla KK, Mahdi AA, Ahmad MK, Shankhwar SN, Rajender S, Jaiswar SP (2009) Mucuna pruriens improves male fertility by its action on the hypothalamus-pituitary-gonadal axis. Fertil Steril 92(6):1934–1940. https://doi.org/10.1016/j.fertnstert.2008.09.045. (Epub 2008 Oct 29 PMID: 18973898)
Singh AP, Sarkar S, Tripathi M, Rajender S (2013) Mucuna pruriens and its major constituent L-DOPA recover spermatogenic loss by combating ROS, loss of mitochondrial membrane potential and apoptosis. PLoS ONE 8(1):e54655. https://doi.org/10.1371/journal.pone.0054655
Singh SK, Dhawan SS, Lal RK, Shanker K, Singh M (2018) Biochemical characterization and spatio-temporal analysis of the putative L-DOPA pathway in Mucuna pruriens. Planta 248(5):1277–1287. https://doi.org/10.1007/s00425-018-2978-7
Sinha AK (1972) Colorimetric assay of catalase. Anal Biochem 47:389–394
Siu MK, Lee WM, Cheng CY (2003) The interplay of collagen IV, tumor necrosis factor-alpha, gelatinase B (matrix metalloprotease-9), and tissue inhibitor of metalloproteases-1 in the basal lamina regulates Sertoli cell-tight junction dynamics in the rat testis. Endocrinology 144(1):371–387. https://doi.org/10.1210/en.2002-220786
Stucker S, De Angelis J, Kusumbe AP (2021) Heterogeneity and dynamics of vasculature in the endocrine system during aging and disease. Front Physiol 12:624928. https://doi.org/10.3389/fphys.2021.624928
Suresh S, Prakash S (2011) Effect of Mucuna pruriens (Linn.) on oxidative stress-induced structural alteration of corpus cavernosum in streptozotocin-induced diabetic rat. J Sex Med 8:1943–1956. https://doi.org/10.1111/j.1743-6109.2011.02221.x
Suresh S, Prakash S (2012) Effect of Mucuna pruriens (Linn.) on sexual behavior and sperm parameters in streptozotocin-induced diabetic male rat. J Sex Med 9:3066–3078. https://doi.org/10.1111/j.1743-6109.2010.01831.x
Suresh S, Prithiviraj E, Prakash S (2009) Dose-and time-dependent effects of ethanolic extract of Mucuna prureins Linn. seed on sexual behaviour of normal male rats. Dose-and time-dependent effects of ethanolic extract of Mucuna pruriens Linn. seed on sexual behaviour of normal male rats. J Ethnopharmacol 122:497–501. https://doi.org/10.1016/j.jep.2009.01.032
Suresh S, Prithiviraj E, Prakash S (2010) Effect of Mucuna pruriens on oxidative stress mediated damage in aged rat sperm. Int J Androl 33:22–32
Suresh S, Prithiviraj E, Venkatalakshmi N, Ganesh MK, Ganesh L, Lee HJ, Prakash S (2011) Spermatogenic and Antioxidant Potential of Mucuna prureins (L.) in Epididymal Spermatozoa: A Dose Dependent Effect. Reprod Develop Biol 35:441–447
Suresh S, Prithiviraj E, Venkata-Lakshmi N, Karthik-Ganesh M, Ganesh L, Prakash S (2013) Effect of Mucuna pruriens (Linn.) on mitochondrial dysfunction and DNA damage in epididymal sperm of streptozotocin induced diabetic rat. J Ethnopharmacol 145:32–41
Swain SR, Sinha BN, Murthy PN (2008) Anti-inflammatory, diuretic and antimicrobial activities of Rungia pectinata Linn and Rungia repens Nees. Indian J Pharm Sci 70(5):679–683. https://doi.org/10.4103/0250-474X.45418
Theas MS (2018) Germ cell apoptosis and survival in testicular inflammation. Andrologia 50(11):e13083. https://doi.org/10.1111/and.13083
Vaiserman AM, Lushchak OV (2017) Anti-aging drugs: where are we and where are we going? In: Anti-aging drugs: from basic research to clinical practice. pp. 1–10 https://doi.org/10.1039/9781782626602-00001
Weinstein DM, Mihm MJ, Bauer JA (2000) Cardiac peroxynitrite formation and left ventricular dysfunction following doxorubicin treatment in mice. J Pharmacol Exp Ther 294: 396–401
Xiong S, Mu T, Wang G et al (2014) Mitochondria-mediated apoptosis in mammals. Protein Cell 5:737–749. https://doi.org/10.1007/s13238-014-0089-1
Yang WR, Li BB, Hu Y, Zhang L, Wang XZ (2020) Oxidative stress mediates heat-induced changes of tight junction proteins in porcine Sertoli cells via inhibiting CaMKKβ-AMPK pathway. Theriogenology 142:104–113. https://doi.org/10.1016/j.theriogenology.2019.09.031
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PS: Conceived the study idea, methodology design, acquiring funding for the research, consolidating data, and writing the manuscript. KGM: Performed the experimental, data collection and statistical analysis. GL: Performed the experiment and consolidated data. MZIK: Performed the experiment and consolidated data. All authors participated in interpreting the results, reviewing drafts of the manuscript, and approving the final version of the manuscript submitted for publication. In addition, all authors read and approved the final manuscript.
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The study was approved by the Institutional Animal Ethical Committee (IAEC), Dr. ALMPGIBMS, University of Madras (IAEC Approval No. 04/02/2011). The quarantine procedures and animal maintenance were according to the recommendations of the Committee for the Purpose of Control and Supervision of Experiments on Animals (CPCSEA), India, and guidelines for laboratory animal facility in India. The manuscript does not contain data from any person. Data presented were from animal studies (approved by the Institutional Animal Ethical Committee (IAEC), Dr. ALM PGIBMS, University of Madras, Taramani—details given above) All the authors have given their consent for publishing.
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Ganesh, M.K., Lakshmanan, G., Khan, M.Z.I. et al. Aging induced testicular damage: analyzing the ameliorative potential of Mucuna pruriens seed extract. 3 Biotech 13, 206 (2023). https://doi.org/10.1007/s13205-023-03618-8
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DOI: https://doi.org/10.1007/s13205-023-03618-8