Abstract
Infertility is a significant cause of anxiety, depression, and social stigma among couples and families. In such cases, male reproductive factors contribute widely to the extent of 20–70%. Male infertility is a multifactorial disease with several complications contributing to its diagnosis. Although its management encompasses both modern and traditional medicine arenas, the first line of treatment, adopted by most males, focuses on the reasonably successful medicinal plant-based conventional therapies. Phyto-therapeutics, which relies on active ingredients from traditionally known herbs, influences sexual behavior and male fertility factors. The potency of these phyto-actives depends on their preparation methods and forms of consumption, including decoctions, extracts, semi-purified compounds, etc., as inferred from in vitro and in vivo (laboratory animal models and human) studies. The mechanisms of action therein involve the testosterone pathway for stimulation of spermatogenesis, reduction of oxidative stress, inhibition of inflammation, activation of signaling pathways in the testes [extracellular-regulated kinase (ERK)/protein kinase B(PKB)/transformation of growth factor-beta 1(TGF-β1)/nuclear factor kappa-light-chain-enhancer of activated B cells NF-kB signaling pathways] and mediation of sexual behavior. This review critically focuses on the medicinal plants and their potent actives, along with the biochemical and molecular mechanisms that modulate vital pathways associated with the successful management of male infertility. Such intrinsic knowledge will significantly further studies on medicinal plants that improve male reproductive health.
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Change history
18 April 2022
A Correction to this paper has been published: https://doi.org/10.1007/s11418-022-01625-2
References
Kashani HH, Faraji Z, Nikzad H, Parivar K, Nikzad M (2012) The effect of aqueous extract of Salep prepared from root-tubers of Dactylorhiza maculate (Orchidaceae) on the testes and sexual hormones of immature male mice. J Med Plant Res 6:4102–4106
Henkel R, Maaß G, Bödeker RH, Scheibelhut C, Stalf T, Mehnert C, Schuppe HC, Jung A, Schill WB (2005) Sperm function and assisted reproduction technology. Reprod Med Biol 4:7–30
Toshimori K, Ito C, Maekawa M, Toyama Y, Suzuki-Toyota F, Saxena DK (2004) Impairment of spermatogenesis leading to infertility. Anat Sci Int 79:101–111
Bhagwati S, Singh R (2017) Plant products in the management of male infertility. In: Male infertility: understanding, causes and treatment. Springer, p 381–399
Jaradat N, Zaid AN (2019) Herbal remedies used for the treatment of infertility in males and females by traditional healers in the rural areas of the West Bank/Palestine. BMC Complement Altern Med 19:1–2
Rates SM (2001) Plants as source of drugs. Toxicon 39:603–613
Austin DF (1991) Ipomoea littoralis (Convolvulaceae)—taxonomy, distribution, and ethnobotany. Econ Bot 45:251–256
Zhang X (2002) World Health Organization. Traditional medicine strategy 2002–2005
Carpentier M, Sahpaz S, Bailleul F (2004) Plantes et dysfonction érectile. Phytothérapie 2:66–71
Noumi E, Zollo A, Lontsi D (1998) Aphrodisiac plants used in Cameroon. Fitoterapia (Milano) 69:125–134
Low WY, Tan HM (2007) Asian traditional medicine for erectile dysfunction. J Mens Health Gend 4:245–250
Chauhan NS, Sharma V, Dixit VK, Thakur M (2014) A review on plants used for improvement of sexual performance and virility. Biomed Res Int. https://doi.org/10.1155/2014/868062
Singh G, Mukherjee T (1998) Herbal aphrodisiacs: a review. Indian Drugs 35:175–182
Rakuambo NC, Meyer JJ, Hussein A, Huyser C, Mdlalose SP, Raidani TG (2006) In vitro effect of medicinal plants used to treat erectile dysfunction on smooth muscle relaxation and human sperm. J Ethnopharmacol 105:84–88
Abarikwu SO, Onuah CL, Singh SK (2020) Plants in the management of male infertility. Andrologia 52:e13509
Agbodjento E (2021) Ethnobotanical knowledge of medicinal plants used in the treatment of male infertility in southern Benin. Adv Trad Med 21:655–673
Yu A, Zhang F, Zhang F (2004) Clinical observation on effect of combination of zhuanyindan and hormone in treating male infertility with positive antisperm antibody. Zhongguo Zhong Xi Yi Jie He Za Zhi 24:223–226
Yue G, Chen Q, Dai N (1997) Experimental study on effect of bushen shengjing decoction on kidney yang and testicular dysfunction in rats. Zhongguo Zhong Xi Yi Jie He Za Zhi 17:289–291
Ma J, Wang ZR, Lu ZF (2006) Regulatory effect of Wenyang Whengling Decoction on Smads expressions in testis of sterile rats with Shen-yang deficiency. Zhongguo Zhong Xi Yi Jie He Za Zhi 26:1107–1113
Jiang D (2017) Effect of Chinese herbal medicine on male infertility. Int Rev Neurobiol 135:297–311
Wang J, Wang Q, Liu BX, Li DH, Zhang HM, Yuan ZJ (2012) Shugan Yiyang capsule increases the expressions of VEGF, IGF and Akt1 in the rat model of arteriogenic erectile dysfunction. Zhonghua Nan Ke Xue 18:184–188
Zhang H, Zhao H, Zhang A (2007) Male infertility with severe oligospermatism and azoospermia treated by Bushen Shengjing Decoction combined with intracytoplasmic sperm injection. Zhongguo Zhong Xi Yi Jie He Za Zhi 27:972–975
Wang JH, Chen D, Zhou JG, Cao YG, Jia JM (2008) Construction of the male rat model of adenine-induced infertility with kidney-yang deficiency. Zhonghua Nan Ke Xue 14:565–570
Wang ZQ, Huang YQ, Liang B (2008) Clinical observation on electroacupuncture and Chinese drug for treatment of oligospermia and asthenospermia of the male infertility patient. Zhongguo Zhen Jiu 28:805–807
Liao ZJ, Zhou JF, Yin ZC, Zhang JJ, Xiang ST, Wang SS, Chen ZQ (2013) Short-course kidney-invigorating therapy improves near-term semen quality in asthenozoospermic men with kidney deficiency. Zhonghua Nan Ke Xue 19:159–162
Zeng JX, Dai XH, Liu JH, Yang JH, Chen JF, Lin MN (2003) Effects of shouwu-huanjing recipe on human sperm motility and fertility in vitro. Zhonghua Nan Ke Xue 9:476–479
Han Q, Liu DC, Wang F, Guo J (2015) Treatment of asthenozoospermia men with shen-essence deficiency syndrome by Yishen Zhongzi Pill: a clinical study. Zhongguo Zhong Xi Yi Jie He Za Zhi 35:1050–1053
Roozbeh N, Amirian A, Abdi F, Haghdoost SA (2021) A systematic review on use of medicinal plants for male infertility treatment. J Family Reprod Health 15:74–81
Yakubu MT, Akanji MA, Oladiji AT, Adesokan AA (2008) Androgenic potentials of aqueous extract of Massularia acuminata (G. Don) Bullock ex Hoyl. stem in male Wistar rats. J Ethnopharmacol 118:508–513
Consensus NI (1993) Development panel on impotence. NIH consensus conference. Impotence. JAMA 270:83–90
Ogah G (1999) Impotence. Nig J Gen Pract 3:30–41
Bhatwadekar AD, Chintawar SD, Logade NA, Somani RS, Veena KS, Kasture SB (1999) Antistress activity of Butea monosperma flowers. Indian J Pharmacol 31:153
Rane A, Gramurohit ND (1998) Hepatoprotective activity of Ptreocarpus marsupium Roxb. and Butea frondosa Koen. ex. Roxb. Indian J Pharm Sci 60:182
Shah KG, Baxi AJ (1990) Phytochemical studies and antioestrogenic activity of Butea frondosa flowers. Indian J Pharm Sci 52:272
Mengi SA, Deshpande SG (1995) Comparative evaluation of Butea frondosa and flurbiprofen for ocular anti-inflammatory activity in rabbits. J Pharm Pharmacol 47:997–1001
Ramachandran S, Sridhar Y, Sam SK, Saravanan M, Leonard JT, Anbalagan N, Sridhar SK (2004) Aphrodisiac activity of Butea frondosa Koen. ex Roxb. extract in male rats. Phytomedicine 11:165–168
Ratnasooriya WD, Dharmasiri MG (2000) Effects of Terminalia catappa seeds on sexual behaviour and fertility of male rats. Asian J Androl 2:213–220
Abdulwaheb M, Makonnen E, Debella A, Abebe D (2007) Effect of Catha edulis foresk (khat) extracts on male rat sexual behavior. J Ethnopharmacol 110:250–256
Kalix P (1992) Cathinone, a natural amphetamine. Pharmacol Toxicol 70:77–86
Ahmad S, Latif A, Qasmi IA (2004) Effect of 50% ethanolic extract of Syzygium aromaticum (L.) Merr. & Perry. (clove) on sexual behaviour of normal male rats. BMC Complement Altern Med 4:1–7
Kumar PS, Subramoniam A, Pushpangadan P (2000) Aphrodisiac activity of Vanda tessellata (Roxb.) Hook. ex Don extract in male mice. Indian J Pharmacol 32:300–304
Ahmad S, Latif A, Qasmi IA, Amin KM (2005) An experimental study of sexual function improving effect of Myristica fragrans Houtt. (nutmeg). BMC Complement Altern Med 5:1–7
Gallegos AJ (1985) The zoapatle VI. Revisited. Contraception 31:487–497
Perusquía M, Sánchez E, Ponce-Monter H, Estrada AV, Pedrón N, Valencia A, Guzmán A, Gallegos AJ (1985) The Zoapatle XI. Effects elicited by Mmontanoatomentosa and Montanoafrutescens on rat uterine strips. Contraception 31:543–551
Gimpl G, Fahrenholz F (2001) The oxytocin receptor system: structure, function, and regulation. Physiol Rev 81:629–683
Carro-Juárez M, Cervantes E, Cervantes-Méndez M, Rodrıguez-Manzo G (2004) Aphrodisiac properties of Montanoa tomentosa aqueous crude extract in male rats. Pharmacol Biochem Behav 78:129–134
Thakur M, Dixit VK (2007) Aphrodisiac activity of Dactylorhiza hatagirea (D. Don) Soo in male albino rats. Evid Based Complementary Altern Med 4:29–31
Makarova MN, Pozharitskaya ON, Shikov AN, Tesakova SV, Makarov VG, Tikhonov VP (2007) Effect of lipid-based suspension of Epimedium koreanum Nakai extract on sexual behavior in rats. J Ethnopharmacol 114:412–416
Ning H, Xin ZC, Lin G, Banie L, Lue TF, Lin CS (2006) Effects of icariin on phosphodiesterase-5 activity in vitro and cyclic guanosine monophosphate level in cavernous smooth muscle cells. Urology 68:1350–1354
Yakubu MT, Akanji MA, Oladiji AT (2005) Aphrodisiac potentials of the aqueous extract of Fadogia agrestis (Schweinf. Ex Hiern) stem in male albino rats. Asian J Androl 7:399–404
Shah GR, Chaudhari MV, Patankar SB, Pensalwar SV, Sabale VP, Sonawane NA (2012) Evaluation of a multi-herb supplement for erectile dysfunction: a randomized double-blind, placebo-controlled study. BMC Complement Altern Med 12:1–9
De Andrade E, De Mesquita AA, de Almeida CJ, De Andrade PM, Ortiz V, Paranhos M, Srougi M, Erdogrun T (2007) Study of the efficacy of Korean Red Ginseng in the treatment of erectile dysfunction. Asian J Androl 9:241–244
Tachikawa E, Kudo K, Harada K, Kashimoto T, Miyate Y, Kakizaki A, Takahashi E (1999) Effects of ginseng saponins on responses induced by various receptor stimuli. Eur J PharmacSol 369:23–32
O’Hara M, Kiefer D, Farrell K, Kemper K (1998) A review of 12 commonly used medicinal herbs. Arch Fam Med 7:523
Kimura T, Saunders PA, Kim HS, Rheu HM, Oh KW, Ho IK (1994) Interactions of ginsenosides with ligand-bindings of GABA (A) and GABA (B) receptors. Gen Pharmacol 25:193–199
Gonzales GF, Córdova A, Vega K, Chung A, Villena A, Góñez C, Castillo S (2002) Effect of Lepidium meyenii (MACA) on sexual desire and its absent relationship with serum testosterone levels in adult healthy men. Food Chem Toxicol 34:367–372
Kuiper GG, Lemmen JG, Carlsson BO, Corton JC, Safe SH, Van Der Saag PT, Van Der Burg B, Gustafsson JA (1998) Interaction of estrogenic chemicals and phytoestrogens with estrogen receptor β. Endocrinology 139:4252–4263
Rochira V, Balestrieri A, Madeo B, Baraldi E, Faustini-Fustini M, Granata AR, Carani C (2001) Congenital estrogen deficiency: in search of the estrogen role in human male reproduction. Mol CellS Endocrinol 178:107–115
O’donnell L, Robertson KM, Jones ME, Simpson ER (2001) Estrogen and spermatogenesis. Endocr Rev 22:289–318
Paccola CC, Miraglia SM (2015) Prenatal and lactation nicotine exposure affects Sertoli cell and gonadotropin levels in rats. Reproduction (Cambridge, England) 151:117–133
Aydos K, Güven MC, Can B, Ergün A (2001) Nicotine toxicity to the ultrastructure of the testis in rats. BJU Int 88:622–626
Oyeyipo IP, Raji Y, Emikpe BO, Bolarinwa AF (2011) Effects of nicotine on sperm characteristics and fertility profile in adult male rats: a possible role of cessation. J Reprod Infertil 12:201
Ahmad A, Husain A, Mujeeb M, Khan SA, Najmi AK, Siddique NA, Damanhouri ZA, Anwar F (2013) A review on therapeutic potential of Nigella sativa: a miracle herb. Asian Pac J Trop Biomed 3:337–352
Gökçe A, Oktar S, Koc A, Gonenci R, Yalcinkaya F, Yonden Z, Duru M (2010) Protective effect of thymoquinone in experimental testicular torsion. Urol Int 85:461–465
Ricci G, Catizone A, Esposito R, Pisanti FA, Vietri MT, Galdieri M (2009) Diabetic rat testes: morphological and functional alterations. Andrologia 41:361–368
Mallidis C, Agbaje I, McClure N, Kliesch S (2011) Einfluss des Diabetes mellitus auf die Fertilität des Mannes. Urologe 50:33–37
La Vignera S, Condorelli R, Vicari E, D’Agata R, Calogero AE (2012) Diabetes mellitus and sperm parameters. J Androl 33:145–153
Wankeu-Nya M, Florea A, Bâlici S, Watcho P, Matei H, Kamanyi A (2013) Dracaena arborea alleviates ultra-structural spermatogenic alterations in streptozotocin-induced diabetic rats. BMC Complement Altern Med 13:1–9
Mallick C, Mandal S, Barik B, Bhattacharya A, Ghosh D (2007) Protection of testicular dysfunctions by MTEC, a formulated herbal drug, in streptozotocin induced diabetic rat. Biol Pharm Bull 30:84–90
Khaki A, Fathiazad F, Nouri M, Khaki A, Maleki NA, Khamnei HJ, Ahmadi P (2010) Beneficial effects of quercetin on sperm parameters in streptozotocin-induced diabetic male rats. Phytother Res 24:1285–1291
Chaiyasut C, Kusirisin W, Lailerd N, Lerttrakarnnon P, Suttajit M, Srichairatanakool S (2011) Effects of phenolic compounds of fermented Thai indigenous plants on oxidative stress in streptozotocin-induced diabetic rats. Evid Based Complement Alternat Med. https://doi.org/10.1155/2011/749307
Gauthaman K, Adaikan PG, Prasad RN (2002) Aphrodisiac properties of Tribulus terrestris extract (Protodioscin) in normal and castrated rats. Life Sci 71:1385–1396
Kougan GB, Miyamoto T, Tanaka C, Paululat T, Mirjolet JF, Duchamp O, Sondengam BL, Lacaille-Dubois MA (2010) Steroidal saponins from two species of Dracaena. J Nat Prod 73:1266–1270
Gupta R, Sharma AK, Dobhal MP, Sharma MC, Gupta RS (2011) Antidiabetic and antioxidant potential of β-sitosterol in streptozotocin-induced experimental hyperglycemia. J Diabetes 3:29–37
Shalaby MA, Hamowieh AR (2010) Safety and efficacy of Zingiber officinale roots on fertility of male diabetic rats. Food Chem Toxicol 48:2920–2924
Sekiwa Y, Kubota K, Kobayashi A (2000) Isolation of novel glucosides related to gingerdiol from ginger and their antioxidative activities. J Agric Food Chem 48:373–377
Kamtchouing P, Fandio GM, Dimo T, Jatsa HB (2002) Evaluation of androgenic activity of Zingiber officinale and Pentadiplandra brazzeana in male rats. Asian J Androl 4:299–302
Pala M, Ugolini D, Ceppi M, Rizzo F, Maiorana L, Bolognesi C, Schilirò T, Gilli G, Bigatti P, Bono R, Vecchio D (2008) Occupational exposure to formaldehyde and biological monitoring of Research Institute workers. Cancer Detect Prev 32:121–126
Gules O, Eren U (2010) The effect of xylene and formaldehyde inhalation on testicular tissue in rats. Asian-australas. J Anim Sci 23:1412–1420
Ye X, Yan W, Xie H, Zhao M, Ying C (2005) Cytogenetic analysis of nasal mucosa cells and lymphocytes from high-level long-term formaldehyde exposed workers and low-level short-term exposed waiters. Mutat Res Genet Toxicol Environ Mutagen 588:22–27
Zhou DX, Qiu SD, Zhang J, Tian H, Wang HX (2006) The protective effect of vitamin E against oxidative damage caused by formaldehyde in the testes of adult rats. Evid Based Complement Alternat Med 8:584–588
Ozen OA, Yaman M, Sarsilmaz M, Songur A, Kus I (2007) Testicular zinc, copper and iron concentrations in male rats exposed to subacute and subchronic formaldehyde gas inhalation. J Trace Elem Med Biol 16:119–122
Cheng G, Shi Y, Sturla SJ, Jalas JR, McIntee EJ, Villalta PW, Wang M, Hecht SS (2003) Reactions of formaldehyde plus acetaldehyde with deoxyguanosine and DNA: formation of cyclic deoxyguanosine adducts and formaldehyde cross-links. Chem Res Toxicol 16:145–152
Naghdi M, Maghbool M, Seifalah-Zade M, Mahaldashtian M, Makoolati Z, Kouhpayeh SA, Ghasemi A, Fereydouni N (2016) Effects of common fig (Ficus carica) leaf extracts on sperm parameters and testis of mice intoxicated with formaldehyde. Evid Based Complement Alternat Med. https://doi.org/10.1155/2016/2539127
Zhou D, Zhang J, Wang H (2011) Assessment of the potential reproductive toxicity of long-term exposure of adult male rats to low-dose formaldehyde. Toxicol Ind Health 27:591–598
Perez C, Canal JR, Torres MD (2003) Experimental diabetes treated with Ficus carica extract: effect on oxidative stress parameters. Acta Diabetol 40:3–8
Gonzales C, Rubio J, Gasco M, Nieto J, Yucra S, Gonzales GF (2006) Effect of short-term and long-term treatments with three ecotypes of Lepidium meyenii (MACA) on spermatogenesis in rats. J Ethnopharmacol 103:448–454
Rubio J, Riqueros MI, Gasco M, Yucra S, Miranda S, Gonzales GF (2006) Lepidium meyenii (Maca) reversed the lead acetate induced—damage on reproductive function in male rats. Food Chem Toxicol 44:1114–1122
El-Shahat AE, Gabr A, Meki AR, Mehana ES (2009) Altered testicular morphology and oxidative stress induced by cadmium in experimental rats and protective effect of simultaneous green tea extract. J Morphol. https://doi.org/10.4067/S0717-95022009000300020
Wang L, Xu T, Lei WW, Liu DM, Li YJ, Xuan RJ, Ma JJ (2011) Cadmium-induced oxidative stress and apoptotic changes in the testis of freshwater crab Sinopotamon henanense. PLoS ONE 6:e27853
World Health Organisation (1999) WHO laboratory manual for the examination of human semen and sperm-cervical mucus interaction. Cambridge University Press, Cambridge
Messaoudi I, Banni M, Saïd L, Saïd K, Kerkeni A (2010) Involvement of selenoprotein P and GPx4 gene expression in cadmium-induced testicular pathophysiology in rat. Chem Biol Interact 188:94–101
Nna VU, Ujah GA, Mohamed M, Etim KB, Igba BO, Augustine ER, Osim EE (2017) Cadmium chloride–induced testicular toxicity in male wistar rats; prophylactic effect of quercetin, and assessment of testicular recovery following cadmium chloride withdrawal. Biomed Pharmacother 94:109–123
Haeri S, Minaie B, Amin G, Nikfar S, Khorasani R, Esmaily H, Salehnia A, Abdollahi M (2006) Effect of Satureja khuzestanica essential oil on male rat fertility. Fitoterapia 77:495–499
Sefidkon F, Ahmadi SH (2000) Essential oil of Tanacetum pathenium L. J Essent Oil Res 12:427–428
Lambert RJ, Skandamis PN, Coote PJ, Nychas GJ (2001) A study of the minimum inhibitory concentration and mode of action of oregano essential oil, thymol and carvacrol. J Appl Microbiol 91:453–462
Vardar-Ünlü G, Candan F, Sökmen A, Daferera D, Polissiou M, Sökmen M, Dönmez E, Tepe B (2003) Antimicrobial and antioxidant activity of the essential oil and methanol extracts of Thymus pectinatus Fisch. et Mey. Var. pectinatus (Lamiaceae). J Agric Food Chem 51:63–67
Al-Olayan EM, El-Khadragy MF, Metwally DM, Moneim AE (2014) Protective effects of pomegranate (Punica granatum) juice on testes against carbon tetrachloride intoxication in rats. BMC Complement Altern Med 14:1–9
Jin JL, O’Doherty AM, Wang S, Zheng H, Sanders KM, Yan W (2005) Catsper3 and catsper4 encode two cation channel-like proteins exclusively expressed in the testis. Biol Reprod 73:1235–1242
Li HG, Ding XF, Liao AH, Kong XB, Xiong CL (2007) Expression of CatSper family transcripts in the mouse testis during post-natal development and human ejaculated spermatozoa: relationship to sperm motility. Mol Hum Reprod 13:299–306
Ren D, Navarro B, Perez G, Jackson AC, Hsu S, Shi Q, Tilly JL, Clapham DE (2001) A sperm ion channel required for sperm motility and male fertility. Nature 413:603–609
Sun XH, Zhu YY, Wang L, Liu HL, Ling Y, Li ZL, Sun LB (2017) The Catsper channel and its roles in male fertility: a systematic review. Reprod Biol Endocrinol 15:1–2
Park EH, Do Rim Kim HY, Park SK, Chang MS (2014) Panax ginseng induces the expression of CatSper genes and sperm hyperactivation. Asian J Androl 16:845
Park WS, Shin DY, Yang WM, Chang MS, Park SK (2007) Korean ginseng induces spermatogenesis in rats through the activation of cAMP-responsive element modulator (CREM). Fertil Steril 88:1000–1002
Association Practice Committee of the American Society for Reproductive Medicine (2004) Report on optimal evaluation of the infertile male. Fertil Steril 82(Suppl 1):S123–S130
Huang BM, Hsiao KY, Chuang PC, Wu MH, Pan HA, Tsai SJ (2004) Upregulation of steroidogenic enzymes and ovarian 17β-estradiol in human granulosa-lutein cells by Cordyceps sinensis mycelium. Biol Reprod 70:1358–1364
Hsu CC, Tsai SJ, Huang YL, Huang BM (2003) Regulatory mechanism of Cordyceps sinensis mycelium on mouse Leydig cell steroidogenesis. FEBS Lett 543:140–143
Huang YL, Leu SF, Liu BC, Sheu CC, Huang BM (2004) In vivo stimulatory effect of Cordyceps sinensis mycelium and its fractions on reproductive functions in male mouse. Life Sci 75:1051–1062
Li SP, Li P, Dong TT, Tsim KW (2001) Anti-oxidation activity of different types of natural Cordyceps sinensis and cultured Cordyceps mycelia. Phytomedicine 8:207–212
Lin WH, Tsai MT, Chen YS, Hou RC, Hung HF, Li CH, Wang HK, Lai MN, Jeng KC (2007) Improvement of sperm production in subfertile boars by Cordyceps militaris supplement. Am J Chin Med 35:631–641
Jung SW, Kim HJ, Lee BH, Choi SH, Kim HS, Choi YK, Kim JY, Kim ES, Hwang SH, Lim KY, Kim HC (2015) Effects of Korean Red Ginseng extract on busulfan-induced dysfunction of the male reproductive system. Am J Chin Med 39:243–249
Nah SY, Kim DH, Rhim H (2007) Ginsenosides: are any of them candidates for drugs acting on the central nervous system? CNS Drug Rev 13:381–404
Hwang SH, Shin TJ, Choi SH, Cho HJ, Lee BH, Pyo MK, Lee JH, Kang J, Kim HJ, Park CW, Shin HC (2012) Gintonin, newly identified compounds from ginseng, is novel lysophosphatidic acids-protein complexes and activates G protein-coupled lysophosphatidic acid receptors with high affinity. Mol Cells 33:151–162
Choi SH, Shin TJ, Lee BH, Hwang SH, Kang J, Kim HJ, Park CW, Nah SY (2011) An edible gintonin preparation from ginseng. J Ginseng Res 35:471
Barlow P, Delvigne A, Dromme JV, Hoeck JV, Vandenbosch K, Leroy F (1991) Predictive value of classical and automated sperm analysis for in-vitro fertilization. Hum Reprod 6:1119–1124
Liu J, Liang P, Yin C, Wang T, Li H, Li Y, Ye Z (2004) Effects of several Chinese herbal aqueous extracts on human sperm motility in vitro. Andrologia 36:78–83
Fedder MD, Jakobsen HB, Giversen I, Christensen LP, Parner ET, Fedder J (2014) An extract of pomegranate fruit and galangal rhizome increases the numbers of motile sperm: a prospective, randomised, controlled, double-blinded trial. PLoS ONE 9:e108532
Lenzi A, Lombardo F, Sgrò P, Salacone P, Caponecchia L, Dondero F, Gandini L (2003) Use of carnitine therapy in selected cases of male factor infertility: a double-blind crossover trial. Fertil steril 79:292–300
Kefer JC, Agarwal A, Sabanegh E (2009) Role of antioxidants in the treatment of male infertility. Int J Urol 16:449–457
Kruger TF, Coetzee K (1999) The role of sperm morphology in assisted reproduction. Hum Reprod Update 5:172–178
Sambandan TG, Rha C, Kadir AA, Aminudim N, Saad JM, inventors; Malaysia Government of, Massachusetts Institute of Technology, assignee (2006) Bioactive fraction of Eurycoma longifolia. United States patent US 7,132,117
Tambi MI (2003) Glycoprotein water-soluble extract of Eurycoma longifolia Jack as a health supplement in management of healthy aging in aged men. Aging Male 6:41–70
Tambi MI (2003) Water soluble extract of Eurycoma longifolia in enhancing testosterone in males. In: Proceeding of International Trade Show and Conference, Supply Side West, The Venetian, Las Vegas, pp 1–3
Tambi MI (2005) Standardized water soluble extract of Eurycoma longifolia (LJ100) on men’s health. Int J Androl 28:25–44
Tambi MI (2006) Standardized water soluble extract of Eurycoma longifolia (LJ199) maintains healthy aging in man. Aging Male 9:53
Tambi MI, Kadir AA (2006) Eurycoma Longifolia jack: a potent adaptogen in the form of water-soluble extract with the effect of maintaining men’s health. Asian J Androl 8(Suppl 1):49–50
Tambi MI, Imran MK (2010) Eurycoma longifolia Jack in managing idiopathic male infertility. Asian J Androl 12:376
Hussain SA, Hameed A, Nasir F, Wu Y, Suleria HA, Song Y (2018) Evaluation of the spermatogenic activity of polyherbal formulation in oligospermic males. Biomed Res Int. https://doi.org/10.1155/2018/2070895
Mkrtchyan A, Panosyan V, Panossian A, Wikman G, Wagner H (2005) A phase I clinical study of Andrographis paniculata fixed combination Kan Jang™ versus ginseng and valerian on the semen quality of healthy male subjects. Phytomedicine 12:403–409
Ghafouri-Fard S, Shoorei H, Mohaqiq M, Haidar Abbas Raza S, Taheri M (2021) The role of different compounds on the integrity of blood-testis barrier: a concise review based on in vitro and in vivo studies. Gene 780:145531
Takahashi K, Nagahori K, Qu N, Kuramasu M, Hirayanagi Y, Hayashi S, Ogawa Y, Hatayama N, Terayama H, Suyama K, Hirai S, Sakabe K, Itoh M (2019) The effectiveness of traditional Japanese medicine Goshajinkigan in irradiation-induced aspermatogenesis in mice. BMC Complement Altern Med 19:362
Ma B, Zhang J, Zhu Z, Bao X, Zhang M, Ren C, Zhang Q (2019) Aucubin, a natural iridoid glucoside, attenuates oxidative stress-induced testis injury by inhibiting JNK and CHOP activation via Nrf2 up-regulation. Phytomedicine 64:153057
Bae WJ, Zhu GQ, Choi SW, Jeong HC, Bashraheel F, Kim KS, Kim SJ, Cho HJ, Ha U, Hong SH, Lee JY (2017) Antioxidant and antifibrotic effect of a herbal formulation in vitro and in the experimental andropause via Nrf2/HO-1 signaling pathway. Oxid Med Cell Longev. https://doi.org/10.1155/2017/6024839
Jang H, Bae WJ, Kim SJ, Cho HJ, Yuk SM, Han DS, Youn CS, Kwon EB, Hwang SY, Kim SW (2017) The herbal formula KH-204 is protective against erectile dysfunction by minimizing oxidative stress and improving lipid profiles in a rat model of erectile dysfunction induced by hypercholesterolaemia. BMC Complement Altern Med 17:1–1
Fatma BA, Nozha CF, Ines D, Hamadi A, Basma H, Leila AK (2009) Sperm quality improvement after date seed oil in vitro supplementation in spontaneous and induced oxidative stress. Asian J Androl 11:393
Benavente-Garcia O, Castillo J (2008) Update on uses and properties of citrus flavonoids: new findings in anticancer, cardiovascular, and anti-inflammatory activity. J Agric Food Chem 56:6185–6205
El Arem A, Lahouar L, Saafi EB, Thouri A, Ghrairi F, Houas Z, Neffati F, Achour L (2017) Dichloroacetic acid-induced testicular toxicity in male rats and the protective effect of date fruit extract. BMC Pharmacol Toxicol 18:1–9
Hong YJ, Tomas-Barberan FA, Kader AA, Mitchell AE (2006) The flavonoid glycosides and procyanidin composition of Deglet Noor dates (Phoenix dactylifera). J Agric Food Chem 54:2405–2411
Szymonik-Lesiuk S, Czechowska G, Stryjecka-Zimmer M, Słomka M, MĄldro A, Celiński K, Wielosz M (2003) Catalase, superoxide dismutase, and glutathione peroxidase activities in various rat tissues after carbon tetrachloride intoxication. J Hepatobiliary Pancreat Surg 10:309–315
Tabatabaie T, Floyd RA (1994) Susceptibility of glutathione peroxidase and glutathione reductase to oxidative damage and the protective effect of spin trapping agents. Arch Biochem Biophys 314:112–119
Niki E, Yoshida Y, Saito Y, Noguchi N (2005) Lipid peroxidation: mechanisms, inhibition, and biological effects. Biochem Biophys Res Commun 338:668–676
Manna P, Sinha M, Sil PC (2006) Aqueous extract of Terminalia arjuna prevents carbon tetrachloride induced hepatic and renal disorders. BMC Complement Altern Med 6:1–10
Raja S, Ahamed KN, Kumar V, Mukherjee K, Bandyopadhyay A, Mukherjee PK (2007) Antioxidant effect of Cytisus scoparius against carbon tetrachloride treated liver injury in rats. J Ethnopharmacol 109:41–47
Shah NA, Khan MR (2017) Increase of glutathione, testosterone and antioxidant effects of Jurenia dolomiaea on CCl 4 induced testicular toxicity in rat. BMC Complement Altern Med 17:1–9
Khan MR, Ahmed D (2009) Protective effects of Digera muricata (L.) Mart. on testis against oxidative stress of carbon tetrachloride in rat. Food Chem Toxicol 47:1393–1399
Sahreen S, Khan MR, Khan RA (2013) Ameliorating effect of various fractions of Rumex hastatus roots against hepato-and testicular toxicity caused by CCl4. Oxid Med Cell Longev. https://doi.org/10.1155/2013/325406
Shah NA, Khan MR, Naz K, Khan MA (2014) Antioxidant potential, DNA protection, and HPLC-DAD analysis of neglected medicinal Jurinea dolomiaea roots. BioMed Res Int. https://doi.org/10.1155/2014/726241
Lamas CD, Cuquetto Leite L, do Nascimento da Silva E, Thomazini BF, Cordeiro GD, Predes FD, Gollücke AP, Dolder H (2017) Grape juice concentrate alleviates epididymis and sperm damage in cadmium-intoxicated rats. Int J Exp Pathol 98:86–99
Ola-Mudathir KF, Suru SM, Fafunso MA, Obioha UE, Faremi TY (2008) Protective roles of onion and garlic extracts on cadmium-induced changes in sperm characteristics and testicular oxidative damage in rats. Food Chem Toxicol 46:3604–3611
Fraga CG, Galleano M, Verstraeten SV, Oteiza PI (2010) Basic biochemical mechanisms behind the health benefits of polyphenols. Mol Asp Med 31:435–445
García MM, Acquier A, Suarez G, Gomez NV, Gorostizaga A, Mendez CF, Paz C (2012) Cisplatin inhibits testosterone synthesis by a mechanism that includes the action of reactive oxygen species (ROS) at the level of P450scc. Chem Biol Interact 199:185–191
Abilash VG (2017) Protective effect of curcumin on cisplatin-induced genotoxicity in human leukocytes culture. Int J Green Pharm (IJGP) 11(02)
Azu OO, Francis I, Abraham A, Crescie C, Stephen O, Abayomi O (2010) Protective agent, Kigelia Africana fruit extract, against cisplatin-induced kidney oxidant injury in Sprague-Dawley rats. Asian J Pharma Clin Res 3:84
Afsar T, Razak S, Almajwal A (2017) Acacia hydaspica ethyl acetate extract protects against cisplatin-induced DNA damage, oxidative stress and testicular injuries in adult male rats. BMC Cancer 17:1–4
Zhang C, Wang A, Sun X, Li X, Zhao X, Li S, Ma A (2013) Protective effects of Lycium barbarum polysaccharides on testis spermatogenic injury induced by bisphenol A in mice. Evid Based Complement Alternat Med. https://doi.org/10.1155/2013/690808
Luo Q, Yan J, Cui XY (2011) Antaginistic effect of LBP on damage of reproductive system induced by sub-chronic partial 60Co γ-ray radiation in male rats. China J Public Health 27(10):1358–1359
Sharma P, Parmar J, Verma P, Goyal PK (2011) Radiation-induced testicular injury and its amelioration by tinospora cordifolia (an Indian medicinal plant) extract. Evid Based Complement Alternat Med. https://doi.org/10.1155/2011/643847
Prabhakar KR, Veerapur VP, Bansal P, Parihar VK, Kandadi MR, Kumar PB, Priyadarsini KI, Unnikrishnan MK (2007) Antioxidant and radioprotective effect of the active fraction of Pilea microphylla (L.) ethanolic extract. Chem Biol Interact 165:22–32
Li HB, Wong CC, Cheng KW, Chen F (2008) Antioxidant properties in vitro and total phenolic contents in methanol extracts from medicinal plants. LWT-Food Sci Technol 41:385–390
Ajah PO, Eteng MU (2010) Phytochemical screening and histopathological effects of single acute dose administration of Artemisia annua L. on testes and ovaries of Wistar rats. Afr J Biochem Res 4:179–185
Olasantan OD, Areola JO, Ayannuga OA, Babalola O (2015) Evaluation of the gonadoprotective effects of Allanblackia floribundaOliver (Clusiacea) on testes and accessory organs of Wistar rats. J Med Biol Sci Res 1:134–144
Liaudanskas M, Viškelis P, Raudonis R, Kviklys D, Uselis N, Janulis V (2014) Phenolic composition and antioxidant activity of Malus domestica leaves. Sci World J. https://doi.org/10.1155/2014/306217
Cele ND, Sangweni NF, Mosa RA, Penduka D, Lazarus GG, Singh M, Zharare GE, Opoku AR (2017) Testicular dysfunction ameliorative effect of the methanolic roots extracts of Maytenus procumbens and Ozoroa paniculosa. Evid Based Complement Alternat Med. https://doi.org/10.1155/2017/8204816
Akomolafe SF, Oboh G, Akindahunsi AA, Afolayan AJ (2015) Antiperoxidative activity of Tetracarpidium conophorum leaf extract in reproductive organs of male rats. Evid Based Complement Alternat Med. https://doi.org/10.1155/2015/798491
Ayoola AO, Akinloye O, Oguntibeju OO, Oke JM, Odetola AA (2011) Antioxidant activities of Parquetina nigrescens. Afr J Biotechnol 10:4920–4925
Anger JT, Gilbert BR, Goldstein MA (2003) Cryopreservation of sperm: indications, methods and results. J Urol 170:1079–1084
Nallella KP, Sharma RK, Allamaneni SS, Aziz N, Agarwal A (2004) Cryopreservation of human spermatozoa: comparison of two cryopreservation methods and three cryoprotectants. Fertil Steril 82:913–918
Jahromi MA, Movahedin M, Amanloo M, Javad S, Mowla ZM, Batouli H (2013) The effects of calligonum extract on sperm parameters and the rate of apoptosis in aged male mice testis issue. Modares J Med Sci Pathobiol 16:41–54
Tasnim EE, Mohammad Esmael S (2015) Antioxidant effects of brown algae Sargassum on sperm parameters. Medicin 94:e1938
Tierney MS, Croft AK, Hayes MA (2010) Review of antihypertensive and antioxidant activities in macroalgae. Bot Mar. https://doi.org/10.1515/bot.2010.044
Alkan I, Simsek F, Haklar G, Kervancioglu E, Ozveri H, Yalcin S, Akdas A (1997) Reactive oxygen species production by the spermatozoa of patients with idiopathic infertility: relationship to seminal plasma antioxidants. J Urol 157:140–143
Sahin K, Orhan C, Akdemir F, Tuzcu M, Gencoglu H, Sahin N, Turk G, Yilmaz I, Ozercan IH, Juturu V (2016) Comparative evaluation of the sexual functions and NF-κB and Nrf2 pathways of some aphrodisiac herbal extracts in male rats. BMC Complement Altern Med 16:1–1
Hardy MP, Gao HB, Dong Q, Ge R, Wang Q, Chai WR, Feng X, Sottas C (2005) Stress hormone and male reproductive function. Cell Tissue Res 322:147–153
Shukla KK, Mahdi AA, Ahmad MK, Jaiswar SP, Shankwar SN, Tiwari SC (2010) Mucuna pruriens reduces stress and improves the quality of semen in infertile men. Evid based Complement Altern Med 7:137–144
Sato Y, Suzuki N, Horita H, Wada H, Shibuya A, Adachi H, Tsukamoto T, Kumamoto Y, Yamamoto M (1996) Effects of long-term psychological stress on sexual behavior and brain catecholamine levels. J Androl 17:83–90
Misra L, Wagner H (2007) Extraction of bioactive principles from Mucuna pruriens seeds. Indian J Biochem Biophys 44:56–60
Billig H, Furuta I, Rivier C, Tapanainen J, Parvinen M, Hsueh AJ (1995) Apoptosis in testis germ cells: developmental changes in gonadotropin dependence and localization to selective tubule stages. Endocrinology 136:5–12
Hala AH, Khattab ZA, Abdallah G, Kamel M (2010) Grape seed extract alleviate reproductive toxicity caused by aluminium chloride in male rats. J Am Sci 6:352–361
Modaresi M, Khodaii H, Khodadadi A (2013) Effect of Aloe vera extract on spermatogenesis and reproductive hormones in mice. Anim Biol J 69–76
Abd El Tawab AM, Shahin NN, AbdelMohsen MM (2014) Protective effect of Satureja montana extract on cyclophosphamide-induced testicular injury in rats. Chem Biol Interact 224:196–205
Bayatli F, Akkuş D, Kilic E, Saraymen R, Sönmez MF (2013) The protective effects of grape seed extract on MDA, AOPP, apoptosis and eNOS expression in testicular torsion: an experimental study. World J Urol 31:615–622
Bae WJ, Ha US, Kim KS, Kim SJ, Cho HJ, Hong SH, Lee JY, Wang Z, Hwang SY, Kim SW (2014) Effects of KH-204 on the expression of heat shock protein 70 and germ cell apoptosis in infertility rat models. BMC Complement Altern Med 14:1–9
Thakur M, Bhargava S, Praznik W, Loeppert R, Dixit VK (2009) Effect of Chlorophytum borivilianum Santapau and Fernandes on sexual dysfunction in hyperglycemic male rats. Chin J Integr Med 15:448–453
Chatterjee K, Ali KM, De D, Bera TK, Jana K, Maiti S, Ghosh A, Samanta R, Ghosh D (2012) Diabetes induced testicular dysfunction amelioration by ethyl acetate fraction of hydromethanolic extract of root of Musa paradisiaca L. in streptozotocin-induced diabetic rat. Asian Pac J Trop Dis 2:S233-241
Mallick C, Bera TK, Ali KM, Chatterjee K, Ghosh D (2010) Diabetes-induced testicular disorders vis-a-vis germ cell apoptosis in albino rat: remedial effect of hexane fraction of root of Musa paradisiaca and leaf of Coccinia indica. J Health Sci 56:641–654
Kanter M, Aktas C, Erboga M (2013) Curcumin attenuates testicular damage, apoptotic germ cell death, and oxidative stress in streptozotocin-induced diabetic rats. Mol Nutr Food Res 57:1578–1585
Roy S, Rahaman N, Ahmed F, Metya S, Sannigrahi S (2013) Naringenin attenuates testicular damage, germ cell death and oxidative stress in streptozotocin induced diabetic rats: naringenin prevents diabetic rat testicular damage. J Appl Biomed 11:195–208
Kanter M, Aktas C, Erboga M (2012) Protective effects of quercetin against apoptosis and oxidative stress in streptozotocin-induced diabetic rat testis. Food Chem Toxicol 50:719–725
Yu W, Wan Z, Qiu XF, Chen Y, Dai YT (2013) Resveratrol, an activator of SIRT1, restores erectile function in streptozotocin-induced diabetic rats. Asian J Androl 15:646
Long L, Wang J, Lu X, Xu Y, Zheng S, Luo C, Li Y (2015) Protective effects of scutellarin on type II diabetes mellitus-induced testicular damages related to reactive oxygen species/Bcl-2/Bax and reactive oxygen species/microcirculation/staving pathway in diabetic rat. J Diabetes Res. https://doi.org/10.1155/2015/252530
Shi GJ, Zheng J, Wu J, Qiao HQ, Chang Q, Niu Y, Sun T, Li YX, Yu JQ (2017) Beneficial effects of Lycium barbarum polysaccharide on spermatogenesis by improving antioxidant activity and inhibiting apoptosis in streptozotocin-induced diabetic male mice. Food Funct 8:1215–1226
Helpap B (1980) The biological significance of atypical hyperplasia of the prostate. Virchows Archiv A 387:307–317
Elberry AA, Mufti ST, Al-Maghrabi JA, Abdel-Sattar EA, Ashour OM, Ghareib SA, Mosli HA (2011) Anti-inflammatory and antiproliferative activities of date palm pollen (Phoenix dactylifera) on experimentally-induced atypical prostatic hyperplasia in rats. J Inflamm 8:1–3
Ebeling L (1986) Therapeutic results of defined pollen extract in patients with chronic prostatitis or BPH accompanied by chronic prostatitis. Ther Prostatitis 154–160
Saleh SR, Attia R, Ghareeb DA (2018) The ameliorating effect of berberine-rich fraction against gossypol-induced testicular inflammation and oxidative stress. Oxid Med Cell Longev. https://doi.org/10.1155/2018/1056173
Li Z, Geng YN, Jiang JD, Kong WJ (2014) Antioxidant and anti-inflammatory activities of berberine in the treatment of diabetes mellitus. Evid Based Complement Alternat Med. https://doi.org/10.1155/2014/289264
Al-Azemi M, Omu FE, Kehinde EO, Anim JT, Oriowo MA, Omu AE (2010) Lithium protects against toxic effects of cadmium in the rat testes. J Assist Reprod Genet 27:469–476
Abd-Allah AR, Helal GK, Al-Yahya AA, Aleisa AM, Al-Rejaie SS, Al-Bakheet SA (2009) Pro-inflammatory and oxidative stress pathways which compromise sperm motility and survival may be altered by L-carnitine. Oxid Med Cell Longev 2:73–81
Sofikitis N, Giotitsas N, Tsounapi P, Baltogiannis D, Giannakis D, Pardalidis N (2008) Hormonal regulation of spermatogenesis and spermiogenesis. J Steroid Biochem Mol Biol 109:323–330
Schlatt S, Ehmcke J (2014) Regulation of spermatogenesis: an evolutionary biologist’s perspective. Semin Cell Dev Biol 29:2–16
Low BS, Das PK, Chan KL (2013) Standardized quassinoid-rich Eurycoma longifolia extract improved spermatogenesis and fertility in male rats via the hypothalamic–pituitary–gonadal axis. J Ethnopharmacol 145:706–714
Simpson BJ, Wu FC, Sharpe RM (1987) Isolation of human Leydig cells which are highly responsive to human chorionic gonadotropin. J Clin Endocrinol 65:415–422
Ishak KG, Zimmerman HJ (1987) Hepatotoxic effects of the anabolic/androgenic steroids. Semin Liver Dis 7:230–236
Sheckter CB, Matsumoto AM, Bremner WJ (1989) Testosterone administration inhibits gonadotropin secretion by an effect directly on the human pituitary. J Clin Endocrinol Metab 68:397–401
Zhu Z, Li L, Jin X, Fang J, Zhang D (2014) Er-Xian Decoction, a traditional Chinese herbal formula, intervening early in hypothalamic-pituitary axis of male rats with delayed puberty. Pharmacogn Mag 10:517–521
Mushtaq T, Wales J (2007) Diagnosis, investigation and treatment of delayed puberty in children. Paediatr Child Health 17:349–355
Rolf C, Nieschlag E (1998) Potential adverse effects of long-term testosterone therapy. Bailliere’s Clin Endocrinol Metab 12:521–534
Moundipa PF, Beboyl NS, Zelefack F, Ngouela S, Tsamo E, Schill WB, Monsees TK (2005) Effects of Basella alba and Hibiscus macranthus extracts on testosterone production of adult rat and bull Ley dig cells. Asian J Androl 7:411–417
Watcho P, Kamtchouing P, Sokeng SD, Moundipa PF, Tantchou J, Essame JL, Koueta N (2004) Androgenic effect of Mondia whitei roots in male rats. Asian J Androl 6:269–272
Mbongue FG, Kamtchouing P, Essame OJ, Yewah PM, Dimo T, Lontsi D (2005) Effect of the aqueous extract of dry fruits of Piper guineense on the reproductive function of adult male rats. Indian J Pharmacol 37(1):30
Sherins RJ, Hodgen GD (1976) Testicular gamma glutamyl-transpeptidase: an index of Sertoli cell function in man. J Reprod Fertil 48:191–193
Peiris LD, Dhanushka MA, Jayathilake TA (2015) Evaluation of aqueous leaf extract of Cardiospermum halicacabum (L.) on fertility of male rats. Biomed Res Int. https://doi.org/10.1155/2015/175726
Viji M, Murugesan S (2010) Phytochemical analysis and antibacterial activity of medicinal plant Cardiospermum halicacabum Linn. J Phytol 2:68–77
Hong MY, Seeram NP, Heber D (2008) Pomegranate polyphenols down-regulate expression of androgen-synthesizing genes in human prostate cancer cells overexpressing the androgen receptor. J Nutr Biochem 19:848–855
Kurhekar JV (2021) Ancient and modern practices in phytomedicine. In: Preparation of Phytopharmaceuticals for the Management of Disorders. Elsevier, pp 55–75
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Ramgir, S.S., Renu, K., Vellingiri, B. et al. Phytomedicinal therapeutics for male infertility: critical insights and scientific updates. J Nat Med 76, 546–573 (2022). https://doi.org/10.1007/s11418-022-01619-0
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DOI: https://doi.org/10.1007/s11418-022-01619-0
Keywords
- Male infertility
- Reproductive dysfunctions
- Medicinal plants
- Infertility management
- Spermatogenesis