Drug Res (Stuttg) 2016; 66(08): 420-426
DOI: 10.1055/s-0042-108186
Original Article
© Georg Thieme Verlag KG Stuttgart · New York

Reversible Anti-Spermatogenic Effect of Piperine on Epididymis and Seminal Vesicles of Albino Rats

G. Chinta
1   DBT-Interdisciplinary Program in Life Sciences, Pondicherry University, Puducherry, India
,
L. Periyasamy
2   Department of Biochemistry and Molecular Biology, Pondicherry University, Puducherry, India
› Institutsangaben
Weitere Informationen

Publikationsverlauf

received 29. März 2016

accepted 02. Mai 2016

Publikationsdatum:
09. Juni 2016 (online)

Abstract

Background: We have recently proved the interactions of piperine with androgen receptor and androgen binding protein. The present study was aimed to evaluate the antifertility effect of piperine on male albino rats after the treatment period i. e., after 60 days and withdrawal period i. e., after 120 days.

Materials and Methods: Adult male rats were divided into 4 groups (n=12). Group I: Control: Rats were given vehicle p.o i. e., 0.5% carboxy methyl cellulose (CMC) in normal saline daily for 60 days, Group II: Rats were treated with piperine suspended in 0.5% CMC at a dose of 10 mg/kg daily/60 days. Group III: Rats were treated with piperine suspended in 0.5% CMC at a dose of 10 mg/kg on every 4th day for 60 days. Group IV: Rats were treated with piperine suspended in 0.5% CMC at a dose of 10 mg/kg on every 7th day for 60 days.

Results: Piperine significantly altered the epididymal sperm count, motility, viability, weight of the epididymis, cauda, caput, corpus and seminal vesicles. It also exhibited negative impact on biochemical markers via decreasing epididymal sialic acid levels, seminal fructose content, epididymal anti-oxidant enzyme activities of super oxide dismutase (SOD), catalase (CAT) and by increasing the malondialdehyde content after the treatment period. Histopathological observations also supported the above findings. All the altered values were reinforced after the withdrawal period.

Conclusion: From the results of this study, we can conclude that piperine has the potential to become a good lead for the reversible male oral contraceptive research.

 
  • References

  • 1 Rabe T. Contraception - Update and trends. J Reprod Endokrinol 2010; 7: 18-38
  • 2 Stalin C, Vivekanandan C, Bhavya E. Medicinal plants with anti-fertility activity: An overview. Global J Med Res 2013; 13: 1-4
  • 3 Guptha RS, Sharma R. A review on plant exhibiting anti-fertility activities. Nat Prod Rad 2006; 5: 389-410
  • 4 Pasqualotto FF, Lucon AM, Pasqualotto EB et al. Trends in male contraception. Rev Hosp Clin Fac Med Sao Paulo 2003; 58: 275-283
  • 5 Pavankumar S, Gourav L, Deepak KS et al. Anti-fertility activities of traditional medicinal plants in male with emphasis on their mode action: A review. J Glob Sci 2015; 1: 1165-1179
  • 6 Rajandeep K, Anil S, Ravinder K et al. Rising Trends towards Herbal Contraceptives. J Nat Prod & Plant Res 2011; 1: 5-12
  • 7 Johri RK, Zutshi U. An Ayurvedic formulation ‘Trikatu’ and its constituents. J Ethnopharmacol. 1992; 37: 85-91
  • 8 Chinta G, Charles MRC, Klopčič I et al. In Silico and In Vitro Investigation of the Piperineʼs Male Contraceptive Effect: Docking and Molecular Dynamics Simulation Studies in Androgen-Binding Protein and Androgen Receptor. Planta Med 2015; 81: 804-812
  • 9 Kulkarni SK, Bhutani MK, Bishnoi M. Antidepressant activity of curcumin: involvement of serotonin and dopamine system. Psychopharmacol (Berl) 2008; 201: 435-442
  • 10 Li S, Wang C, Wei Wang M et al. Anti-Depressant like effects of piperine in chronic mild-stress treated mice and its possible mechanisms. Life Sci 2007; 80: 1373-1381
  • 11 Li S, Wang C, Li W et al. Antidepressant-like effects of piperine and its derivative, antiepilepsirine. J Asian Nat Prod Res 2010; 9: 421-430
  • 12 Panda S, Kar A. Piperine lowers the serum concentrations of thyroid hormones, glucose and hepatic 5’D activity in adult male mice. Horm Metab Res 2003; 35: 523-526
  • 13 Park BS, Son DJ, Park YH et al. Antiplatelet effects of acidamides isolated from the fruits of Piper longum L. Phytomed 2007; 14: 853-855
  • 14 Atal S, Agrawal RP, Vyas S et al. Evaluation of the effect of piperine per se on blood glucose level in alloxan-induced diabetic mice. Acta Pol Pharm 2012; 69: 965-969
  • 15 Atal S, Atal S, Vyas S et al. Bio-enhancing effect of Piperine with Metformin on lowering blood glucose level in Alloxan induced diabetic mice. Pharmacog Res 2016; 8: 56-60
  • 16 Mujumdar AM, Dhuley JN, Deshmukh VK et al. Anti-inflammatory activity of piperine. Jpn J Med Sci Biol 1990; 43: 95-100
  • 17 Veerareddy PR, Vobalaboina V, Nahid A. Formulation and evaluation of oil-in-water emulsions of piperine in visceral leishmaniasis. Pharmazie 2004; 59: 194-197
  • 18 Samykutty A, Shetty AV, Dakshinamoorthy G et al. Piperine, a Bioactive Component of Pepper Spice Exerts Therapeutic Effects on Androgen Dependent and Androgen Independent Prostate Cancer Cells. PLoS One 2013; 8: e65889
  • 19 Kim SH, Lee YC. Piperine inhibits eosinophil infiltration and airway hyperresponsiveness by suppressing T cell activity and Th2 cytokine production in the ovalbumin-induced asthma model. J Pharm Pharmacol 2009; 61: 353-359
  • 20 El Hamss R, Idaomar M, Alonso-Moraga A et al. Antimutagenic properties of bell and black peppers. Food Chem Toxicol 2003; 41: 41-47
  • 21 Bajad S, Bedi KL, Singla AK et al. Antidiarrhoeal activity of piperine in mice. Planta Med 2001; 67: 284-287
  • 22 Koul IB, Kapil A. Evaluation of the liver protective potential of piperine, an active principle of black and long peppers. Planta Med 1993; 59: 413-417
  • 23 Zhao JQ, Du GZ, Xiong YC et al. Attenuation of beryllium induced hepatorenal dysfunction and oxidative stress in rodents by combined effect of gallic acid and piperine. Arch Pharm Res 2007; 30: 1575-1583
  • 24 Badmadev V, Majid M, Norkus EP. Piperine, An alkaloid derived from Black pepper increases serum response of Beta carotene during14 day Oral Beta carotene supplementation. Nutri Res 1999; 19: 381-388
  • 25 Nirala SK, Bhadauria M, Mathur R et al. Influence of alpha-tocopherol, propolis and piperine on therapeutic potential of tiferron against beryllium induced toxic manifestations. J Appl Toxicol 2008; 28: 44-54
  • 26 Lambert JD, Hong J, Kim DH et al. Piperine enhances the bioavailability of the tea polyphenol (-)-epigallocatechin-3-gallate in mice. J Nutr 2004; 134: 1948-1952
  • 27 Han HK. The effects of black pepper on the intestinal absorption and hepatic metabolism of drugs. Expert Opin Drug Metab Toxicol 2011; 7: 721-729
  • 28 Patil UK, Singh A, Chakraborthy AK. Role of piperine as a Bioavailability Enhancer. Int J Recent Adv In Pharmaceut Res 2011; 4: 16-23
  • 29 Chinta G, Syed SB, Coumar SM et al. Piperine: A Comprehensive review of its preclinical and clinical investigations. Current Bioact Comp 2015; 11: 156-169
  • 30 Malini T, Manimaran RR, Arunakaran J et al. Effects of piperine on testis of albino rats. J Ethnopharmacol 1999; 64: 219-225
  • 31 D’cruz SC, Mathur PP. Effect of piperine on the epididymis of adult male rats. Asian J Androl 2005; 7: 363-368
  • 32 D’Cruz SC, Vaithinathan S, Saradha B et al. Piperine activates testicular apoptosis in adult rats. J Biochem Mol Toxicol 2008; 22: 382-388
  • 33 Piyachaturawat P, Glinsukon T, Toskulkao C. Acute and subacute toxicity of piperine in mice, rats and hamsters. Toxicol Lett 1983; 16: 351-359
  • 34 Gangadharan B, Murugan MA, Mathur PP. Effect of methoxychlor on antioxidant system of goat epididymal sperm in vitro. Asian J Androl 2001; 3: 285-288
  • 35 Cooper TG. WHO Laboratory manual for the examination and processing of human semen. 5 Ed Switzerland: WHO Press; 2010
  • 36 Lombart C, Winzler RJ. Isolation and characterization of canine submaxillary mucin. Biochem J 1972; 128: 975-977
  • 37 Nixon DA. The determination of fructose in biological fluids using anthrone. Clin Chim Acta 1969; 26: 167-169
  • 38 Marklund S, Marklund G. Involvement of the superoxide anion radical in the autoxidation of pyrogallol and a convenient assay for superoxide dismutase. Eur J Biochem 1974; 47: 469-474
  • 39 Sinha AK. Colorimetric assay of catalase. Anal Biochem. 1972; 47: 389-394
  • 40 Devasagayam TP, Tarachand U. Decreased lipid peroxidation in the rat kidney during gestation. Biochem Biophys Res Commun 1987; 145: 134-138
  • 41 Arroteia KF, Garcia PV, Barbieri MF et al. The Epididymis: Embryology, structure, function and its role in fertilization ans infertility. In: Pereira LAV. (ed) Embryolog-updates and highlights on classic topics. University campus Stephri: Intech. 2012: 41-66
  • 42 Marib EN. The Reproductive System. In: Beauparlant S. (Ed) Essentials of Human Anatomy and Physiology. United States: Pearson; 2015: 37
  • 43 Roberts M, Jarvi K. Steps in the investigation and management of low semen volume in the infertile man. Can Urol Assoc J 2009; 3: 479-485
  • 44 Selen S, Tortora GJ, Derrickson BH. The reproductive system. In: Gerrerd J, Tortora Derricson BH. (Ed) Principles of Anatomy and Physiology. USA: John Willey and Sons; 2012: 1029-1064
  • 45 Vetter CM, Miller JE, Crawford LM et al. Comparison of motility and membrane integrity to assess rat sperm viability. Reprod Toxicol 1998; 12: 105-114
  • 46 Anbalagan J, Kanagaraj P, Srinivasan N et al. Effect of polychlorinated bisphenyl, Arachlor 1254 on rat epididymis. Indian J Medical Res 2003; 118: 236-242
  • 47 Joshi SC, Sharma A, Sharma P et al. Contraceptive Efficacy of Citrullus colocynthis Methanolic Extract in Male Rats. American J Phytomed & Clinic Therapeut 2014; 2: 229-241
  • 48 Gupta RS, Kachhawa JB, Chaudhary R. Antifertility effects of methanolic pod extract of Albizzia lebbeck (L.) Benth in male rats. Asian J Androl 2004; 6: 155-159
  • 49 Olayinka E, Ore A. Hepatotoxicity, nephrotoxicity and oxidative Stress in rat testis following exposure to Haloxyfop-p-methyl ester, an Aryloxyphenoxypropionate herbicide. Toxics 2015; 3: 373-389
  • 50 Ghiasi Ghalehkandi J, Hassanpour S, Issabeagloo E et al. Assessment of the effects of red onion (Allium cepa Linn) juice on semen oxidative status compared to Zn sulfate in rats. Animal reproduction 2015; 12: 298-304
  • 51 Abarikwu SO, Otuechere CA, Ekor M et al. Ameliorates Cyclophosphamide-induced Reproductive Toxicity in Male Rats. Toxicol Int 2012; 19: 207-214
  • 52 Alagammal M, Sakthidevi G, Mohan VR. Anti-fertility activity of whole plant extracts of Polygola rosmanifolia wight & Arn against male albino rats. Journal of advanced pharmaceutical sciences 2013; 3: 386-393