Hostname: page-component-77c89778f8-m8s7h Total loading time: 0 Render date: 2024-07-20T09:09:51.974Z Has data issue: false hasContentIssue false
  • English
  • Français

Mucuna pruriens seed powder feeding influences reproductive conditions and development in Japanese quail Coturnix coturnix japonica

Published online by Cambridge University Press:  28 October 2008

S. K. Prasad ,
T. N. Qureshi  and
S. Qureshi
S. K. Prasad*
Affiliation:
School of Studies in Zoology and Biotechnology, Vikram University, Ujjain 456010, India
T. N. Qureshi
Affiliation:
School of Studies in Zoology and Biotechnology, Vikram University, Ujjain 456010, India
S. Qureshi
Affiliation:
School of Studies in Zoology and Biotechnology, Vikram University, Ujjain 456010, India
*
E-mail: drskprasad2006@rediffmail.com
Get access

Abstract

This study was designed to test whether Mucuna pruriens, a natural source of l-dihydroxyphenylalanine (l-DOPA, a dopamine precursor) feeding, can influence development and reproductive conditions in the high food value bird, Japanese quail, Coturnix coturnix japonica. Experiments were performed in both male and female Japanese quail. One-week-old quail chicks were divided into three groups of 36 birds each. Group I was provided with normal diet and served as control. Group II was provided with food mixed with l-DOPA (50 mg/15 g food) and Group III was provided with food mixed with M. pruriens seed powder (480 g/kg food). At the age of 3 weeks (when birds were sexually distinguished) Group I was divided into two sub-groups IA (male) and IB (female) of six birds each. Similarly, Groups II and III were sub-divided into IIA (male), IIB (female) and IIIA (male), IIIB (female), respectively, of six birds each. Observations were made up to the age of 5 weeks. Male experimental groups (IIA and IIIA) showed significantly increased testicular activity, cloacal gland volume, body weight (BW), plasma testosterone and LH level in comparison to control (IA). Similarly female experimental groups (IIB and IIIB) showed significantly greater weight of reproductive organs (uterus, ovary, oviduct and ovarian follicle), BW, egg weight and size and number of follicles. On the other hand, plasma prolactin level was significantly low in comparison to control (IB). Results suggest that M. pruriens is a rich natural source of l-DOPA and the development and reproduction in Japanese quail might be associated with the dopaminergic system of the brain.

Keywords

reproductionMucuna pruriensl-DOPAnutritionJapanese quail
Type
Full Paper
Information
animal , Volume 3 , Issue 2 , February 2009 , pp. 261 - 268
Copyright
Copyright © The Animal Consortium 2008

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Bhatt, R, Chaturvedi, CM 1993. l-DOPA treatment induces scotosensitivity in Japanese quail. Journal of Reproductive Biology and Comparative Endocrinology 5, 75–83.Google Scholar
Boswell, T, Sharp, PJ, Hall, MR, Goldsmith, AR 1995. Migratory fat deposition in European quail: a role of prolactin. Journal of Endocrinology 146, 71–79.CrossRefGoogle Scholar
Bruning, JL, Kintz, BL 1977. Computational handbook of statistics, 2nd edition. Scott, Foresman and Company, Glenview, IL.Google Scholar
Chastel, O, Barbrand, C, Weimerskirch, H, Lormee, H, Lacroix, A, Tostain, O 2005. High level of LH and testosterone in a tropical seabird with an elaborate courtship display. General and Comparative Endocrinology 140, 33–40.CrossRefGoogle Scholar
Chaturvedi, CM, Bhatt, R 1990. The effect of different temporal relationships of 5-hydroxytryptophan (5-HTP) and l-dihydroxyphenylalanine (l-DOPA) on reproductive and metabolic response of migratory red headed bunting (Emberiza bruniceps). Journal of Interdisciplinary Cycle Research 21, 129–139.CrossRefGoogle Scholar
Chaturvedi, CM and Meier, AH 1988. Neurotransmitter affecting drugs reset relative photorefractoriness in Japanese quail. Proceedings of the 4th International Symposium on Avian Endocrinology, Tokyo, Japan, p. 122.Google Scholar
Chaturvedi, CM, Prasad, SK 1991. Timed daily injections of neurotransmitter precursors alter the gonad and body weights of spotted munia, Lonchura Punctulata, maintained under short daily photoperiods. Journal of Experimental Zoology 260, 194–201.CrossRefGoogle Scholar
Chaturvedi, CM, Bhatt, R, Prasad, SK 1994. Effect of timed administration of neurotransmitter activity on body weight and plumage pigmentation in the Lal munia, Estrilda amandava. Indian Journal of Experimental Biology 32, 238–242.Google Scholar
El Halawani, ME, Youngren, OM, Silsby, JL, Phillips, RE 1991. Involvement of dopamine in prolactin release induced by electrical stimulation of the hypothalamus of the female turkey Meleagris gallopavo. General and Comparative Endocrinology 84, 360–364.CrossRefGoogle ScholarPubMed
Fehrer, SC 1984. The role of monoamines and thyrotropin releasing hormone in prolactin and luteinizing hormone release by the pituitary gland of the young domestic turkey Meleagris gallopavo. PhD, University of Minnesota, MN.Google Scholar
Forman, LJ, Sonntog, WE, Miki, N, Meites, J 1980. Maintenance by l-DOPA treatment of estrous cycle and LH response to estrogen in aging female rats. Experimental Aging Research 6, 547–554.CrossRefGoogle ScholarPubMed
Hall, TR, Chadwick, A 1983. Hypothalamic control of prolactin and growth hormone secretion in the pituitary gland of the pigeon and the chicken: in vitro studies. General and Comparative Endocrinology 49, 135–143.CrossRefGoogle ScholarPubMed
Hall, TR, Chadwick, A 1984. Dopaminergic inhibition of prolactin release from pituitary gland of the domestic fowl incubated in vitro. Journal of Endocrinology 103, 63–69.CrossRefGoogle ScholarPubMed
Harvey, S, Chadwick, A, Border, G, Scanes, CG, Phillips, TG 1982. Neuroendocrine control of prolactin secretion. In Aspects of avian endocrinology: practical and theoretical implications (ed. CG Scanes, MA Ottinger, AD Kenny, J Balthazart, J Cronshaw and IC Jones), pp. 41–64. Texas Tech. Press, Lubbock, TX.Google Scholar
Huang, HH, Meites, J 1975. Reproductive capacity of aging female rats. Neuroendocrinology 17, 289–295.CrossRefGoogle ScholarPubMed
Jimenez, AE, Voogt, LL, Carr, LA 1978. l-3, 4-dihydroxyphenylalanine (l-DOPA) as an inhibitor of prolactin release. Endocrinology 102, 166–174.CrossRefGoogle ScholarPubMed
Katzenschlager, R, Evans, A, Manson, A, Patsalos, PN, Ratnaraj, N, Watt, H, Timmermann, L, Van der Giessen, R, Lees, AJ 2004. Mucuna pruriens in Parkinson’s disease: a double blind clinical and pharmacological study. Journal of Neurology, Neurosurgery and Psychiatry 75, 1672–1677.CrossRefGoogle ScholarPubMed
Ketterson, ED, Nolan, V Jr 1999. Adaptation, exaptation, and constraint: a hormonal perspective. The American Naturalist 154, S4–S25.CrossRefGoogle ScholarPubMed
Koch, Y, Lu, KH, Meites, J 1970. Biphasic effects of catecholamines on pituitary prolactin release in vitro. Endocrinology 87, 673–675.CrossRefGoogle ScholarPubMed
Lorenzetti, F, MacIsaac, S, Arnason, JT, Awang, DVC, Buckles, D 1998. The Phytochemistry, toxicology and food potential of velvetbean (Mucuna Adans spp., Fabaceae). In Cover crop in West Africa: contributing to sustainable agriculture (ed. D Buckles, A Etèka, O Osiname, M Galiba and N Galiano), pp. 67–84. International Development Research Centre (IDRC), Ottawa, Canada.Google Scholar
Lu, KH, Huang, HH, Chen, HT, Kurez, N, Miduszewski, R, Meites, J 1977. Positive feed back by estrogen and progesterone on LH release in old and young rats. Proceedings of the Society for Experimental Biology and Medicine 154, 82–85.CrossRefGoogle Scholar
Lubis, IS, Sastrapradha, SHA 1981. l-dihydroxy-phenylalanine (l-DOPA) in Mucuna seeds. Annales Bogorienses 7, 107–114.Google Scholar
Macnamee, MC, Sharp, PJ, Lea, W, Sterling, RJ, Harvey, S 1986. Evidence that vasoactive intestinal peptide is a physiological prolactin-releasing factor in the bantam hen. General and Comparative Endocrinology 62, 470–478.CrossRefGoogle ScholarPubMed
Manyam, B 1995. An alternative medicine treatment for Parkinson’s disease. Journal of Alternative and Complementary Medicine 1, 249–255.Google Scholar
Manyam, BV, Dhanasekaran, M, Hare, TA 2004. Effect of antiparkinson’s drug HP-200 (Mucuna pruriens) on the central monoaminergic neurotransmitters. Phytotherapy Research 18, 97–101.CrossRefGoogle ScholarPubMed
Meites, J, Simpkins, J, Bruni, J, Advis, J 1977. Role of biogenic amines in control of anterior pituitary hormones. IRCS Journal of Medical Science 5, 1–7.Google Scholar
Miller, LJ, Meier, AH 1983. Temporal synergism of neurotransmitter affecting drugs influences seasonal condition in sparrows. Journal of Interdisciplinary Cycle Research 14, 75–84.CrossRefGoogle Scholar
Mueller, GP, Simpkins, J, Moore, KE, Meites, J 1976. Differential effects of dopamine agonists and haloperiodol on release of prolactin, thyroid stimulating hormone, growth hormone and luteinizing hormone in rats. Neuroendocrinology 20, 121–135.CrossRefGoogle Scholar
Norris, DO 1997. Vertebrate endocrinology. Academic Press, San Diego, CA.Google Scholar
Office de Vulgarisation Pharmaceutique (OVP) 1995. Dictionnaire Vidal. OVP-Éditions du Vidal, Paris, France.Google Scholar
Panda, B, Ahuja, SD, Shrivastava, AK, Singh, RP, Agarwal, SK, Thomas, PC 1987. Quail production technology. Central Avian Research Institute, Izatnagar, India.Google Scholar
Parikh, KM, Doshi, VJ, Sawant, SV, Salunkh, UB 1990. Estimation of l-DOPA from the plant Mucuna pruriens and its formulations. Indian Drugs 27, 353–356.Google Scholar
Prasad, SK, Chaturvedi, CM 2006. 12-HR temporal relationship of circadian serotonergic and dopaminergic activity influences seasonal testicular growth and secondary sex characters in Indian weaver bird, Ploceus philippinus. Journal of Experimental Zoology India 9, 27–32.Google Scholar
Prasad, SK, Rathore, K 2004. Effect of neurotransmitter affecting drugs on the activity of median eminence in spotted munia, Lonchura punctulata. Biochemical and Cellular Archives 4, 105–110.Google Scholar
Prasad, SK, Roy, B 2003. Effect of neurotransmitter affecting drugs on body, comb and Wattle growth in sexually immature cockerel. Journal of Experimental Zoology India 6, 285–290.Google Scholar
Prasad, SK, Thakur, SK 2005. Alteration of serum parameters during non-reproduction period by 5-HTP and l-DOPA administration in spotted munia Lonchura punctulata. Journal of Cell and Tissue Research 5, 421–424.Google Scholar
Prasad, SK, Thapliyal, JP, Chaturvedi, CM 1992. The effects of daily injection of l-dihydroxyphenylalanine and 5-hydroxytryptophan in different temporal relationships on thyroid–gonadal interaction in an Indian finch, spotted munia, Lonchura punctulata. General and Comparative Endocrinology 86, 335–343.CrossRefGoogle Scholar
Prasad, SK, Alone, MK, Roy, B 2003. Serum l-thyroxine and LH of 15 days old Cockerel in response to circadian administration of serotonergic and dopaminergic drugs. Biochemical and Cellular Archives 3, 105–108.Google Scholar
Prasad, SK, Thakur, SK, Qureshi Taj, N 2006. 5-HTP and l-DOPA administration at zero and 12-hr interval influences normal blood parameters and whole body oxygen consumption in Indian Garden Lizard, Calotes versicolor. Biochemical and Cellular Archives 6, 317–322.Google Scholar
Quadri, SK, Kledzik, GS, Meites, J 1973. Reinitiation of estrous cycles in old constant estrous rats by central acting drugs. Neuroendocrinology 11, 248–255.CrossRefGoogle ScholarPubMed
Qureshi, TN 2008. Effect of neurotransmitter affecting drugs on development and reproduction of high food value bird, Japanese quail, Coturnix coturnix japonica. PhD, Vikram University, Ujjain, India.Google Scholar
Reed, WL 2000. Maternal effects in the American coot: consequences for offspring growth and survival. PhD, Iowa State University, Ames, IA.Google Scholar
Shaar, CJ, Clemens, JA 1974. The role of catecholamines in the release of anterior pituitary prolactin in vivo. Endocrinology 95, 1202–1212.CrossRefGoogle Scholar
Simpkins, JW, Muller, GP, Huang, HH, Meites, J 1977. Evidence for depressed catecholamine and enhanced serotonin metabolism in aging male rats: possible relation to gonadotropin secretion. Endocrinology 100, 1672–1678.CrossRefGoogle Scholar
Sinervo, B, Basolo, AL 1996. Testing adaptation using phenotypic manipulations. In Adaptation (ed. MR Rose and GV Lauder), pp. 149–185. Academic Press, San Diego, CA.Google Scholar
Su, DR, Tang, DG, Xu, JW, Zhang, X 1992. Determination and extraction of Levodopa in legume of Mucuna cochinchinensis. Tiaran Chanwu Yanji Yu Kairfa 4, 27–30.Google Scholar
Weiner, RI, Ganong, WF 1978. Role of brain monoamines and histamine in regulation of anterior pituitary secretion. Physiological Reviews 58, 905–976.CrossRefGoogle ScholarPubMed
Williams, TD 1999. Avian Reproduction – overview. In Encyclopedia of reproduction (ed. E Knobil and JD Neill), vol. 1, pp. 325–336. Academic Press, San Diego, CA.Google Scholar
Wilson, JM, Meier, AH 1983. Tryptophan feeding induced sensitivity to short daylength in photorefractory hamsters. Neuroendocrinology 36, 59–63.CrossRefGoogle ScholarPubMed
Wilson, JM, Meier, AH 1989. Resseting the annual cycle with timed daily injections of 5-hydroxytryptophan and l-dihydroxyphenylalanine in Syrian hamsters. Chronobiology International 6, 113–132.CrossRefGoogle Scholar
Xu, M, Proudman, JA, Pitts, GR, Wong, EA, Foster, DN, El Halawani, ME 1996. Vasoactive intestinal peptide stimulates prolactin mRNA expression in turkey pituitary cells. Effects of dopaminergic drugs. Proceedings of the Society for Experimental Biology and Medicine 212, 52–62.CrossRefGoogle ScholarPubMed
Youngren, OM, Chaiseha, Y, El Halawani, ME 1998. Regulation of prolactin secretion by dopamine and vasoactive intestinal peptide at the level of the pituitary in the turkey. Neuroendocrinology 68, 319–325.CrossRefGoogle ScholarPubMed
Zhang, X, Su, D, Xu, JW, Tang, DG 1991. New process of extraction of l-DOPA. Zhongguo Yiyao Gongye Zazhi 22, 207–214.Google Scholar