Effect of Gonadotrophins and Gonadotrophin Releasing Hormone (GnRH) on folliculogenesis in the domestic pigeon, Columba livia.

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Asian J. Exp. Sci., Vol. 22, No. 3, 2008; 439-443 Effect of Gonadotrophins and Gonadotrophin Releasing Hormone (GnRH) on folliculogenesis in the domestic pigeon, Columba livia. V. D. Hegde Department of Zoology, Karnatak university, Dharwad - 580 003 (Karnataka); India Abstracts : Effect of Gonadotraphon FSH (5 IU/day/D.Water/10 injections and 10 IU /day/ D.Water/10 injections) Gonadotraphon L H (5 IU/day/D.Water/10 injections) and GnRH (50 ng/day/d.water/10 injections) on folliculogenesis in 5 day hatchlings of the domestic pigeon Columba livia was investigated. The ovaries in initial control (5 day old Hatchlings) contained only oocytes but not primordial follicles. The of the follicles present in other groups were measured and classified. Follicles above 75 µm appeared in 5 IU Gonadotraphon FSH treated, 10 IU Gonadotraphon FSH treated and GnRH treated birds. The follicles above 125 µm were found only in 10 IU Gonadotraphon FSH treated birds. Also, there was a significant increase in the of the largest follicle of 10 IU Gonadotraphon FSH treated group when compared to that in final control group. The present study suggests that in C. livia gonadotrophins may not be required for folliculogenesis. Key word : Gonadotrophins, GnRH, Folliculogenesis, Columba livia Introduction Patterns of oogonial proliferation, oogenesis and folliculogenesis are described in some species of vertebrates (Gondos, 1978; Peters, 1978; Tokarz, 1978 ; Licht 1984; Guraya 1989; Saidapur, 1989; Byskov and Hoyer, 1994). Later study by Motta et al (1995) on lizard Podarcis sicula suggested that FSH in addition to regulating oogonial proliferation and oogenesis it also influenced folliculogenesis. The process of folliculogenesis (formation of primordial follicles) is similar in all vertebrates. There is no definite information on the endocrine events, if any, controlling folliculogenesis in teleosts. In amphibians (anurans) available reports suggest that early primary follicular growth is independent of hormonal regulation (Saidapur, 1989). On the other hand, some studies on reptiles point out that follicle stimulating hormone (FSH) is needed for the growth of primary follicle (Jones et al., 1975, 1976) while others suggest that early follicular growth is gonadotrophin independent (Eyeson, 1971; Ortiz and Marales, 1974). To the best of our knowledge, nothing is known about the hormonal regulation of folliculogenesis in birds. The present study was undertaken to find out the effect of gonadotrophins (Gonadotraphon-FSH and gonadotraphon-lh) and GnRH on the folliculogenesis in newly hatched domestic pigeon, Columba livia. Material and Methods Five day old female hatchlings were selected from the pigeon colony maintained in the Zoology Department, Karnatak University, Dharwad, India. A group of five hatchlings was autopsied on the day of commencement of the experiment to serve as the initial control. At autopsy, weight of the body and that of the left ovaries were taken * Corresponding author : V.D. Hegde, Zoological Survey of India, M-Block, New Alipore, Kolkata - 700 053; India; E-mail : hegde67@yahoo.co.in 439

Hegde V.D. (2008) Asian J. Exp. Sci., 22(3), 439-443 and fixed in Bouin s fluid. (Since there is no sexual dimorphism in hatchlings of pigeon, the number of hatchlings used in each group was more and at autopsy, only the female hatchlings were taken for further analysis). The remaining hatchlings were divided intyo five groups (5 hatchlings/group) and treatment protocol was as follows: Group 1 - Final control - 0.1 ml of distilled water. Group 2 - LH treated - 5 IU of gonadotraphon LH (Batch No. 782007/1 Paines and Byrne Ltd., England). Group 3 - FSH treated - 5 IU of gonadotraphon FSH (Batch No. 720052, Paines and Byrne Ltd.,England) Group 4 - FSH treated -10 IU of gonadotraphon FSH (Batch No. 720052, Paines and Byrne Ltd.,England) Group 5 - GnRH treated - 50 ng of GnRH / 0.1 ml distilled water. (LH-FSH-RH (Chloride form) Batch No. 2 NIAMDD, NIH, Bethesda, Maryland). Since avian gonadotrophins are not commercially available the mammalian gonadotrophins were used. All the injections were made through the intramuscular route in the wing web every alternate day till day 23 after hatching (total 10 injections per bird). The hatchlings were autopsied a day after the last injection. At autopsy, the weight of the body and that of the ovary was recorded. The ovaries were fixed in Bouin s fluid and processed for histological studies. 5 µm thick serial sections were cut and stained with Harris haematoxylin and eosin. The following histometric data were collected from these sections. 1. The number of normal and atretic follicles was counted from every 10th section of each ovary and the mean number of normal and atretic follicles for each groups was calculated. 2. The follicles were classified into four groups based on their : (i) Follicles less than 25 µm. (ii) Follicles between 26 µm to 50 µm. (iii) Follicles between 51 µm to 75 µm. (iv) Follicles greater than 75 µm. 3. Diameters of 15 largest follicles were recorded using an ocular micrometer from each bird in every group and the mean of largest follicular for every group was calculated. The data obtained were analysed by Kruskal-Wallis one way of analysis of variance followed by Scheffe simultaneous confidence interval test (Miller, 1981). Results There was no significant change in the weight of the ovary in different groups. The ovaries of initial controls contained oocytes and no primordial follicles. In all treatment groups, the ovaries contained follicles of different sizes. Some follicles were also seen to undergo atresia in all the groups. The ovaries in 5 IU gonadotrophin LH treated group were similar to that present in the final control. There was no significant change in either the total number of follicles or the of the largest follicle in LH-treated group when compared to that in final controls. (Table A). In both the final control and LH-treated groups, follicles above 75 µ m were not found. In 5 IU and 10 IU gonadotraphon-fsh and GnRH treated groups, follicles above 75 µm appeared whereas in the group treated with 10 IU gonadotraphon-fsh, the follicles ranged up to 120 µm. and there was a significant increase in of the largest follicles when compared to that in the final control group (Table 1). However, there was 440

Effect of Gonadotrophins and Gonadotrophin Releasing Hormone (GnRH) on folliculogenesis in the domestic pigeon, Columba livia. no significant change in the total number of follicles in Gonadotraphon-FSH and GnRH treated birds when compared to that in the final control (Table 1). Discussion The fecundity of females of each vertebrate species is primarily determined by the number of oogonia produced, their differentiation in to primary oocyte and the number of primordial follicles produced by the ovary (Tokarz, 1978). Consequently, a number of studies on mammals and some nonmammalian vertebrates were directed to understand the endocrine mechanism (if any) controlling the oogonial proliferation, oogenesis and folliculogenesis. There is sufficient evidence suggesting that the early follicular development is influenced by gonadotrophins in mammals (Greenwald and Terranova, 1988; Byskov and hoyer, 1994). In nonmammalian vertebrates whether early follicular growth is gonadotrophin dependent or not, is not resolved with certainity. In immature intact and adult hypophysectomised lizard Anolis. Carolinensis and Podarcis sicula mammalian FSH increased the number of primordial follicles (Jones et al., 1975, 1976; Motta et al, 1995). On the otherhand, in lizard Agama agama early follicular growth is shown to be gonadotrophin independent (Eyeson, 1971; Ortiz and Marales, 1974). In anuran amphibians early follicular growth is considered to be gonadotrophin independent (Tokarz, 1978; Saidapur, 1989). To the best of our knowledge, the present study is the first report on the effect of gonadotrophins and GnRH on the follicular growth in newly hatched birds. Since there was no significant change in the number of follicles below 25 µm and the total number of follicles in gonadotraphon-lh, gonadotraphon- FSH and GnRH treated birds, it seems that folliculogenesis is independent of gonadotrophins in Columba livia. However, the appearance of follicles above 75 µm in gonadotraphon-fsh treated hatchlings suggest that FSH has a stimulatory role in follicular growth. GnRH treated birds also had follicles above 75 µm. Since, in the present study, gonadotraphon-lh had no stimulatory role in the growth of the follicles, the stimulatory effect of GnRH on follicular growth seems to be due to its action via FSH of bird s own pituitary. The present study infers that FSH type of gonadotrophin is needed for growth of the follicles, whereas folliculogenesis may not be dependent on gonadotrophins in C. livia. Acknowledgements Author thanks Prof. B.A. Shanbhag, F.A.Sc., F.N.A. Department of Zoology, Karnatak University, Dharwad under whose guidance this work was carried out and supported by UGC grant No: F-3/88/90-SR II sanctioned to Dr. B.A. Shanbhag. Thanks are also due to Director-in-Charge, Zoological Survey of India, for granting the permission to publish this paper. 441

Hegde V.D. (2008) Asian J. Exp. Sci., 22(3), 439-443 Table 1 :Effect of Gonadotraphon -LH, Gonadotraphon-FSH and GnRH on the ovary with respect to number of different size normal follicles and the mean (µm) of the largest follicles in hatchlings of the pigeon, Columba livia. Control (Dist. Water Treated 0.1 ml./alternate Gonadotraphon-LH Treated (5 IU/Alternate Groups Gonadotraphon-FSH Treated (5 IU/Alternate Gonadotraphon-FSH Treated (10 IU/Alternate GnRH Treated (50 ng/alternate <0.25 µm 3130.20 546.07 4038.40 716.90 3745.80 257.80 4098.00 401.00 4028.00 702.60 Number of follicles S.E. 0.26-0.50 µm 1289.80 217.00 1024.60 186.20 1151.00 130.70 1319.20 238.30 1101.00 201.80 0.51-0.76 µm 727.00 152.60 551.40 113.90 462.20 69.30 822.20 113.10 879.60 122.20 >0.76 µm - - 138.20 16.30 653.20 77.20 721.40 39.00 Total No. of Normal follicles 5147.00 784.90 5614.00 390.60 5498.00 175.50 6251.00 600.30 6700.00 800.20 Total No.l of Atretic follicles 702.80 110.10 863.00 51.80 632.20 29.80 774.20 136.60 621.60 28.00 Mean Diameter of largest follicle (µm) 76.65 2.40 66.80 4.40 86.70 1.90 120.30 11.00 93.30 5.80 1. Total number of injections ten. 2. Figures superscribed by the same alphabets are statistically significant at 0.05 level. 442

Effect of Gonadotrophins and Gonadotrophin Releasing Hormone (GnRH) on folliculogenesis in the domestic pigeon, Columba livia. References Byskov A.G. and Hoyer P.E. (1994) : Embryology of mammalian gonads and ducts. In : The physiology of Reproduction (E. Knobil and J.D. Neill, eds.), Raven Press, New York, pp. 487-539. Eyeson K.N. (1971) : Pituitary control of ovarian activity in the lizard, Agama agama. J. Zool., 165, 367-372. Gondos B. (1978) : Oogonia and oocytes in mammals. In : The Vertebrate Ovary : Comparative Biology and Evolution. (R.E. Jones, ed), Plenum Press, New York and London, pp. 83-113. Greenwald G..S. and Terranova P. F. (1988) : Follicular selection and its control. In: The physiology of Reproduction (E. Knobil and J. Neill et al., eds.) Raven Press, New York, pp. 387-445. Guraya S.S. (1989) : Ovarian follicles in reptiles and birds. Zoophysiology, vol.24, Springer Verlag, Berlin, Heidelberg, NewYork. Jones R.E., Tokarz R.R. and La Greek F.T. (1975): Endocrine control of clutch size in reptiles. V: FSH-induced follicular formation and growth in immature ovaries of Anolis carolinensis. Gen. Comp. Endocrinol., 26, 354-367. Jones R.E., Tokarz R.R. and La Greek F.T. and Fitzgerald K.T. (1976) : Endocrine control of clutch size in reptiles. VI : Patterns of FSHinduced ovarian stimulation in adult Anolis carolinensis. Gen. Comp. Endocrinol., 30, 101-116. Licht P. (1984) : Reptiles. In : : Marshall s Physiology of Reproduction, vol. 1 : Reproductive cycles of Vertebrates (G.E. Laming, ed.), 4 th ed. Churchill Livingstone, New York, pp. 206-282. Miller R.G. Jr. (1981) : Simultaneous statistical inference. Springer-Verlag, New York, Heidelberg, Berlin. Motta C.M., Borrelli L. and Filosa S. (1995) : The effects of follicle stimulating hormone treatment on early meiotic oocytes of Podarcis sicula (Lacertilia). Gen. Comp. Endocrinol., 99., 1-5. Ortiz E. and Marales M.H. (1974) : Development and function of the female reproductive tract of the tropical lizard, Anolis pulchellus.physiol. Zool., 47, 207-217. Peters H. (1978) Folliculogenesis in mammals. In:. The Vertebrate Ovary : Comparative Biology and Evolution. (R.E. Jones, ed), Plenum Press, New York and London, pp. 121-140. Saidapur S.K (1989). Reproductive cycles of amphibians. In: Reproductive cycles of Indian Vertebrates (S.K. Saidapur, ed.), Allied Publishers Ltd, New Delhi, pp: 166-224. Tokarz R.R. (1978) : Oogonial proliferation, oogenesis and folliculogenesis in nonmammalian vertebrates. In: The Vertebrate Ovary: Comparative biology and evolution. (R.E. Jones, ed.), Plenum Press, New York, pp: 145-173. 443