The tilapia, Oreochromis mossambicus, shows a short ovarian cycle of 24-26 days in nonmouthbrooding condition. In this study, the stripped female O. mossambicus were exposed to repeated mild acute stressors such as handling, chasing, frequent netting and low water levels daily for a period of 26 days. The follicular dynamics did not show significant difference during previtellogenic phase (day 12), whereas the mean number of stage IV (vitellogenic) follicles remained significantly lower compared with controls at the end of vitellogenic phase (day 18). The stage V (vitellogenic, preovulatory) follicles were completely absent in contrast to their presence in controls prior to spawning (day 23). The control fish spawned spontaneously after 24 days and entered mouthbrooding phase, whereas those exposed to stressors did not spawn. Furthermore, the serum levels of estradiol (E(2)) remained significantly lower concomitant with a significant increase in the serum cortisol concentration during vitellogenic and prespawning phase compared with those of the controls. The LH cells in the PPD of the pituitary gland showed weak immunoreactivity through vitellogenic and prespawning phase in fish exposed to stressors indicating the diminished secretory activity in contrast to the intensely stained ir-material in controls. The study reveals the disruptive effects of aquacultural stressors on the spawning cycle through suppression of LH and E(2) secretion along the pituitary-ovary axis. The results suggest that the ovarian stress response depends on the phase of the cycle and that the interruption of the spawning cycle is due to inhibition of recruitment of preovulatory follicles in O. mossambicus.
Stressors (handling, chasing, and noise) applied randomly five times per day for one month to lizards during the recrudescence phase of the ovarian cycle caused a significant reduction in mean number of oocytes and primordial follicles when compared to those of controls. Further, vitellogenic follicles were absent in the ovary of lizards subjected to stressors. Administration of bovine FSH during post-breeding regression phase of the ovarian cycle induced ovarian recrudescence as shown by significant increases in the mean number of oogonia, oocytes, and primordial follicles compared to controls, as well as vitellogenic growth of follicles. However, lizards treated with FSH and exposed to stressors did not exhibit ovarian recrudescence. Furthermore, FSH administration during the post-breeding regression phase caused a significant increase in serum levels of estradiol compared to controls, which was accompanied by significant increases in the relative weight of the liver and oviduct, as well as vitellogenic growth of follicles. Despite administration of FSH to lizards subjected to stressors, there was neither any increase in serum levels of estradiol and weight of the liver nor vitellogenic growth of follicles. The results indicate that repeated application of stressors inhibits vitellogenic growth of follicles by suppression of steroidogenic activity in M. carinata. This is the first report revealing that the ovary does not respond to gonadotrophin treatment under stressful conditions in reptiles.
In the present study, we examined whether stress-induced suppression of reproduction is mediated through the catecholaminergic neurotransmitter dopamine (DA) in the female cichlid fish Oreochromis mossambicus. In the first experiment, application of antibody against tyrosine hydroxylase (TH; a marker for DA) in brain sections revealed the presence of intensely stained TH immunoreactive cells in the preoptic area (POA) and nucleus preopticus (NPO) during the previtellogenic phase. These cells showed weak immunoreactivity during the vitellogenic and prespawning phases concomitant with darkly stained luteinising hormone (LH) immunoreactive content in the proximal pars distalis (PPD) of the pituitary gland and fully ripened follicles (stage V) in the ovary of control fish. However, in fish exposed to aquacultural stressors, TH secreting cells remained intensely stained in POA and NPO regions during the prespawning phase, indicating increased synthetic and secretory activity, which was reflected by a significantly higher DA content compared to controls. Increased DA activity as a result of stress was associated with a decrease in the LH immunoreactive content in the PPD and an absence of stage V follicles in the ovary. In the second experiment, administration of DA caused effects similar to those in stressed fish, whereas DA receptor antagonist domperidone (DOM) treatment significantly increased the LH content in the PPD and the number of stage V follicles in unstressed fish. On the other hand, treatment of stressed fish with DOM resulted in dark accumulations of LH immunoreactive content in the PPD accompanied by the presence of stage V follicles in the ovary. Taken together, these results suggest an additional pathway for the inhibitory effects of stress through dopaminergic neurones along the reproductive axis.
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