Gill-Sharma M K, Aleem M, Sethi G, Choudhary J, Padwal V, D'Souza S, Balasinor N, Parte P, Juneja H S
Department of Neuroendocrinology, National Institute for Research in Reproductive Health (ICMR), Parel, Mumbai, India.
J Endocrinol Invest. 2003 Apr;26(4):316-26. doi: 10.1007/BF03345179.
The underlying mechanisms in human infertility associated with hyperprolactinemia have yet to be established. Hyperprolactinemia is a known side-effect of fluphenazine, a broad spectrum, long-acting phenothiazine known to be D2 dopamine receptor antagonist. Dose-related effects of fluphenazine decanoate were ascertained on the fertility of 60-day treated, adult male rats. Significant increase in the serum levels of prolactin and decrease in the levels of LH and FSH were seen at doses of 1-3 mg/kg/day. No effect was evident on the serum testosterone (T) and estradiol. The tissue levels of Inhibins were not affected. The weights of testes, epididymides, seminal vesicles, ventral prostate, adrenal and pituitary glands were not affected. Testicular histology showed sloughing indicating the sensitivity of this parameter to FSH deficiency. Mating occurred within 10 days of cohabitation in the control and 1-2 mg/kg/day treated groups but delayed in the 3 mg/kg/day treated group with a significant effect on potency. Implantation sites, litter size and fertility index were significantly reduced at 2-3 mg/kg/day doses of fluphenazine. No effects however were seen on sperm counts or motility whereas morphological changes were apparent in the acrosome. Chromatin decondensation in vitro was enhanced and sperm chromatin structure assay revealed DNA denaturation. Hypothalamic tyrosine hydroxylase levels were increased in 1-3 mg/kg/day dose range. Hyperprolactinemic males sired fewer pups as compared to controls. Hypothalamic tyrosine hydroxylase was upregulated at all the doses. The antifertility effects of fluphenazine-induced hyperprolactinemia appeared to be unrelated to testosterone (T). In addition, FSH decrease might have affected the intrinsic sperm quality and thereby reduced litter size.
与高催乳素血症相关的人类不孕的潜在机制尚未明确。高催乳素血症是氟奋乃静已知的副作用,氟奋乃静是一种广谱、长效的吩噻嗪类药物,已知是D2多巴胺受体拮抗剂。研究了癸酸氟奋乃静对经60天治疗的成年雄性大鼠生育力的剂量相关影响。在剂量为1 - 3毫克/千克/天时,血清催乳素水平显著升高,促黄体生成素(LH)和促卵泡生成素(FSH)水平降低。血清睾酮(T)和雌二醇水平未受明显影响。抑制素的组织水平未受影响。睾丸、附睾、精囊、腹侧前列腺、肾上腺和垂体的重量未受影响。睾丸组织学显示有脱落现象,表明该参数对FSH缺乏敏感。对照组和1 - 2毫克/千克/天治疗组在同居10天内发生交配,但3毫克/千克/天治疗组交配延迟,对生育能力有显著影响。在2 - 3毫克/千克/天的氟奋乃静剂量下,着床部位、窝仔数和生育指数显著降低。然而,对精子数量或活力没有影响,而顶体出现明显的形态变化。体外染色质解聚增强,精子染色质结构分析显示DNA变性。在1 - 3毫克/千克/天剂量范围内,下丘脑酪氨酸羟化酶水平升高。与对照组相比,高催乳素血症雄性大鼠的幼崽数量较少。所有剂量下下丘脑酪氨酸羟化酶均上调。氟奋乃静诱导的高催乳素血症的抗生育作用似乎与睾酮(T)无关。此外,FSH降低可能影响了精子的内在质量,从而减少了窝仔数。