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.

Download full-text PDF

Source
http://dx.doi.org/10.1007/BF03345179DOI Listing

Publication Analysis

Top Keywords

antifertility effects
8
effects fluphenazine
8
adult male
8
male rats
8
1-3 mg/kg/day
8
mg/kg/day treated
8
litter size
8
hypothalamic tyrosine
8
tyrosine hydroxylase
8
mg/kg/day
5

Similar Publications

Responses in organs, sperm, steroid hormones and CYP450 enzyme in male mice treated by quinestrol only or in conjunction with clarithromycin.

Sci Rep

November 2024

Guangdong Key Laboratory of Animal Conservation and Resource Utilization, Guangdong Public Laboratory of Wild Animal Conservation and Utilization, Institute of Zoology, Guangdong Academy of Sciences, Guangzhou, China.

Pest rodents persistently undermine crop yields and food security. Fertility control could be a viable alternative for managing rodent populations. This study investigates the antifertility effects of various concentrations of clarithromycin combined with 1.

View Article and Find Full Text PDF

Clinical trials of intratesticular administration of nanostructured lipid carriers encapsulated alpha-mangostin: Safety and efficacy on feline reproductive health.

Theriogenology

January 2025

Department of Obstetrics, Gynaecology and Reproduction, Faculty of Veterinary Science, Chulalongkorn University, 39 Henri-Dunant Rd., Pathumwan, Bangkok, 10330 Thailand. Electronic address:

Surgical castration is a primary method for controlling male fertility, but it is impractical for large-scale population control of stray animals. Developing nanoparticle-mediated sterilants that induce cell apoptosis rather than necrosis is a complex and promising area of research. This study aimed to investigate the impact of intratesticular administration of alpha-mangostin encapsulated in nanostructured lipid carriers (AM-NLC) on testicular changes and any associated adverse effects over a 168-day observation period.

View Article and Find Full Text PDF

Objective: Gossypol is a natural polyphenolic dialdehyde product that is primarily isolated from cottonseed. It is a racemized mixture of (-)-gossypol and (+)-gossypol that has anti-infection, antimalarial, antiviral, antifertility, antitumor and antioxidant activities, among others. Gossypol optical isomers have been reported to differ in their biological activities and toxic effects.

View Article and Find Full Text PDF
Article Synopsis
  • Triptolide is a bioactive compound with strong anti-inflammatory, immunosuppressive, antifertility, and anticancer properties but has limited clinical use due to poor water solubility and significant toxicity (especially to the liver, kidneys, and heart).
  • Its therapeutic and toxic effects arise from its action on the XPB protein, which is critical for DNA processes, leading to reduced transcription and DNA repair.
  • Recent advancements like triptolide prodrugs and derivatives aim to improve its effectiveness and safety, as this review examines its structure, uses, toxic effects, and interactions to guide future treatments.
View Article and Find Full Text PDF
Article Synopsis
  • The study aimed to investigate the molecular docking characteristics and antifertility effects of extracts derived from PO leaves, specifically petroleum ether and chloroform extracts.
  • Using molecular docking software and animal models, researchers found that the petroleum ether extract (PEEPO) had a stronger anti-implantation effect than the chloroform extract (CHEPO) at various doses.
  • The results suggested that both extracts are safe at high dosages, increase blood estrogen levels, and interact favorably with estrogen receptors, indicating their potential for developing herbal antifertility treatments.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!