Effects of Cabergoline on Embryo Growth: Macroscopic and Molecular Findings

Gholamhossien Darya1, Javad Moayedi2, Zeinab Dehghan1,3

  • 11Department of Comparative Biomedical Sciences, School of Advanced Medical Sciences and Technologies, Shiraz University of Medical Sciences, Shiraz, Iran.

PubMed
Abstract

Insights

Cabergine (CAB) impacts prolactin (PRL) levels and fetal development in chickens. This study investigated CAB

Area of Science:

  • Endocrinology
  • Developmental Biology
  • Pharmacology

Background:

  • Prolactin (PRL) is a key neurohypophyseal hormone influencing behavior, growth, and angiogenesis.
  • Cabergine (CAB) is known to suppress PRL effects by targeting the dopamine D2 receptor (D2R).

Purpose of the Study:

  • To investigate the potential side effects of Cabergine (CAB) on fetal development.
  • To examine the impact of CAB on prolactin (PRL) gene expression and related physiological parameters in a chicken model.

Main Methods:

  • Utilized in silico and in vivo approaches with 30 fertilized chicken eggs divided into control and two CAB-treated groups (0.5 mg/kg and 1 mg/kg).
  • Analyzed embryo weight, body length, chorioallantoic vessel length, and relative PRL gene expression after 18 days.
  • Employed the STRING database for in silico analysis of prolactin-protein interactions and functional pathways.

Main Results:

  • CAB treatment at 0.5 mg/kg increased embryo weight, while 1 mg/kg decreased it compared to controls.
  • A significant reduction in body size and increased chorionic vessel development were noted at 0.5 mg/kg CAB.
  • PRL gene expression significantly decreased in both CAB-treated groups.
  • In silico analysis identified conserved interactions between PRL, INS, and POMC proteins in humans and chickens.

Conclusions:

  • Cabergine (CAB) effectively reduces prolactin (PRL) levels in developing chicken embryos.
  • CAB administration influences fetal weight and body size, indicating potential developmental side effects.
  • Identified conserved protein interactions relevant to PRL function across species.