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Obesity is now dramatically on the rise and is a major risk factor for diabetes. Besides primary metabolic health problems occurring in people with obesity and diabetes there are numerous secondary problems including disruptions of the reproductive system. Kisspeptins and its receptor GPR54 play a key role in regulation of reproduction and integration of metabolic and reproductive systems. We hypothesized that obese and/or diabetic male rats would have altered Kiss-1 and/or GPR54 mRNA levels in the hypothalamic-pituitary-gonadal (HPG) axis. Rats were fed with high fat diet (HFD) for 5 weeks to induce obesity (DIO group). Injections of STZ were performed to induce diabetes type 1 (STZ group) or diabetes type 2 (HFD/STZ group). Control animals (C group) were fed with lab chow diet. Real-time PCR was performed. We have found that: (1) Kiss-1 and GPR54 expression in HPG axis was related to the rat metabolic status; (2) both STZ and HFD/STZ rats had elevated GPR54 mRNA level in the hypothalamus and (3) STZ rats had decreased Kiss-1 mRNA levels in the pituitary and decreased GPR54 levels in the testis. We have concluded that observed changes may contribute to reproductive failure in animals with diabetes. Supported by grant NCN 2011/01/B/NZ4/04992.
INTRODUCTION: Kisspeptin (KP) is involved in multiple hypothalamic regulatory processes such as estrogenic feedback to GnRH neurons via synaptic connections. We have reported previously that GnRH neurons send endocannabinoid retrograde signals to regulate their GABAergic input. KP‑producing neurons co‑synthesize GABA or glutamate both in the preoptic (POA) and arcuate (ARC) subpopulations. Moreover, we found the cannabinoid receptor type one (CB1) mRNA in these areas. However, it is unknown whether any subpopulation of KP neurons is under the influence of endocannabinoids. AIM(S): 1) To identify the GABAergic and glutamatergic subpopulations of KP neurons in female mice. 2) To determinate whether CB1 transcripts can be detected in any of the subpopulation of POA or ARC KP neurons. METHOD(S): The transcripts of KP, CB1, and the GABAergic and glutamatergic marker proteins, i.e., vesicular inhibitory amino acid transporter (VIAAT), and vesicular glutamate transporter-2 (VGLUT2) have been detected by RNAscope in situ hybridization technique. The signal was analyzed by confocal microscopy and quantified using our in‑house developed program. RESULTS: We found a significantly increased KP mRNA expression in the POA of ovariectomised mice after estradiol replacement. CB1 mRNAs were found in GABAergic and glutamatergic KP neurons of the POA and ARC. About 67% (AVPV) – 43% (ARC) of the GABAergic KP neurons expressed CB1 mRNA in the OVX+OIL mice, and about 31% (AVPV) – 36% (ARC) of the GABAergic KP neurons expressed CB1 mRNA in the OVX+EB mice. Concerning the glutamatergic KP neurons, about 19% (AVPV) ‑14% (ARC) expressed CB1 mRNA in the OVX- +OIL mice and about 24% (AVPV) – 43% (ARC) of them expressed CB1 mRNA in the OVX+EB mice. CONCLUSIONS: The hormonal status of mice influences the number of KP neurons expressing CB1 and endocannabinoids likely regulate the electrical activity of different KP subpopulations involved in the regulation of various hypothalamic processes.
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