Mahmoodzadeh Sagheb Mandana, Azarpira Negar, Yaghobi Ramin
Department of Biology, Kazeroon Branch, Islamic Azad University, Kazeroon, IR Iran.
Transplant Research Center, Shiraz University of Medical Sciences, Shiraz, IR Iran.
Int J Endocrinol Metab. 2014 Apr 1;12(2):e15297. doi: 10.5812/ijem.15297. eCollection 2014 Apr.
Leptin and adiponectin are the two key metabolic hormones secreted from adipocytes to control food intake and energy expenditure. The action of both hormones in regulation of Gonadotropin Releasing Hormone (GnRH) secretion from the hypothalamus is mediated through Kisspeptins. Kisspeptins are products of KiSS-1 gene. Leptin and adiponectin are modulators of KiSS-1 expression in the hypothalamus. These peptides have also important roles in pancreatic β-cells to control insulin synthesis and secretion and their receptors are detected in Langerhans islets. We hypothesized that leptin and adiponectin might alter KiSS-1 and Kiss Receptor mRNA expression in the islets.
The aim of this study is to investigate any modulatory effect that leptin and adiponectin may have on the expression of Kiss-1 and KiSSR gene in Langerhans islets.
We isolated the islets from adult male rats by collagenase and cultured CRI-D2 cell lines to investigate the effect of leptin and adiponectin. Then, we incubated them with different concentrations of leptin and adiponectin for 24 hours. After that, RNA was extracted from the islets and CRI-D2 cells and transcripted to cDNA. KiSS-1 and KissR expression levels were evaluated by real time PCR.
In islet and CRI-D2 cells, leptin increased the KiSS-1 mRNA expression significantly, but adiponectin decreased it was expected.
These findings indicated the possibility that KiSS-1 mRNA expression is a mediator of leptin and adiponectin function in the islets.
瘦素和脂联素是脂肪细胞分泌的两种关键代谢激素,用于控制食物摄入和能量消耗。这两种激素在下丘脑调节促性腺激素释放激素(GnRH)分泌的作用是通过亲吻素介导的。亲吻素是KiSS-1基因的产物。瘦素和脂联素是下丘脑KiSS-1表达的调节因子。这些肽在胰腺β细胞中对控制胰岛素合成和分泌也具有重要作用,并且在胰岛中可检测到它们的受体。我们推测瘦素和脂联素可能会改变胰岛中KiSS-1和亲吻受体mRNA的表达。
本研究的目的是调查瘦素和脂联素对胰岛中Kiss-1和KiSSR基因表达可能产生的任何调节作用。
我们通过胶原酶从成年雄性大鼠中分离出胰岛,并培养CRI-D2细胞系以研究瘦素和脂联素的作用。然后,我们将它们与不同浓度的瘦素和脂联素孵育24小时。之后,从胰岛和CRI-D2细胞中提取RNA并转录为cDNA。通过实时PCR评估KiSS-1和KissR的表达水平。
在胰岛和CRI-D2细胞中,瘦素显著增加了KiSS-1 mRNA的表达,但脂联素如预期的那样降低了其表达。
这些发现表明KiSS-1 mRNA表达可能是瘦素和脂联素在胰岛中发挥功能的介质。