Srivastava Vinod K, Hiney Jill K, Stevener Kristyn, Dees William L
Department of Veterinary Integrative Biosciences, College of Veterinary Medicine, Texas A&M University, College Station, Texas.
Alcohol Clin Exp Res. 2015 Dec;39(12):2386-93. doi: 10.1111/acer.12905. Epub 2015 Nov 26.
An increase in development of excitatory inputs along with a decline in inhibitory inputs ultimately govern the timely increased secretion of hypothalamic luteinizing hormone-releasing hormone (LHRH) at the time of puberty. As chronic alcohol (ALC) exposure acts at the hypothalamic level to suppress LHRH secretion and delay puberty, we assessed its ability to differentially affect the expression of key puberty-related proteins.
ALC was administered to female rats from days 27 to 33, at which time animals were killed and tissues collected for protein expression. In the medial basal hypothalamus (MBH), we assessed kisspeptin (Kp) 10, an excitatory peptide critical for prepubertal LHRH secretion, and Lin28b, a peptide with an inhibitory influence on puberty. As a direct mechanism of action of Lin28b was not known, we determined whether its central administration could induce dynorphin (DYN), a peptide that is inhibitory on LHRH secretion. Also, ALC's effect on DYN protein expression was assessed, as well as its effect on DYN release in vitro.
ALC markedly suppressed (p < 0.01) the expression of the excitatory Kp protein, while at the same time increased (p < 0.001) the expression of inhibitory Lin28b protein. Subsequently, we showed for the first time that the central administration of Lin28b stimulated (p < 0.01) the synthesis of DYN. Finally, ALC also induced (p < 0.01) the protein expression and stimulated (p < 0.01) the in vitro release of DYN from the MBH.
These results indicate that ALC can simultaneously and differentially alter both excitatory and inhibitory influences governing pubertal development, show for the first time a mechanism of action by which Lin28b exerts its prepubertal inhibitory tone, and further demonstrate the negative influences of ALC on the pubertal process.
青春期时,兴奋性输入的增加以及抑制性输入的减少最终控制下丘脑促黄体生成激素释放激素(LHRH)分泌的适时增加。由于长期酒精(ALC)暴露作用于下丘脑水平以抑制LHRH分泌并延迟青春期,我们评估了其对关键青春期相关蛋白表达的差异性影响能力。
从第27天至第33天对雌性大鼠给予ALC,此时处死动物并收集组织用于蛋白表达分析。在内侧基底下丘脑(MBH)中,我们评估了对青春期前LHRH分泌至关重要的兴奋性肽亲吻素(Kp)10,以及对青春期有抑制作用的肽Lin28b。由于Lin28b的直接作用机制尚不清楚,我们确定其脑内给药是否能诱导强啡肽(DYN),一种对LHRH分泌有抑制作用的肽。此外,评估了ALC对DYN蛋白表达的影响及其对体外DYN释放的影响。
ALC显著抑制(p < 0.01)兴奋性Kp蛋白的表达,同时增加(p < 0.001)抑制性Lin28b蛋白的表达。随后,我们首次表明脑内给予Lin28b刺激(p < 0.01)DYN的合成。最后,ALC还诱导(p < 0.01)MBH中DYN的蛋白表达并刺激(p < 0.01)其体外释放。
这些结果表明,ALC可同时且差异性地改变控制青春期发育的兴奋性和抑制性影响,首次展示了Lin28b发挥青春期前抑制作用的作用机制,并进一步证明了ALC对青春期进程的负面影响。