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反射性内脏神经刺激可增加大鼠肾上腺髓质中前脑啡肽原A mRNA和前脑啡肽原A相关肽的水平。

Reflex splanchnic nerve stimulation increases levels of proenkephalin A mRNA and proenkephalin A-related peptides in the rat adrenal medulla.

作者信息

Kanamatsu T, Unsworth C D, Diliberto E J, Viveros O H, Hong J S

出版信息

Proc Natl Acad Sci U S A. 1986 Dec;83(23):9245-9. doi: 10.1073/pnas.83.23.9245.

Abstract

The effect of reflex splanchnic nerve stimulation on proenkephalin A biosynthesis was investigated in the rat adrenal medulla. Tissue levels of native [Met5]enkephalin-like immunoreactivity (IR) (measured by direct RIA of tissue extracts), cryptic [Met5]enkephalin-like IR (calculated as the increase in [Met5]enkephalin-like IR detected in tissue extracts after sequential digestion with trypsin and carboxypeptidase B), and proenkephalin A mRNA were determined in adrenal medulla from rats sacrificed at various times after a period of insulin-induced hypoglycemia. Two hours of insulin hypoglycemia, which produced intense reflex stimulation of the splanchnic nerves as evidenced by a 55% decrease in the adrenal medulla catecholamine levels, resulted in a 3-fold increase in proenkephalin A mRNA levels in this tissue. The proenkephalin A mRNA levels reached a maximum 15-fold increase over control values 24 hr after this period of hypoglycemic stress and then gradually declined with an approximate half-life of 4 days. Native and cryptic [Met5]enkephalin-like IR had increased 9-fold and 12-fold, respectively, 24 hr after this period of hypoglycemia, and both demonstrated maximum increases of 130-fold and 50-fold, respectively, after 96 hr. Combined pretreatment (i.p. administration) with the ganglionic and muscarinic blocking agents chlorisondamine (5 mg/kg of body weight) and atropine (1 mg/kg) blocked the increase in levels of proenkephalin A mRNA seen in the rat adrenal medulla following insulin hypoglycemia. These data indicate that reflex splanchnic nerve discharge stimulates proenkephalin biosynthesis, probably at the level of gene expression.

摘要

在大鼠肾上腺髓质中研究了反射性内脏神经刺激对前脑啡肽原A生物合成的影响。测定了胰岛素诱导低血糖一段时间后不同时间处死的大鼠肾上腺髓质中天然[Met5]脑啡肽样免疫反应性(IR)(通过组织提取物的直接放射免疫分析测定)、隐蔽性[Met5]脑啡肽样IR(计算为用胰蛋白酶和羧肽酶B顺序消化后组织提取物中检测到的[Met5]脑啡肽样IR的增加量)以及前脑啡肽原A mRNA的组织水平。两小时的胰岛素低血糖导致肾上腺髓质儿茶酚胺水平降低55%,这表明产生了强烈的内脏神经反射性刺激,该低血糖期后此组织中的前脑啡肽原A mRNA水平增加了3倍。在这段低血糖应激期后24小时,前脑啡肽原A mRNA水平比对照值增加了15倍达到最大值,然后逐渐下降,半衰期约为4天。在此低血糖期后24小时,天然和隐蔽性[Met5]脑啡肽样IR分别增加了9倍和12倍,96小时后两者分别显示出最大增加量130倍和50倍。用神经节阻断剂和毒蕈碱阻断剂氯异吲哚铵(5毫克/千克体重)和阿托品(1毫克/千克)联合预处理(腹腔注射)可阻断胰岛素低血糖后大鼠肾上腺髓质中前脑啡肽原A mRNA水平的增加。这些数据表明反射性内脏神经放电刺激前脑啡肽原的生物合成,可能是在基因表达水平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb7c/387112/b380a12c2bda/pnas00327-0435-a.jpg

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