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外周乙酰胆碱酯酶抑制剂,新斯的明,可防止发情周期卵泡期炎症依赖性 GnRH/LH 分泌抑制。

Peripheral Inhibitor of AChE, Neostigmine, Prevents the Inflammatory Dependent Suppression of GnRH/LH Secretion during the Follicular Phase of the Estrous Cycle.

机构信息

The Kielanowski Institute of Animal Physiology and Nutrition, Polish Academy of Sciences, Jabłonna, Poland.

Institute of Animal Reproduction and Food Research, Polish Academy of Sciences, Olsztyn, Poland.

出版信息

Biomed Res Int. 2017;2017:6823209. doi: 10.1155/2017/6823209. Epub 2017 Aug 15.

DOI:10.1155/2017/6823209
PMID:28894751
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5574266/
Abstract

The study was designed to test the hypothesis that the inhibition of acetylcholinesterase (AChE) activity at the periphery by Neostigmine (0.5 mg/animal) will be sufficient to prevent inflammatory dependent suppression of the gonadotropin-releasing hormone (GnRH)/luteinising hormone (LH) secretion in ewes in the follicular phase of the estrous cycle, and this effect will be comparable with the systemic AChE inhibitor, Donepezil (2.5 mg/animal). An immune/inflammatory challenge was induced by peripheral administration of lipopolysaccharide (LPS; 400 ng/kg). Peripheral treatment with Donepezil and Neostigmine prevented the LPS-induced decrease ( < 0.05) in LH gene expression in the anterior pituitary gland (AP) and in LH release. Moreover, Donepezil completely abolished ( < 0.05) the suppressory effect of inflammation on GnRH synthesis in the preoptic area, when pretreatment with Neostigmine reduced ( < 0.05) the decrease in GnRH content in this hypothalamic structure. Moreover, administration of both AChE inhibitors diminished ( < 0.05) the inhibitory effect of LPS treatment on the expression of GnRH receptor in the AP. Our study shows that inflammatory dependent changes in the GnRH/LH secretion may be eliminated or reduced by AChE inhibitors suppressing inflammatory reaction only at the periphery such as Neostigmine, without the need for interfering in the central nervous system.

摘要

这项研究旨在检验以下假设

外周乙酰胆碱酯酶(AChE)抑制剂新斯的明(0.5mg/动物)的抑制作用足以防止发情周期卵泡期母羊中促性腺激素释放激素(GnRH)/黄体生成素(LH)分泌的炎症依赖性抑制,并且这种作用与全身乙酰胆碱酯酶抑制剂多奈哌齐(2.5mg/动物)相当。通过外周给予脂多糖(LPS;400ng/kg)诱导免疫/炎症挑战。外周给予多奈哌齐和新斯的明可防止 LPS 诱导的前垂体(AP)LH 基因表达和 LH 释放减少(<0.05)。此外,当用新斯的明预处理时,炎症对下丘脑前区 GnRH 合成的抑制作用完全被消除(<0.05),而新斯的明减少了该下丘脑结构中 GnRH 含量的减少(<0.05)。此外,两种 AChE 抑制剂的给药均减少(<0.05)了 LPS 处理对 AP 中 GnRH 受体表达的抑制作用。我们的研究表明,仅通过抑制外周炎症反应(如新斯的明),而无需干扰中枢神经系统,就可以消除或减少 AChE 抑制剂对 GnRH/LH 分泌的炎症依赖性变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35a9/5574266/a6dcc870b7c2/BMRI2017-6823209.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35a9/5574266/ecfc9c97bb61/BMRI2017-6823209.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35a9/5574266/1494aa23b089/BMRI2017-6823209.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35a9/5574266/146e513a1109/BMRI2017-6823209.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35a9/5574266/a6dcc870b7c2/BMRI2017-6823209.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35a9/5574266/ecfc9c97bb61/BMRI2017-6823209.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35a9/5574266/1494aa23b089/BMRI2017-6823209.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35a9/5574266/146e513a1109/BMRI2017-6823209.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35a9/5574266/a6dcc870b7c2/BMRI2017-6823209.004.jpg

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