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前列腺素合成酶抑制剂对下丘脑前部神经元的作用:体温调节与生物胺

Action of prostaglandin synthetase inhibitors on rostral hypothalamic neurones: thermoregulation and biogenic amines.

作者信息

Jell R M, Sweatman P

出版信息

Can J Physiol Pharmacol. 1976 Apr;54(2):161-6. doi: 10.1139/y76-026.

Abstract

Sensitivity of neurones in the rostral hypothalamus of methoxyflurane anesthetized cats to the prostaglandin synthetase inhibitors (PGSIs), salicylate and fenoprofen, has been examined using the technique of microiontophoresis. Results were compared with sensitivity to prostaglandin (PG) E1 and no noradrenaline (NA) and 5-hydroxytryptamine (5HT). Simultaneous applications of PGSIs and NA or 5HT were made to investigate the role of PG in monoamine induced changes in neuronal excitability. PGSIs did not excite these cells, but depression were common, particularly with fenoprofen. PGE1 did not reverse the depressions. NA and 5HT responses were generally unaffected by simultaneous PGSI application and responsiveness to PGSIs was found to be unrelated to amine sensitivity. The results support the conclusion that PGSIs have a depressant action on neurones in this region, which may not be related to inhibition of prostagladin synthesis, and that the actions of microiontophoretically applied NA and 5HT are not dependent upon PG.

摘要

利用微离子电泳技术,研究了甲氧氟烷麻醉猫的下丘脑前部神经元对前列腺素合成酶抑制剂(PGSIs)、水杨酸盐和非诺洛芬的敏感性。将结果与对前列腺素(PG)E1以及去甲肾上腺素(NA)和5-羟色胺(5HT)的敏感性进行了比较。同时应用PGSIs与NA或5HT,以研究PG在单胺诱导的神经元兴奋性变化中的作用。PGSIs不会使这些细胞兴奋,但抑制作用很常见,尤其是非诺洛芬。PGE1不会逆转这种抑制作用。NA和5HT反应通常不受PGSI同时应用的影响,并且发现对PGSIs的反应性与胺敏感性无关。结果支持以下结论:PGSIs对该区域的神经元有抑制作用,这可能与前列腺素合成的抑制无关,并且微离子电泳应用的NA和5HT的作用不依赖于PG。

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