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甘丙肽在大鼠腹侧海马体内刺激N-甲基-D-天冬氨酸受体/一氧化氮/环磷酸鸟苷途径。

Galanin stimulates the N-methyl-D-aspartate receptor/nitric oxide/cyclic GMP pathway in vivo in the rat ventral hippocampus.

作者信息

Consolo S, Uboldi M C, Caltavuturo C, Bartfai T

机构信息

Istituto di Ricerche Farmacologiche Mario Negri, Milan, Italy.

出版信息

Neuroscience. 1998 Aug;85(3):819-26. doi: 10.1016/s0306-4522(97)00586-1.

Abstract

We investigated whether the neuropeptide galanin affects the nitric oxide synthase/cyclic GMP pathway in rat hippocampus by measuring in vivo the extracellular cyclic GMP levels during microdialysis. Galanin (2.5 and 3.5 nmol; i.c.v.) dose-dependently raised the extracellular levels of cyclic GMP in the ventral but not the dorsal hippocampus. The effect of 3.5 nmol galanin was blocked by local application of tetrodotoxin and inhibited by the high-affinity galanin antagonist M40 (galanin-[1-12]-Pro3-[Ala-Leu]2-Ala amide). The non-competitive N-methyl-D-aspartate receptor antagonist dizocilpine maleate (30 microM infused into the ventral hippocampus or 0.2 mg/kg, i.p.) and the competitive one, 3-([R]-carboxypiperazin-4-yl)-propyl-phosphonic acid (50 microM infused), but not local perfusion of the AMPA antagonist 6-nitro-7-sulphamoylbenzo(f)quinoxaline-2,3-dione (15 microM) abolished the galanin-evoked cyclic GMP response in the hippocampus. Inhibitors of nitric oxide synthase, L-Arg(NO2)-OMe.HCl and 7-nitroindazole monosodium salt, applied locally, blocked the galanin-induced increase in hippocampal extracellular cyclic GMP. This increase was also prevented by local application of 1H-(1,2,4)oxadiazolo(4,3a) quinoxalin-1-one, a selective inhibitor of soluble guanylyl cyclase. The galanin receptors mediating the rise in cyclic GMP reside outside the hippocampus, as galanin (0.35-3 nmol) locally applied had no effect. The results provide in vivo evidence that galanin stimulates the N-methyl-D-aspartate receptor/nitric oxide synthase/cyclic GMP pathway in the ventral hippocampus, which may be of importance in memory processes.

摘要

我们通过在微透析过程中体内测量细胞外环磷酸鸟苷(cGMP)水平,研究了神经肽甘丙肽是否影响大鼠海马体中的一氧化氮合酶/cGMP途径。甘丙肽(2.5和3.5 nmol;脑室内注射)剂量依赖性地升高了腹侧海马体而非背侧海马体的细胞外环磷酸鸟苷水平。3.5 nmol甘丙肽的作用被局部应用河豚毒素阻断,并被高亲和力甘丙肽拮抗剂M40(甘丙肽-[1-12]-Pro3-[Ala-Leu]2-Ala酰胺)抑制。非竞争性N-甲基-D-天冬氨酸受体拮抗剂马来酸氯胺酮(30 μM注入腹侧海马体或0.2 mg/kg,腹腔注射)和竞争性拮抗剂3-([R]-羧基哌嗪-4-基)-丙基-膦酸(注入50 μM),但不是局部灌注AMPA拮抗剂6-硝基-7-氨磺酰基苯并(f)喹喔啉-2,3-二酮(15 μM)消除了甘丙肽在海马体中引起的cGMP反应。一氧化氮合酶抑制剂L-Arg(NO2)-OMe.HCl和7-硝基吲唑单钠盐局部应用可阻断甘丙肽诱导的海马体细胞外环磷酸鸟苷增加。局部应用1H-(1,2,4)恶二唑并(4,3a)喹喔啉-1-酮(一种可溶性鸟苷酸环化酶的选择性抑制剂)也可阻止这种增加。介导cGMP升高的甘丙肽受体位于海马体之外,因为局部应用甘丙肽(0.35 - 3 nmol)没有效果。这些结果提供了体内证据,表明甘丙肽刺激腹侧海马体中的N-甲基-D-天冬氨酸受体/一氧化氮合酶/cGMP途径,这可能在记忆过程中具有重要意义。

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