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γ-氨基丁酸、L-谷氨酸和尼古丁对大鼠黑质切片中钾离子诱发的P物质释放的抑制作用。

Inhibitory effects of GABA, L-glutamic acid and nicotine on the potassium-evoked release of substance P in substantia nigra slices of the rat.

作者信息

Torrens Y, Beaujouan J C, Besson M J, Michelot R, Glowinski J

出版信息

Eur J Pharmacol. 1981 May 22;71(4):383-92. doi: 10.1016/0014-2999(81)90182-5.

Abstract

Rat substantia nigra slices were superfused with a physiological medium containing a diluted substance P (SP) antiserum, bacitracin and serum albumin to measure SP released in superfusates. As shown by measuring the degradation of a SP-labelled derivative incubated with cerebellar slices, this medium prevented the enzymatic inactivation of SP. Potassium (K+, 50 mM) and veratridine (5 X 10(-5) M) stimulated SP release and these effects were respectively prevented in absence of calcium and in presence of tetrodotoxin (5 X 10(-7) M). GABA (5 X 10(-5) M), nicotine (10(-6) M) and L-glutamic acid (5 X 10(-5) M) reduced the K+ (50 mM)-evoked release of SP. In contrast, glycine (5 X 10(-5) M), oxotremorine (5 X 10(-5) M), D-glutamic acid (5 X 10(-5) M) and serotonin (5 X 10(-5) M) were without effect. Pempidine (10(-5) M) prevented the inhibitory effect of nicotine (10(-6) M) on the K+-evoked release of SP. Glutamic acid diethyl ester (10(-4) M) completely abolished the L-glutamic acid-induced inhibition of the K+-evoked release of SP. Picrotoxin (5 X 10(-5) M) did not influence the L-glutamic acid inhibitory effect excluding the intervention of GABAergic mechanisms.

摘要

用含有稀释的P物质(SP)抗血清、杆菌肽和血清白蛋白的生理介质对大鼠黑质切片进行灌流,以测量灌流液中释放的SP。通过测量与小脑切片一起孵育的SP标记衍生物的降解情况表明,这种介质可防止SP的酶促失活。钾离子(K +,50 mM)和藜芦定(5×10(-5)M)刺激SP释放,在无钙和存在河豚毒素(5×10(-7)M)的情况下,这些作用分别受到抑制。γ-氨基丁酸(GABA,5×10(-5)M)、尼古丁(10(-6)M)和L-谷氨酸(5×10(-5)M)可减少K +(50 mM)诱发的SP释放。相反,甘氨酸(5×10(-5)M)、氧化震颤素(5×10(-5)M)、D-谷氨酸(5×10(-5)M)和5-羟色胺(5×10(-5)M)则无作用。潘必啶(10(-5)M)可防止尼古丁(10(-6)M)对K +诱发的SP释放的抑制作用。谷氨酸二乙酯(10(-4)M)完全消除了L-谷氨酸对K +诱发的SP释放的抑制作用。印防己毒素(5×10(-5)M)不影响L-谷氨酸的抑制作用,排除了GABA能机制的干预。

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