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首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Participation of nitric oxide and N-methyl-D-aspartic acid receptors in the pressor response to intrathecal injected noradrenaline at the spinal cord of the rat.
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Participation of nitric oxide and N-methyl-D-aspartic acid receptors in the pressor response to intrathecal injected noradrenaline at the spinal cord of the rat.

机译:一氧化氮和N-甲基-D-天冬氨酸受体参与大鼠脊髓鞘内注射去甲肾上腺素的升压反应。

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摘要

In pentobarbital-anesthetized rats, intrathecal injection of noradrenaline (NA; 6, 18 and 60 nmol) induced a dose-dependent increase in the mean blood pressure. The pressor response to NA (18 nmol) was blocked by pretreatment with the selective antagonist for N-methyl-D-aspartic acid (NMDA) receptors, 2-amino-5-phosphonovaleric acid (30 nmol), but not by pretreatment with the selective antagonist for (+/-)-alpha-amino-3-hydroxy-5-methylisoxazole-4-propionic acid/kainate receptors, 6,7-dinitroquinoxaline-2,3-dione (50 nmol). The pressor effect of NA was reduced after pretreatment with N(G)-nitro-L-arginine methyl ester (L-NAME, 1 micromol). The effect of L-NAME on the pressor response to NA was reverted by the precursor of nitric oxide (NO), L-arginine (5 micromol). The hypertension induced by NA was also reduced by the guanylate cyclase inhibitor methylene blue (0.3 micromol). These results suggest that spinal NMDA receptors and spinal NO are involved in the pressor response to NA.
机译:在戊巴比妥麻醉的大鼠中,鞘内注射去甲肾上腺素(NA; 6、18和60 nmol)引起平均血压的剂量依赖性升高。用N-甲基-D-天冬氨酸(NMDA)受体选择性拮抗剂2-氨基-5-膦酰戊酸(30 nmol)预处理可阻断对NA(18 nmol)的升压反应,但可不使用N-甲基-D-天冬氨酸(30 nmol)预处理。 (+/-)-α-氨基-3-羟基-5-甲基异恶唑-4-丙酸/海藻酸酯受体,6,7-二硝基喹喔啉-2,3-二酮(50 nmol)的选择性拮抗剂。用N(G)-硝基-L-精氨酸甲酯(L-NAME,1微摩尔)预处理后,NA的升压作用降低。一氧化氮(NO)的前体L-精氨酸(5 micromol)还原了L-NAME对NA的升压反应的影响。鸟苷酸环化酶抑制剂亚甲基蓝(0.3微摩尔)也可减轻由NA引起的高血压。这些结果表明,脊髓NMDA受体和脊髓NO参与了对NA的加压反应。

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