首页> 外文期刊>Progress in Neuro-Psychopharmacology & Biological Psychiatry: An International Research, Review and News Journal >Effects of NG-nitro-L-arginine methyl ester, 7-nitro indazole, and agmatine on pentylenetetrazol-induced discriminative stimulus in Long-Evans rats.
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Effects of NG-nitro-L-arginine methyl ester, 7-nitro indazole, and agmatine on pentylenetetrazol-induced discriminative stimulus in Long-Evans rats.

机译:NG-硝基-L-精氨酸甲酯,7-硝基吲唑和胍丁胺对戊四氮诱导的Long-Evans大鼠歧视性刺激的影响。

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摘要

This study was undertaken to determine any role that nitric oxide (NO) may play in the discriminative stimuli produced by pentylenetetrazol (PTZ). The PTZ-induced discriminative stimulus is pharmacologically similar to anxiety in humans and is used in a behavioral assay of anxiety (the PTZ model of anxiety). In the present study, effects of L-N(G)-nitro arginine methyl ester (L-NAME), 7-nitroindazole (7-NI) and agmatine, NO synthase (NOS) inhibitors, on PTZ-induced discriminative stimulus were investigated in male Long-Evans rats (330-350 g). Rats were trained to discriminate PTZ (16 mg/kg) from saline using a two-lever, food-reinforced choice procedure (FR 10). The rats that met the training criteria were injected with L-NAME (15, 30, and 60 mg/kg), 7-NI (15 and 30 mg/kg), agmatine (20, 40, and 60 mg/kg), and saline or vehicle intraperitoneally before each test. They were tested for the PTZ-discrimination to determine if the NOS inhibitors produce discriminative stimulus similar to PTZ or if they block PTZ-induced discrimination. Treatment with the NOS inhibitory drugs neither substituted for PTZ nor altered the PTZ lever selection in any other way. These findings suggest that PTZ-induced discriminative stimulus may not be related to NO-mediated central mechanisms.
机译:进行这项研究是为了确定一氧化氮(NO)在戊四氮(PTZ)产生的歧视性刺激中可能发挥的作用。 PTZ诱导的歧视性刺激在药理学上类似于人类的焦虑,并用于焦虑的行为分析(PTZ焦虑模型)。在本研究中,研究了LN(G)-硝基精氨酸甲酯(L-NAME),7-硝基吲唑(7-NI)和胍丁胺,NO合酶(NOS)抑制剂对男性PTZ诱导的歧视性刺激的影响。长埃文斯大鼠(330-350克)。使用两杆食物强化选择程序(FR 10)对大鼠进行训练,使其可从盐水中区分PTZ(16 mg / kg)。符合训练标准的大鼠分别注射L-NAME(15、30和60 mg / kg),7-NI(15和30 mg / kg),胍丁胺(20、40和60 mg / kg),每次测试前腹膜内注射生理盐水或媒介。对他们进行了PTZ歧视测试,以确定NOS抑制剂是否产生类似于PTZ的歧视性刺激,或者它们是否阻止PTZ引起的歧视。用NOS抑制药物进行治疗既不能替代PTZ,也不能以任何其他方式改变PTZ杠杆的选择。这些发现表明,PTZ诱导的歧视性刺激可能与NO介导的中枢机制无关。

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