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The effects of nicotine on locomotor activity in non-tolerant and tolerant rats.

机译:尼古丁对非耐受性和耐受性大鼠运动能力的影响。

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摘要

1--Rats were tested for locomotor activity in photocell cages, for 80 min starting immediately after subcutaneous injection of (-)-nicotine bitartrate or 0.9% w/v NaCl solution (saline). In non-tolerant subjects, nicotine (0.1 to 0.4 mg/kg base) depressed activity and induced ataxia in the first 20 min, but increased activity later in the session; these actions were dose-dependent. 2--Tolerance was studied by comparing rats given nicotine (0.4 mg/kg s.c.) every day with control rats given saline instead. Each week, every subject was tested once with nicotine (0.4 mg/kg) and once with saline. With daily or even weekly injections of nicotine, the initial depressant action of the drug was replaced by a dose-dependent stimulant action which occurred throughout the session. In these tolerant animals, little ataxia was seen except when a larger dose of 0.8 mg/kg was given. Tolerance to the depressant action of nicotine persisted for at least 3 weeks. 3--In non-tolerant subjects, mecamylamine (0.5, 1.0 mg/kg s.c.) prevented the initial depressant action of nicotine (0.4 mg/kg). In tolerant rats, the locomotor stimulant action of nicotine (0.4 mg/kg) was prevented by mecamylamine (0.1, 0.32, 1.0 mg/kg s.c.) in a dose-related way; the quaternary ganglion blocker, hexamethonium (0.2, 1.0, 5.0 mg/kg s.c.) had little or no such effect. Neither mecamylamine nor hexamethonium altered activity when given alone. 4--It is suggested that a few treatments with nicotine can unmask a stimulant action of the drug, probably of central origin, which possibly reflects a stimulation of nicotine receptors.
机译:1 ---在皮下注射(-)-烟碱酒石酸氢盐或0.9%w / v NaCl溶液(盐水)后立即开始80分钟,测试大鼠在光电池笼中的运动能力。在非耐受性受试者中,尼古丁(0.1至0.4 mg / kg碱)在开始的20分钟内抑制了活动并诱发了共济失调,但在训练的后期增加了活动。这些动作是剂量依赖性的。通过将每天服用尼古丁(0.4 mg / kg s.c.)的大鼠与服用盐水的对照大鼠进行比较,研究了2耐受性。每周,每位受试者接受烟碱(0.4 mg / kg)测试一次,并接受生理盐水测试一次。通过每天甚至每周一次的尼古丁注射,该药物的最初抑制作用被整个疗程中发生的剂量依赖性刺激作用所代替。在这些耐受的动物中,除了给予0.8 mg / kg的较大剂量外,几乎看不到共济失调。耐尼古丁的抑制作用持续至少3周。 3--在非耐受性受试者中,美卡明胺(0.5,1.0 mg / kg s.c.)阻止了尼古丁的初始镇静作用(0.4 mg / kg)。在耐受性大鼠中,美卡明胺(0.1、0.32、1.0 mg / kg s.c.)以剂量相关的方式阻止了尼古丁(0.4 mg / kg)的运动刺激作用;季神经节阻滞剂六甲铵(0.2、1.0、5.0 mg / kg s.c.)几乎没有这种作用。单独服用美加明胺和六甲铵都不会改变活性。 4--建议使用尼古丁的一些治疗方法可以揭示该药物的刺激作用,可能是中枢起源的,这可能反映了尼古丁受体的刺激。

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