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硝苯地平单次及长期给药对大鼠痛觉和刻板行为的影响。

Effects of single and long-term administration of nifedipine on nociception and stereotyped behavior of rats.

作者信息

Mattia N F, Maiolini Júnior M, Conceição I M, Chang Y H, Smaili S, Frussa-Filho R

机构信息

Departamento de Farmacologia, Escola Paulista de Medicina, São Paulo, Brasil.

出版信息

Braz J Med Biol Res. 1994 Mar;27(3):719-23.

PMID:8081296
Abstract

In the present investigation, nociception and stereotyped behavior were evaluated in 3-month old male Wistar rats after a single nifedipine dose (2.5 and 5.0 mg/kg, ip, 1 h before testing, 6-7 rats per group for stereotypy studies and 15 animals per group for nociception experiments) or after long-term nifedipine treatment (2.5 mg/kg, ip, twice daily for 30 days, with testing performed 72 or 96 h after the last injection, 7 rats per group for stereotypy studies and 14-16 animals per group for nociception experiments). Stereotypy was induced with 2.5 mg/kg amphetamine, ip, and nociception was measured by the tail-immersion test. Administration of a single nifedipine dose did not modify nociception or amphetamine-induced stereotypy (with a mean +/- SEM tail-withdrawal latency of 4.5 +/- 0.5 s for control, 4.4 +/- 0.3 s for 2.5 mg/kg nifedipine and 4.7 +/- 0.7 s for 5.0 mg/kg nifedipine and with mean +/- SEM sum of stereotypy scores of 32.5 +/- 1.6 for control, 29.1 +/- 1.0 for 2.5 mg/kg nifedipine and 29.1 +/- 1.6 for 5.0 mg/kg nifedipine). Withdrawal from long-term nifedipine treatment did not affect stereotyped behavior (with mean +/- SEM sum of stereotypy scores of 28.7 +/- 1.6 for control and 30.7 +/- 1.3 for nifedipine-treated rats) but significantly increased tail-withdrawal latencies (with a mean +/- SEM tail-withdrawal latency of 4.1 +/- 0.3 s for control and 6.4 +/- 0.6 s for nifedipine-treated rats). Therefore, long-term nifedipine treatment induced plastic modifications in nociception but not in stereotyped behavior.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在本研究中,对3月龄雄性Wistar大鼠在单次给予硝苯地平(剂量为2.5和5.0mg/kg,腹腔注射,测试前1小时给药,每组6 - 7只大鼠用于刻板行为研究,每组15只动物用于伤害感受实验)或长期给予硝苯地平治疗后(2.5mg/kg,腹腔注射,每日两次,共30天,在最后一次注射后72或96小时进行测试,每组7只大鼠用于刻板行为研究,每组14 - 16只动物用于伤害感受实验)的伤害感受和刻板行为进行了评估。用2.5mg/kg苯丙胺腹腔注射诱导刻板行为,通过尾浸试验测量伤害感受。单次给予硝苯地平剂量并未改变伤害感受或苯丙胺诱导的刻板行为(对照组平均±标准误尾缩潜伏期为4.5±0.5秒,2.5mg/kg硝苯地平组为4.4±0.3秒,5.0mg/kg硝苯地平组为4.7±0.7秒;对照组刻板行为评分总和平均±标准误为32.5±1.6,2.5mg/kg硝苯地平组为29.1±1.0,5.0mg/kg硝苯地平组为29.1±1.6)。长期硝苯地平治疗撤药后并未影响刻板行为(对照组刻板行为评分总和平均±标准误为28.7±1.6,硝苯地平治疗组大鼠为30.7±1.3),但显著增加了尾缩潜伏期(对照组平均±标准误尾缩潜伏期为4.1±0.3秒,硝苯地平治疗组大鼠为6.4±0.6秒)。因此,长期硝苯地平治疗在伤害感受方面诱导了可塑性改变,但在刻板行为方面未诱导改变。(摘要截短至250字)

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