Bhattacharya S K, Mitra S K
Department of Pharmacology, Banaras Hindu University, Varanasi, India.
Indian J Exp Biol. 1992 Jan;30(1):33-7.
Quinine, a cinchona alkaloid, was investigated for putative anxiogenic activity in view of clinical reports suggesting that it induces anxiety and apprehension following its use in malaria. The experimental paradigms chosen to elucidate anxiogenic activity have been shown to stand the tests of reliability and validity. Yohimbine, which has been shown to induce anxiety both in animals and in man, was used for comparison. Quinine was found to elicit a complex behavioural profile of activity ranging from overt central stimulation to marked central depression on dose increment. The doses 10 and 20 mg/kg, ip, of quinine chosen to investigate anxiogenic activity were comparable to those induced by 2.5 and 5 mg/kg ip of yohimbine. Quinine induced a dose-related anxiogenic activity in the open-field and elevated plus-maze tests in mice, and the social interaction and thirst conflict tests in rats, similar to effects induced by yohimbine. In addition, both quinine and yohimbine attenuated the effects of diazepam, an anxiolytic agent, in the open-field and thirst conflict tests. The results indicate that quinine exerts significant anxiogenic effect at a particular dose range.
鉴于有临床报告表明奎宁在用于治疗疟疾后会引发焦虑和忧虑,因此对金鸡纳生物碱奎宁的潜在致焦虑活性进行了研究。为阐明致焦虑活性而选择的实验范式已被证明经得起可靠性和有效性的检验。已证明育亨宾在动物和人类中均会引发焦虑,因此将其用作对照。研究发现,随着剂量增加,奎宁会引发一系列复杂的行为表现,从明显的中枢兴奋到显著的中枢抑制。为研究致焦虑活性而选择的奎宁腹腔注射剂量为10和20毫克/千克,与2.5和5毫克/千克腹腔注射育亨宾所诱导的剂量相当。在小鼠的旷场试验和高架十字迷宫试验以及大鼠的社交互动试验和口渴冲突试验中,奎宁诱导出与剂量相关的致焦虑活性,类似于育亨宾所诱导的效应。此外,在旷场试验和口渴冲突试验中,奎宁和育亨宾均减弱了抗焦虑药地西泮的作用。结果表明,奎宁在特定剂量范围内具有显著的致焦虑作用。