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腺苷能药物Ro 5-4864和卡马西平对小鼠缺氧应激诱导的神经毒性的保护作用。

The protective effect of adenosinergic agents, Ro 5-4864 and carbamazepine against hypoxic stress-induced neurotoxicity in mice.

作者信息

Thorat S N, Kulkarni S K

机构信息

Department of Pharmaceutical Sciences, Panjab University, Chandigarh, India.

出版信息

Methods Find Exp Clin Pharmacol. 1990 Jan-Feb;12(1):17-22.

PMID:2314149
Abstract

Mice subjected to hypoxic stress resulted in increased respiratory rate, tremor and convulsions followed by death. The latencies for convulsion and death following hypoxic stress were 33.29 +/- 1.20 and 34.36 +/- 1.16 min, respectively. In the present study effects of adenosinergic agents Ro 5-4864, a "peripheral-type" benzodiazepine receptor agonist, and carbamazepine were studied on hypoxic stress-induced neurotoxicity. Adenosinergic agents such as adenosine, 2-chloroadenosine, N6-cyclohexyladenosine and dipyridamole increased the latencies for convulsions and death due to hypoxia. Theophylline (50 mg/kg i.p.), an adenosine receptor antagonist, reversed this protective effect of adenosinergic agents. Pretreatment with Ro 5-4864 (10, 20 mg/kg i.p.) also offered theophylline (50 mg/kg, i.p.)-sensitive protection against hypoxic stress. Similarly, carbamazepine treatment (10-30 mg/kg, i.p.) significantly prolonged the latencies for convulsion and death following hypoxic stress. Prior treatment with theophylline (50 mg/kg, i.p.) reversed this protective effect of carbamazepine, indicating the possible involvement of adenosinergic mechanism in the observed protective effect of carbamazepine. These results indicate that the adenosinergic mechanism may be responsible for the observed neuroprotective effect of these agents against hypoxia.

摘要

遭受低氧应激的小鼠会出现呼吸频率增加、震颤和惊厥,随后死亡。低氧应激后惊厥和死亡的潜伏期分别为33.29±1.20分钟和34.36±1.16分钟。在本研究中,研究了腺苷能药物Ro 5-4864(一种“外周型”苯二氮䓬受体激动剂)和卡马西平对低氧应激诱导的神经毒性的影响。腺苷、2-氯腺苷、N6-环己基腺苷和双嘧达莫等腺苷能药物增加了低氧引起的惊厥和死亡潜伏期。腺苷受体拮抗剂茶碱(50mg/kg腹腔注射)可逆转腺苷能药物的这种保护作用。Ro 5-4864(10、20mg/kg腹腔注射)预处理也提供了对低氧应激的茶碱(50mg/kg,腹腔注射)敏感的保护作用。同样,卡马西平治疗(10-30mg/kg,腹腔注射)显著延长了低氧应激后惊厥和死亡的潜伏期。茶碱(50mg/kg,腹腔注射)预处理可逆转卡马西平的这种保护作用,表明腺苷能机制可能参与了卡马西平观察到的保护作用。这些结果表明,腺苷能机制可能是这些药物对低氧具有神经保护作用的原因。

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