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可卡因经口给药与皮下给药对雌性大鼠行为、血浆药物浓度及毒性的比较。

Comparison of oral and subcutaneous routes of cocaine administration on behavior, plasma drug concentration and toxicity in female rats.

作者信息

Dow-Edwards D, Fico T A, Osman M, Gamagaris Z, Hutchings D E

机构信息

State University of New York, Health Science Center, Brooklyn 11203.

出版信息

Pharmacol Biochem Behav. 1989 May;33(1):167-73. doi: 10.1016/0091-3057(89)90446-2.

Abstract

Oral and subcutaneous routes of administration of cocaine HCl were investigated in female Wistar rats for food and water consumption, locomotor activity, stereotypic behaviors, plasma drug concentrations and injection site pathology. Animals received either 40 or 80 mg/kg/day by gastric intubation (PO-40 and PO-80 respectively) or 20 or 40 mg/kg/day subcutaneously (SC-20 and SC-40). All groups received the drug or the vehicle for 16 consecutive days. Locomotor activity and stereotypy were evaluated on Days 1, 5, 10, and 15. Plasma drug concentrations and injection site pathology were determined on Day 16. Subcutaneous administration was associated with a sensitization to the effects of cocaine on locomotion and stereotypy, higher blood levels than oral administration at the same dose, and severe dermal lesions. However, there were no differences in any measure between the SC-20 and SC-40 groups. Oral cocaine was also associated with behavioral sensitization. However, unlike the SC route, oral cocaine was characterized by dose-related increases in locomotion and stereotypy in the absence of gastrointestinal pathology. Inasmuch as oral administration resulted in dose-response relationships and low toxicity while subcutaneous administration did not, these factors should be considered in future studies utilizing chronic cocaine administration.

摘要

在雌性Wistar大鼠中研究了盐酸可卡因的口服和皮下给药途径对食物和水消耗、运动活动、刻板行为、血浆药物浓度及注射部位病理学的影响。动物通过胃插管分别接受40或80mg/kg/天(分别为PO - 40和PO - 80)或皮下接受20或40mg/kg/天(SC - 20和SC - 40)。所有组连续16天接受药物或赋形剂。在第1、5、10和15天评估运动活动和刻板行为。在第16天测定血浆药物浓度和注射部位病理学。皮下给药与对可卡因运动和刻板行为作用的敏化、相同剂量下比口服给药更高的血药水平以及严重的皮肤损伤有关。然而,SC - 20和SC - 40组之间在任何测量指标上均无差异。口服可卡因也与行为敏化有关。然而,与皮下给药途径不同,口服可卡因的特点是在无胃肠道病理学情况下运动和刻板行为呈剂量相关增加。由于口服给药产生了剂量反应关系且毒性低,而皮下给药则不然,在未来利用慢性可卡因给药的研究中应考虑这些因素。

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