大麻二酚对慢性和亚慢性氟哌啶醇给药时体重和空腹血糖的影响

Jaiyeola Abiola Kajero, Soraya Seedat, Jude U Ohaeri, Abidemi Akindele, Oluwagbemiga Aina
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引用次数: 0

摘要

目的:氟哌啶醇的给药时间(如亚慢性或慢性)可能会影响其不良反应。我们研究了氟哌啶醇给药时间对体重和空腹血糖(FBS)的影响。此外,我们还研究了口服大麻二酚(CBD)是否对氟哌啶醇诱导的体重变化和FBS升高有任何公认的缓解作用。方法:氟哌啶醇(5 mg/kg/天)通过腹膜内(IP)途径给药21天(亚慢性给药),或通过肌内(IM)途径每月(50 mg/kg每月)给药3个月(慢性给药,单独给药或在CBD(5 mg/kg/天)之前给药。单独口服CBD(5mg/kg/天)和单独蒸馏水给药21天。在给药前(对照组为蒸馏水)和给药后测量体重和FBS。结果:不同时间组的平均体重差异显著。成对比较显示,单独亚慢性(IP)氟哌啶醇组(A组)和CBD前慢性(IM)氟哌啶酮组(F组)的平均重量随时间显著增加。用药后,亚慢性(IP)氟哌啶醇组的平均FBS与CBD前的亚慢性(IP)氟哌啶醇组相比显著增加。仅对照组的平均FBS也比基线显著降低。结论:我们证明氟哌啶醇的给药时间会影响大鼠的体重和FBS,这表明代谢副作用可能受到给药时间的影响。CBD改善了亚慢性(IP)氟哌啶醇组中观察到的体重和FBS的增加。
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Effects of cannabidiol on weight and fasting blood sugar with chronic and subchronic haloperidol administration.

Objectives: The duration of administration (e.g., subchronic or chronic) of haloperidol may influence its adverse effects. We studied the effects of duration of administration of haloperidol on body weight and fasting blood sugar (FBS). In addition, we examined whether orally administered cannabidiol (CBD) had any putative mitigating influence on haloperidol-induced body weight changes and FBS elevation.

Methods: Haloperidol (5 mg/kg/day) was administered for 21 days (subchronic administration), via the intraperitoneal (IP) route, or monthly (50 mg/kg monthly) for 3 months (chronic administration), via the intramuscular (IM) route, either alone or before CBD (5 mg/kg/day). Oral CBD (5 mg/kg/day) alone and distilled water alone were administered for 21 days. Weight and FBS were measured before administration of pharmacological agents (distilled water in the control group) and post-administration.

Results: Group differences in average weight across time were significant. Pairwise comparisons showed that mean weight of the subchronic (IP) haloperidol alone group (Group A) and the chronic (IM) haloperidol before CBD group (Group F) increased significantly over time. Post medications, there was a significant increase in mean FBS in the subchronic (IP) haloperidol group compared to the subchronic (IP) haloperidol before CBD group. There was also a significant reduction in mean FBS from the baseline for the control group only.

Conclusion: We demonstrated that the duration of administration of haloperidol influenced weight and FBS in rats, suggesting that metabolic side effects, may be influenced by duration of administration. CBD ameliorated the increase in weight and FBS observed in the subchronic (IP) haloperidol groups.

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