Kajero Jaiyeola Abiola, Seedat Soraya, Ohaeri Jude U, Akindele Abidemi, Aina Oluwagbemiga
Federal Neuropsychiatric Hospital Yaba, 8, Harvey Road Yaba, P.M.B 2008, Lagos, Nigeria.
Department of Psychiatry, Faculty of Medicine and Health Sciences, Stellenbosch University, Francie van Zijl Drive Tygerberg, Cape Town, 7505, South Africa.
Discov Ment Health. 2022 Jul 14;2(1):18. doi: 10.1007/s44192-022-00021-2.
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.
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.
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.
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.
氟哌啶醇的给药持续时间(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持续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)是否对氟哌啶醇引起的体重变化和FBS升高有任何假定的缓解作用。
氟哌啶醇(5毫克/千克/天)通过腹腔注射(IP)途径给药21天(亚慢性给药),或通过肌肉注射(IM)途径每月给药一次(50毫克/千克/月),持续3个月(慢性给药),单独给药或在CBD(5毫克/千克/天)之前给药。单独口服CBD(5毫克/千克/天)和单独蒸馏水给药21天。在给予药理剂(对照组为蒸馏水)之前和给药后测量体重和FBS。
不同时间点的平均体重组间差异显著。两两比较显示,单独使用亚慢性(IP)氟哌啶醇组(A组)和CBD给药前慢性(IM)氟哌啶醇组(F组)的平均体重随时间显著增加。给药后,亚慢性(IP)氟哌啶醇组的平均FBS与CBD给药前亚慢性(IP)氟哌啶醇组相比显著增加。仅对照组的平均FBS较基线有显著降低。
我们证明氟哌啶醇的给药持续时间会影响大鼠的体重和FBS,表明代谢副作用可能受给药持续时间的影响。CBD改善了亚慢性(IP)氟哌啶醇组中观察到的体重和FBS增加。