Xu Hang, Zhang Xiang Yang, Wang Wei Wen, Wang Jiesi
CAS Key Laboratory of Mental Health, Institute of Psychology, Chinese Academy of Sciences, Beijing, China.
Front Pharmacol. 2021 Apr 19;12:633112. doi: 10.3389/fphar.2021.633112. eCollection 2021.
Hydroxychloroquine (HCQ), which has been proposed as a therapeutic or prophylactic drug for COVID-19, has been administered to thousands of individuals with varying efficacy; however, our understanding of its adverse effects is insufficient. It was reported that HCQ induced psychiatric symptoms in a few patients with autoimmune diseases, but it is still uncertain whether HCQ poses a risk to mental health. Therefore, in this study, we treated healthy mice with two different doses of HCQ that are comparable to clinically administered doses for 7 days. Psychiatric-like behaviors and the expression of related molecules in the brain were evaluated at two time points, i.e., 24 h and 10 days after drug administration. We found that HCQ increased anxiety behavior at both 24 h and 10 days. Furthermore, HCQ decreased the mRNA expression of interleukin-1beta, corticotropin-releasing hormone (Crh), a serotonin transporter (Slc6a4), and a microglia maker (Aif1) in the hippocampus and decreased the mRNA expression of brain-derived neurotrophic factor (Bdnf) in both the hippocampus and amygdala. Lots of these behavioral and molecular changes were sustained beyond 10 days after drug administration, and some of them were dose-dependent. Although this animal study does not prove that HCQ has a similar effect in humans, it indicates that HCQ poses a significant risk to mental health and suggests that further clinical investigation is essential. According to our data, we recommend that HCQ be carefully used as a prophylactic drug in people who are susceptible to mental disorders.
羟氯喹啉(HCQ)已被提议作为治疗或预防新冠肺炎的药物,数千人使用过该药,疗效各异;然而,我们对其不良反应的了解并不充分。据报道,HCQ在少数自身免疫性疾病患者中诱发了精神症状,但HCQ是否对心理健康构成风险仍不确定。因此,在本研究中,我们用两种与临床给药剂量相当的不同剂量的HCQ对健康小鼠进行了7天的治疗。在给药后24小时和10天这两个时间点评估了类似精神疾病的行为以及大脑中相关分子的表达。我们发现,HCQ在24小时和10天时均增加了焦虑行为。此外,HCQ降低了海马体中白细胞介素-1β、促肾上腺皮质激素释放激素(Crh)、血清素转运体(Slc6a4)和小胶质细胞标志物(Aif1)的mRNA表达,并降低了海马体和杏仁核中脑源性神经营养因子(Bdnf)的mRNA表达。许多这些行为和分子变化在给药后10天以上仍持续存在,其中一些变化呈剂量依赖性。虽然这项动物研究并未证明HCQ在人类中有类似作用,但它表明HCQ对心理健康构成重大风险,并建议进行进一步的临床研究至关重要。根据我们的数据,我们建议在易患精神障碍的人群中谨慎使用HCQ作为预防药物。