Department of Psychiatry, Renmin Hospital of Wuhan University, Wuhan 430060, China.
School of Psychology, Faculty of Science, The University of Sydney, Camperdown, Sydney, New South Wales, Australia.
Brain Res Bull. 2024 Sep;215:111007. doi: 10.1016/j.brainresbull.2024.111007. Epub 2024 Jun 8.
Schizophrenia (SCZ) is a severe mental disorder, but its pathogenesis is still unknown, and its clinical treatment effect is very limited. Transient receptor potential vanilloid 1 (TRPV1) channel and the Endocannabinoid System (ECS)have been confirmed to be involved in the pathogenesis of SCZ, although their actions have not been fully clarified yet. The objective is to examine TRPV1 and ECS expression in the blood of schizophrenia patients and investigate their correlation with disease severity.
This is a cross-sectional investigation. Peripheral blood samples were gathered from normal controls (NC, n=37), as well as individuals with schizophrenia, including first episode (n=30) and recurrent (n=30) cases. We employed western blot and ELISA techniques to quantify TRPV1, cannabinoid receptors 1(CB1), anandamide (AEA), and 2-arachidonoylglycerol (2-AG), and assess the severity of the patient's symptoms by means of the PANSS scale.
Compared to NC, TRPV1 levels showed a noticeable decrease in both first episode schizophrenia (f-SCZ group) and recurrent schizophrenia (r-SCZ group) subjects. Additionally, CB1 levels appeared increased in f-SCZ group. Furthermore, 2-AG levels were found to be elevated in both f-SCZ group and r-SCZ group compared to NC, whereas AEA levels were decreased in f-SCZ group but increased in r-SCZ group. Moreover, among schizophrenia patients, TRPV1 demonstrated a negative correlation with negative symptoms. Within r-SCZ subjects, CB1 displayed a negative correlation with relapse number, while 2-AG showed a correlation in the opposite direction.
This study provides initial clinical evidence of changed TRPV1 expression in schizophrenia, potentially linked to negative symptoms. These results suggest a possible dysfunction of TRPV1 and the endocannabinoid system (ECS), which might offer new avenues for medical interventions.
精神分裂症(SCZ)是一种严重的精神障碍,但其发病机制尚不清楚,临床治疗效果非常有限。瞬时受体电位香草素 1(TRPV1)通道和内源性大麻素系统(ECS)已被证实与 SCZ 的发病机制有关,尽管其作用尚未完全阐明。目的是检查精神分裂症患者血液中的 TRPV1 和 ECS 表达,并研究它们与疾病严重程度的相关性。
这是一项横断面研究。采集了正常对照组(NC,n=37)和精神分裂症患者的外周血样本,包括首发(n=30)和复发(n=30)患者。我们采用 Western blot 和 ELISA 技术来定量 TRPV1、大麻素受体 1(CB1)、花生四烯酸乙醇胺(AEA)和 2-花生四烯酸甘油(2-AG),并通过 PANSS 量表评估患者症状的严重程度。
与 NC 相比,首发精神分裂症(f-SCZ 组)和复发精神分裂症(r-SCZ 组)患者的 TRPV1 水平明显降低。此外,f-SCZ 组的 CB1 水平升高。此外,与 NC 相比,f-SCZ 组和 r-SCZ 组的 2-AG 水平升高,而 f-SCZ 组的 AEA 水平降低,r-SCZ 组的 AEA 水平升高。此外,在精神分裂症患者中,TRPV1 与阴性症状呈负相关。在 r-SCZ 患者中,CB1 与复发次数呈负相关,而 2-AG 呈正相关。
本研究提供了 TRPV1 在精神分裂症中表达改变的初步临床证据,可能与阴性症状有关。这些结果表明 TRPV1 和内源性大麻素系统(ECS)可能存在功能障碍,为医学干预提供了新的途径。