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柚皮苷缓解由颈上神经节P2Y受体介导的糖尿病性心脏自主神经病变。

Naringin Relieves Diabetic Cardiac Autonomic Neuropathy Mediated by P2Y Receptor in Superior Cervical Ganglion.

作者信息

Tang Gan, Pi Lingzhi, Guo Hongmin, Hu Zihui, Zhou Congfa, Hu Qixing, Peng Hao, Xiao Zehao, Zhang Zhihua, Wang Miaomiao, Peng Taotao, Huang Jiaqi, Liang Shangdong, Li Guilin

机构信息

Queen Mary School, Medical School of Nanchang University, Nanchang, China.

School of Basic Medicine, Medical School of Nanchang University, Nanchang, China.

出版信息

Front Pharmacol. 2022 Apr 21;13:873090. doi: 10.3389/fphar.2022.873090. eCollection 2022.

Abstract

Diabetes mellitus (DM), an emerging chronic epidemic, contributes to mortality and morbidity around the world. Diabetic cardiac autonomic neuropathy (DCAN) is one of the most common complications associated with DM. Previous studies have shown that satellite glial cells (SGCs) in the superior cervical ganglia (SCG) play an indispensable role in DCAN progression. In addition, it has been shown that purinergic neurotransmitters, as well as metabotropic GPCRs, are involved in the pathophysiological process of DCAN. Furthermore, one traditional Chinese medicine, naringin may potently alleviate the effects of DCAN. Ferroptosis may be involved in DCAN progression. However, the role of naringin in DCAN as well as its detailed mechanism requires further investigation. In this research, we attempted to identify the effect and relevant mechanism of naringin in DCAN mitigation. We observed that compared with those of normal subjects, there were significantly elevated expression levels of P2Y and IL-1β in diabetic rats, both of which were remarkably diminished by treatment with either P2Y shRNA or naringin. In addition, abnormalities in blood pressure (BP), heart rate (HR), heart rate variability (HRV), sympathetic nerve discharge (SND), and cardiac structure in the diabetic model can also be partially returned to normal through the use of those treatments. Furthermore, a reduced expression of NRF2 and GPX4, as well as an elevated level of ROS, were detected in diabetic cases, which can also be improved with those treatments. Our results showed that naringin can effectively relieve DCAN mediated by the P2Y receptor of SGCs in the SCG. Moreover, the NRF2/GPX4 pathway involved in ferroptosis may become one of the principal mechanisms participating in DCAN progression, which can be modulated by P2Y-targeted naringin and thus relieve DCAN. Hopefully, our research can supply one novel therapeutic target and provide a brilliant perspective for the treatment of DCAN.

摘要

糖尿病(DM)作为一种日益普遍的慢性流行病,在全球范围内导致了较高的死亡率和发病率。糖尿病性心脏自主神经病变(DCAN)是与DM相关的最常见并发症之一。先前的研究表明,颈上神经节(SCG)中的卫星神经胶质细胞(SGCs)在DCAN进展中起着不可或缺的作用。此外,已有研究表明,嘌呤能神经递质以及代谢型G蛋白偶联受体(GPCRs)参与了DCAN的病理生理过程。此外,一种传统中药柚皮苷可能有效减轻DCAN的影响。铁死亡可能参与了DCAN的进展。然而,柚皮苷在DCAN中的作用及其详细机制仍需进一步研究。在本研究中,我们试图确定柚皮苷在减轻DCAN方面的作用及相关机制。我们观察到,与正常受试者相比,糖尿病大鼠中P2Y和IL-1β的表达水平显著升高,而用P2Y短发夹RNA(shRNA)或柚皮苷治疗后,这两者均显著降低。此外,通过这些治疗,糖尿病模型中的血压(BP)、心率(HR)、心率变异性(HRV)、交感神经放电(SND)和心脏结构异常也可部分恢复正常。此外,在糖尿病病例中检测到NRF2和GPX4的表达降低以及活性氧(ROS)水平升高,这些也可通过这些治疗得到改善。我们的结果表明,柚皮苷可以有效缓解由SCG中SGCs的P2Y受体介导的DCAN。此外,参与铁死亡的NRF2/GPX4途径可能成为参与DCAN进展的主要机制之一,该途径可被靶向P2Y的柚皮苷调节,从而缓解DCAN。希望我们的研究能够提供一个新的治疗靶点,并为DCAN的治疗提供一个良好的前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dba/9068893/dfa3d9bf0775/fphar-13-873090-g001.jpg

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