Cargando…
Naringin Relieves Diabetic Cardiac Autonomic Neuropathy Mediated by P2Y(14) Receptor in Superior Cervical Ganglion
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 cervic...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9068893/ https://www.ncbi.nlm.nih.gov/pubmed/35529431 http://dx.doi.org/10.3389/fphar.2022.873090 |
_version_ | 1784700315514175488 |
---|---|
author | 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 |
author_facet | 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 |
author_sort | Tang, Gan |
collection | PubMed |
description | 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(14) and IL-1β in diabetic rats, both of which were remarkably diminished by treatment with either P2Y(14) 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(14) 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(14)-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. |
format | Online Article Text |
id | pubmed-9068893 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90688932022-05-05 Naringin Relieves Diabetic Cardiac Autonomic Neuropathy Mediated by P2Y(14) Receptor in Superior Cervical Ganglion 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 Front Pharmacol Pharmacology 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(14) and IL-1β in diabetic rats, both of which were remarkably diminished by treatment with either P2Y(14) 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(14) 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(14)-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. Frontiers Media S.A. 2022-04-21 /pmc/articles/PMC9068893/ /pubmed/35529431 http://dx.doi.org/10.3389/fphar.2022.873090 Text en Copyright © 2022 Tang, Pi, Guo, Hu, Zhou, Hu, Peng, Xiao, Zhang, Wang, Peng, Huang, Liang and Li. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology 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 Naringin Relieves Diabetic Cardiac Autonomic Neuropathy Mediated by P2Y(14) Receptor in Superior Cervical Ganglion |
title | Naringin Relieves Diabetic Cardiac Autonomic Neuropathy Mediated by P2Y(14) Receptor in Superior Cervical Ganglion |
title_full | Naringin Relieves Diabetic Cardiac Autonomic Neuropathy Mediated by P2Y(14) Receptor in Superior Cervical Ganglion |
title_fullStr | Naringin Relieves Diabetic Cardiac Autonomic Neuropathy Mediated by P2Y(14) Receptor in Superior Cervical Ganglion |
title_full_unstemmed | Naringin Relieves Diabetic Cardiac Autonomic Neuropathy Mediated by P2Y(14) Receptor in Superior Cervical Ganglion |
title_short | Naringin Relieves Diabetic Cardiac Autonomic Neuropathy Mediated by P2Y(14) Receptor in Superior Cervical Ganglion |
title_sort | naringin relieves diabetic cardiac autonomic neuropathy mediated by p2y(14) receptor in superior cervical ganglion |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9068893/ https://www.ncbi.nlm.nih.gov/pubmed/35529431 http://dx.doi.org/10.3389/fphar.2022.873090 |
work_keys_str_mv | AT tanggan naringinrelievesdiabeticcardiacautonomicneuropathymediatedbyp2y14receptorinsuperiorcervicalganglion AT pilingzhi naringinrelievesdiabeticcardiacautonomicneuropathymediatedbyp2y14receptorinsuperiorcervicalganglion AT guohongmin naringinrelievesdiabeticcardiacautonomicneuropathymediatedbyp2y14receptorinsuperiorcervicalganglion AT huzihui naringinrelievesdiabeticcardiacautonomicneuropathymediatedbyp2y14receptorinsuperiorcervicalganglion AT zhoucongfa naringinrelievesdiabeticcardiacautonomicneuropathymediatedbyp2y14receptorinsuperiorcervicalganglion AT huqixing naringinrelievesdiabeticcardiacautonomicneuropathymediatedbyp2y14receptorinsuperiorcervicalganglion AT penghao naringinrelievesdiabeticcardiacautonomicneuropathymediatedbyp2y14receptorinsuperiorcervicalganglion AT xiaozehao naringinrelievesdiabeticcardiacautonomicneuropathymediatedbyp2y14receptorinsuperiorcervicalganglion AT zhangzhihua naringinrelievesdiabeticcardiacautonomicneuropathymediatedbyp2y14receptorinsuperiorcervicalganglion AT wangmiaomiao naringinrelievesdiabeticcardiacautonomicneuropathymediatedbyp2y14receptorinsuperiorcervicalganglion AT pengtaotao naringinrelievesdiabeticcardiacautonomicneuropathymediatedbyp2y14receptorinsuperiorcervicalganglion AT huangjiaqi naringinrelievesdiabeticcardiacautonomicneuropathymediatedbyp2y14receptorinsuperiorcervicalganglion AT liangshangdong naringinrelievesdiabeticcardiacautonomicneuropathymediatedbyp2y14receptorinsuperiorcervicalganglion AT liguilin naringinrelievesdiabeticcardiacautonomicneuropathymediatedbyp2y14receptorinsuperiorcervicalganglion |