Role of group II and III mGluRs in carotid body plasticity induced by chronic intermittent hypoxia in rats.
- Author:
Chen-Lu ZHAO
1
;
Chao-Hong LI
1
;
Yu-Zhen LIU
2
Author Information
1. The First Affiliated Hospital of Xinxiang Medical University, Henan Key Laboratory of Neural Repairment, Life Sciences Research Center, Weihui 453100, China.
2. The First Affiliated Hospital of Xinxiang Medical University, Henan Key Laboratory of Neural Repairment, Life Sciences Research Center, Weihui 453100, China. yuzhenliu@xxmu.edu.cn.
- Publication Type:Journal Article
- MeSH:
Rats;
Animals;
Carotid Body/metabolism*;
Rats, Sprague-Dawley;
Hypoxia;
Receptors, Metabotropic Glutamate/metabolism*;
RNA, Messenger/metabolism*
- From:
Acta Physiologica Sinica
2023;75(4):529-536
- CountryChina
- Language:Chinese
-
Abstract:
The aim of the present study was to explore the role of group II and III metabotropic glutamate receptors (mGluRs) in carotid body plasticity induced by chronic intermittent hypoxia (CIH) in rats. Sprague Dawley (SD) rats were treated with CIH in Oxycycler A84 hypoxic chamber for 4 weeks, and the tail artery blood pressure was measured at the end of model preparation. RT-qPCR was performed to examine the mRNA expression levels of mGluR2/3/8 in rat carotid body. Carotid sinus nerve activity was detected by ex vivo carotid sinus nerve discharge recording technique, and acute intermittent hypoxia (AIH) was administered to induce carotid body sensory long-term facilitation (sLTF), in order to observe the role of group II and group III mGluRs in carotid body plasticity induced by CIH. The results showed that: 1) After 4 weeks of CIH exposure, the blood pressure of rats increased significantly; 2) CIH down-regulated the mRNA levels of mGluR2/3, and up-regulated the mRNA level of mGluR8 in the carotid body; 3) AIH induced sLTF in carotid body of CIH group. In the CIH group, activation of group II mGluRs had no effect on sLTF of carotid body, while activation of group III mGluRs completely inhibited sLTF. These results suggest that CIH increases blood pressure in rats, and group III mGluRs play an inhibitory role in CIH-induced carotid body plasticity in rats.
