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Effects of Xingnaojing Injection on Adenosinergic Transmission and Orexin Signaling in Lateral Hypothalamus of Ethanol-Induced Coma Rats

Acute alcohol exposure induces unconscious condition such as coma whose main physical manifestation is the loss of righting reflex (LORR). Xingnaojing Injection (XNJI), which came from Chinese classic formula An Gong Niu Huang Pill, is widely used for consciousness disorders in China, such as coma....

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Autores principales: Chen, Xiao-Tong, Wang, Xiao-Ge, Xie, Li-Yuan, Huang, Jia-Wen, Zhao, Wei, Wang, Qi, Yao, Li-Mei, Li, Wei-Rong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6620848/
https://www.ncbi.nlm.nih.gov/pubmed/31346513
http://dx.doi.org/10.1155/2019/2389485
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author Chen, Xiao-Tong
Wang, Xiao-Ge
Xie, Li-Yuan
Huang, Jia-Wen
Zhao, Wei
Wang, Qi
Yao, Li-Mei
Li, Wei-Rong
author_facet Chen, Xiao-Tong
Wang, Xiao-Ge
Xie, Li-Yuan
Huang, Jia-Wen
Zhao, Wei
Wang, Qi
Yao, Li-Mei
Li, Wei-Rong
author_sort Chen, Xiao-Tong
collection PubMed
description Acute alcohol exposure induces unconscious condition such as coma whose main physical manifestation is the loss of righting reflex (LORR). Xingnaojing Injection (XNJI), which came from Chinese classic formula An Gong Niu Huang Pill, is widely used for consciousness disorders in China, such as coma. Although XNJI efficiently shortened the duration of LORR induced by acute ethanol, it remains unknown how XNJI acts on ethanol-induced coma (EIC). We performed experiments to examine the effects of XNJI on orexin and adenosine (AD) signaling in the lateral hypothalamic area (LHA) in EIC rats. Results showed that XNJI reduced the duration of LORR, which implied that XNJI promotes recovery form coma. Microdialysis data indicated that acute ethanol significantly increased AD release in the LHA but had no effect on orexin A levels. The qPCR results displayed a significant reduction in the Orexin-1 receptors (OX(1)R) expression with a concomitant increase in the A(1) receptor (A(1)R) and equilibrative nucleoside transporter type 1 (ENT1) expression in EIC rats. In contrast, XNJI reduced the extracellular AD levels but orexin A levels remained unaffected. XNJI also counteracted the downregulation of the OX(1)R expression and upregulation of A(1)R and ENT1 expression caused by EIC. As for ADK expression, XNJI but not ethanol, displayed an upregulation in the LHA in EIC rats. Based on these results, we suggest that XNJI promotes arousal by inhibiting adenosine neurotransmission via reducing AD level and the expression of A(1)R and ENT1.
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spelling pubmed-66208482019-07-25 Effects of Xingnaojing Injection on Adenosinergic Transmission and Orexin Signaling in Lateral Hypothalamus of Ethanol-Induced Coma Rats Chen, Xiao-Tong Wang, Xiao-Ge Xie, Li-Yuan Huang, Jia-Wen Zhao, Wei Wang, Qi Yao, Li-Mei Li, Wei-Rong Biomed Res Int Research Article Acute alcohol exposure induces unconscious condition such as coma whose main physical manifestation is the loss of righting reflex (LORR). Xingnaojing Injection (XNJI), which came from Chinese classic formula An Gong Niu Huang Pill, is widely used for consciousness disorders in China, such as coma. Although XNJI efficiently shortened the duration of LORR induced by acute ethanol, it remains unknown how XNJI acts on ethanol-induced coma (EIC). We performed experiments to examine the effects of XNJI on orexin and adenosine (AD) signaling in the lateral hypothalamic area (LHA) in EIC rats. Results showed that XNJI reduced the duration of LORR, which implied that XNJI promotes recovery form coma. Microdialysis data indicated that acute ethanol significantly increased AD release in the LHA but had no effect on orexin A levels. The qPCR results displayed a significant reduction in the Orexin-1 receptors (OX(1)R) expression with a concomitant increase in the A(1) receptor (A(1)R) and equilibrative nucleoside transporter type 1 (ENT1) expression in EIC rats. In contrast, XNJI reduced the extracellular AD levels but orexin A levels remained unaffected. XNJI also counteracted the downregulation of the OX(1)R expression and upregulation of A(1)R and ENT1 expression caused by EIC. As for ADK expression, XNJI but not ethanol, displayed an upregulation in the LHA in EIC rats. Based on these results, we suggest that XNJI promotes arousal by inhibiting adenosine neurotransmission via reducing AD level and the expression of A(1)R and ENT1. Hindawi 2019-06-27 /pmc/articles/PMC6620848/ /pubmed/31346513 http://dx.doi.org/10.1155/2019/2389485 Text en Copyright © 2019 Xiao-Tong Chen et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Chen, Xiao-Tong
Wang, Xiao-Ge
Xie, Li-Yuan
Huang, Jia-Wen
Zhao, Wei
Wang, Qi
Yao, Li-Mei
Li, Wei-Rong
Effects of Xingnaojing Injection on Adenosinergic Transmission and Orexin Signaling in Lateral Hypothalamus of Ethanol-Induced Coma Rats
title Effects of Xingnaojing Injection on Adenosinergic Transmission and Orexin Signaling in Lateral Hypothalamus of Ethanol-Induced Coma Rats
title_full Effects of Xingnaojing Injection on Adenosinergic Transmission and Orexin Signaling in Lateral Hypothalamus of Ethanol-Induced Coma Rats
title_fullStr Effects of Xingnaojing Injection on Adenosinergic Transmission and Orexin Signaling in Lateral Hypothalamus of Ethanol-Induced Coma Rats
title_full_unstemmed Effects of Xingnaojing Injection on Adenosinergic Transmission and Orexin Signaling in Lateral Hypothalamus of Ethanol-Induced Coma Rats
title_short Effects of Xingnaojing Injection on Adenosinergic Transmission and Orexin Signaling in Lateral Hypothalamus of Ethanol-Induced Coma Rats
title_sort effects of xingnaojing injection on adenosinergic transmission and orexin signaling in lateral hypothalamus of ethanol-induced coma rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6620848/
https://www.ncbi.nlm.nih.gov/pubmed/31346513
http://dx.doi.org/10.1155/2019/2389485
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