Nax-positive glial cells in the organum vasculosum laminae terminalis produce epoxyeicosatrienoic acids to induce water intake in response to increases in [Na+] in body fluids

被引:9
作者
Sakuta, Hiraki [1 ,2 ]
Lin, Chia-Hao [1 ]
Yamada, Masaki [3 ,4 ]
Kita, Yoshihiro [3 ]
Tokuoka, Suzumi M. [3 ]
Shimizu, Takao [3 ,5 ]
Noda, Masaharu [1 ,2 ,6 ]
机构
[1] Natl Inst Basic Biol, Div Mol Neurobiol, 5-1 Higashiyama,Myodaiji Cho, Okazaki, Aichi 4448787, Japan
[2] Grad Univ Adv Studies, Sch Life Sci, Okazaki, Aichi 4448787, Japan
[3] Univ Tokyo, Fac Med, Dept Lipid, Tokyo 1130033, Japan
[4] Shimadzu Co Ltd, Kyoto 6048511, Japan
[5] Natl Ctr Global Hlth & Med, Res Inst, Dept Lipid Signaling, Tokyo 1628655, Japan
[6] Tokyo Inst Technol, Inst Innovat Res, Cell Biol Ctr, Yokohama, Kanagawa 2268503, Japan
基金
日本学术振兴会;
关键词
Epoxyeicosatrienoic acids; Naxorganum vasculosum laminae terminalis; Water intake; Cyp2c44; TRPV4; SODIUM-LEVEL SENSOR; SUBFORNICAL ORGAN; ARACHIDONIC-ACID; VASOPRESSIN SECRETION; INDUCED DRINKING; BRAIN; EXPRESSION; LESIONS; THIRST; EPOXYGENASE;
D O I
10.1016/j.neures.2019.05.006
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Nax is a [Na+] sensor expressed in specific glial cells in the sensory circumventricular organs (sCVOs) in the brain. We recently demonstrated that Nax signals are involved in the control of not only salt intake but also water intake behavior. Our pharmacological experiments suggested that Na-x signals led to activation of neurons bearing TRPV4 by using epoxyeicosatrienoic acids (EETs) as gliotransmitters to stimulate water intake. In the present study, we performed selective lesions of individual sCVOs in wild -type (WT) mice and the site-directed rescue of Na, expression in Na-x-gene knockout (Na-x-KO) mice. These experiments revealed that the Nax channel in the organum vasculosum laminae terminalis (OVLT) functions as a [Na+] sensor for the control of water intake behavior. Direct measurements of 5,6-EET and 8,9-EET in the OVLT demonstrated that EET levels were indeed increased two-fold by water deprivation for two days in WT, but not Na-x-KO mice, indicating that EETs were Na-x-dependently produced in the OVLT in response to increases in [Na+] in body fluids. More importantly, intracerebroventricular injection of 5,6-EET at the same level was effective to induce water intake. Double staining revealed that Na-x-positive cells also expressed Cyp2c44, a cytochrome P450 epoxygenase, to generate EETs. Collectively, these results indicate that Na-x-positive glial cells produce EETs to activate TRPV4-positive neurons which may stimulate water intake, in response to increases in [Na+] of body fluids. (C) 2019 Elsevier B.V. and Japan Neuroscience Society. All rights reserved.
引用
收藏
页码:45 / 51
页数:7
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