The Role of Prostaglandin E2 Synthesized in Rat Lateral Parabrachial Nucleus in LPS-Induced Fever

被引:5
作者
Cheng, Yongjing [1 ]
Xu, Jianhui [1 ]
Zeng, Ruixin [2 ]
Zhao, Xi [3 ]
Gao, Wenmin [1 ]
Quan, Junru [3 ]
Hu, Xiaosong [4 ]
Shen, Ziling [4 ]
Zhang, Jie [1 ]
机构
[1] Chengdu Med Coll, Key Lab Thermoregulat & Inflammat Sichuan Higher, Chengdu, Peoples R China
[2] Zunyi Med Univ, Sch Dent, Zunyi, Peoples R China
[3] Chengdu Med Coll, Sch Clin Med, Chengdu, Peoples R China
[4] Chengdu Med Coll, Sch Basic Med, Chengdu, Peoples R China
基金
中国国家自然科学基金;
关键词
Prostaglandin E-2; Lateral parabrachial nucleus; Fever; Lipopolysaccharide; Firing activity; RECEPTOR MESSENGER-RNA; VASCULOSUM-LAMINAE-TERMINALIS; BROWN ADIPOSE-TISSUE; PREOPTIC AREA; INDUCIBLE CYCLOOXYGENASE; THERMOSENSORY PATHWAY; EXPRESSING NEURONS; FOS EXPRESSION; SOLITARY TRACT; CELL GROUPS;
D O I
10.1159/000518491
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: The lateral parabrachial nucleus (LPBN) is considered to be a brain site of the pyrogenic action of prostaglandin (PG) E-2 outside of the preoptic area. Yet, the role of the LPBN in fever following a systemic immune challenge remains poorly understood. Methods: We examined the expression of cyclooxygenase-2 (COX-2) and microsomal PGE synthase-1 (mPGES-1) in the LPBN after the intraperitoneal injection of lipopolysaccharide (LPS). We investigated the effects of LPBN NS-398 (COX-2 inhibitor) on LPS-induced fever, the effects of direct LPBN PGE(2) administration on the energy expenditure (EE), brown adipose tissue (BAT) thermogenesis, neck muscle electromyographic activity and tail temperature, and the effects of PGE(2) on the spontaneous firing activity and thermosensitivity of in vitro LPBN neurons in a brain slice. Results: The COX-2 and mPGES-1 enzymes were upregulated at both mRNA and protein levels. The microinjection of NS-398 in the LPBN attenuated the LPS-induced fever. Direct PGE(2) administration in the LPBN resulted in a febrile response by a coordinated response of increased EE, BAT thermogenesis, shivering, and possibly decreased heat loss through the tail. The LPBN neurons showed a clear anatomical distinction in the firing rate response to PGE(2), with the majority of PGE(2)-excited or -inhibited neurons being located in the external lateral or dorsal subnucleus of the LPBN, respectively. However, neither the firing rate nor the thermal coefficient response to PGE(2) showed any difference between warm-sensitive, cold-sensitive, and temperature-insensitive neurons in the LPBN. Conclusions: PGE(2) synthesized in the LPBN was at least partially involved in LPS-induced fever via its different modulations of the firing rate of neurons in different LPBN subnuclei. (c) 2021 S. Karger AG, Basel
引用
收藏
页码:399 / 416
页数:18
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