Expression of the leptin receptor in rat and human nodose ganglion neurones

被引:99
作者
Burdyga, G
Spiller, D
Morris, R
Lal, S
Thompson, DG
Saeed, S
Dimaline, R
Varro, A
Dockray, GJ
机构
[1] Univ Liverpool, Physiol Lab, Liverpool L69 3BX, Merseyside, England
[2] Univ Liverpool, Sch Biol Sci, Liverpool L69 3BX, Merseyside, England
[3] Univ Liverpool, Dept Vet Sci, Liverpool L69 3BX, Merseyside, England
[4] Hope Hosp, Div Gastroenterol, Salford M6 8HD, Lancs, England
[5] Hope Hosp, Directorate ENT Surg, Salford M6 8HD, Lancs, England
基金
英国生物技术与生命科学研究理事会;
关键词
cholecystokinin; vagal afferent neurones; cocaine- and amphetamine-related transcript; cholecystokinin type A receptor; satiety;
D O I
10.1016/S0306-4522(01)00474-2
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
There is evidence for interactions between leptin and cholecystokinin in controlling food intake. Since cholecystokinin acts on vagal afferent neurones, we asked whether the leptin receptor was also expressed by these neurones. Primers for different forms of the leptin receptor were used in reverse transcriptase-polymerase chain reaction (RT-PCR) of rat and human nodose ganglia. RT-PCR yielded products corresponding to the long (functional) form as well as short forms of the rat leptin receptor. Moreover, RT-PCR revealed the long form of the leptin receptor in a human nodose ganglion. The identities of RT-PCR products were confirmed by sequencing. Primers corresponding to leptin itself did not give RT-PCR products in nodose ganglia, Immunocytochemical studies revealed leptin-receptor immunoreactivity in neuronal cell bodies, Many neurones co-expressed the leptin and cholecystokinin type A receptors, or leptin receptor and cocaine- and amphetamine-related transcript. We conclude that vagal afferent neurones that express the cholecystokinin type A receptor and cocaine- and amphetamine-related transcript, may also express the long form of the leptin receptor providing a neurochemical basis for observations of interactions between cholecystokinin and leptin. (C) 2002 IBRO. Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:339 / 347
页数:9
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