Dissociated histaminergic neuron cultures from the tuberomammillary nucleus of rats: culture methods and ghrelin effects

被引:18
作者
Bajic, D
Hoang, QV
Nakajima, S
Nakajima, Y
机构
[1] Univ Illinois, Coll Med, Dept Anat & Cell Biol, Chicago, IL 60612 USA
[2] Univ Illinois, Coll Med, Dept Pharmacol, Chicago, IL 60612 USA
基金
美国国家卫生研究院;
关键词
adenosine deaminase; appetite; electrophysiology; GIRK; Kir3; nociceptin; obesity;
D O I
10.1016/j.jneumeth.2003.09.008
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The tuberomammillary nucleus (TMN) in the hypothalamus is the sole source of histamine in the brain. This nucleus, by innervating various brain regions, plays an important role for vital functions such as arousal and appetite. We have developed dissociated primary histaminergic neuron cultures from TMN of postnatal (3 and 10-day-old) rats. More than 50% of our cultured neurons from the TMN were histaminergic as revealed by adenosine deaminase (AD) as well as histamine immunocytochemistry. Among large neurons (diameter, >22 mum), more than 88% were histaminergic. Such large neurons (mean diameter, 26.5 mum) were used for electrophysiology. Using about 2-month-old TMN cultures, we investigated the effects of ghrelin, a recently discovered appetite-stimulating endogenous peptide. In GTPgammaS-loaded neurons, ghrelin (3 muM) suppressed currents that had previously been activated by an inhibitory neuropeptide, nociceptin. The mean current suppression by ghrelin was 471 +/- 128 pA (S.E.M., n = 7). The I-V relationship revealed that the ghrelin-suppressed current was inwardly rectifying with a reversal potential around E-K. These results suggest that ghrelin inhibits G protein-coupled inward rectifier K+ channels (Kir3, GIRK) of TMN neurons and that our TMN cultures are useful for investigating physiological properties of brain histaminergic neurons. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:177 / 184
页数:8
相关论文
共 36 条
[1]  
Bajic D, 2003, BIOPHYS J, V84, p395A
[2]  
BAUGHMAN RW, 1991, CULTURING NERVE CELL, P227
[3]   A METHOD FOR DEFINED SECTIONING OF FRESH YOUNG BRAINS AND COLLECTION OF SMALL REGIONS FOR CELL AND TISSUE-CULTURE [J].
BUSE, E ;
MATTHAEI, H .
JOURNAL OF NEUROSCIENCE METHODS, 1983, 7 (04) :377-387
[4]   Narcolepsy in orexin knockout mice:: Molecular genetics of sleep regulation [J].
Chemelli, RM ;
Willie, JT ;
Sinton, CM ;
Elmquist, JK ;
Scammell, T ;
Lee, C ;
Richardson, JA ;
Williams, SC ;
Xiong, YM ;
Kisanuki, Y ;
Fitch, TE ;
Nakazato, M ;
Hammer, RE ;
Saper, CB ;
Yanagisawa, M .
CELL, 1999, 98 (04) :437-451
[5]   The distribution and mechanism of action of ghrelin in the CNS demonstrates a novel hypothalamic circuit regulating energy homeostasis [J].
Cowley, MA ;
Smith, RG ;
Diano, S ;
Tschöp, M ;
Pronchuk, N ;
Grove, KL ;
Strasburger, CJ ;
Bidlingmaier, M ;
Esterman, M ;
Heiman, ML ;
Garcia-Segura, LM ;
Nillni, EA ;
Mendez, P ;
Low, MJ ;
Sotonyi, P ;
Friedman, JM ;
Liu, HY ;
Pinto, S ;
Colmers, WF ;
Cone, RD ;
Horvath, TL .
NEURON, 2003, 37 (04) :649-661
[6]   The hypocretins: Hypothalamus-specific peptides with neuroexcitatory activity [J].
De Lecea, L ;
Kilduff, TS ;
Peyron, C ;
Gao, XB ;
Foye, PE ;
Danielson, PE ;
Fukuhara, C ;
Battenberg, ELF ;
Gautvik, VT ;
Bartlett, FS ;
Frankel, WN ;
van den Pol, AN ;
Bloom, FE ;
Gautvik, KM ;
Sutcliffe, JG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (01) :322-327
[7]   Opposite modulation of histaminergic neurons by nociceptin and morphine [J].
Eriksson, KS ;
Stevens, DR ;
Haas, HL .
NEUROPHARMACOLOGY, 2000, 39 (12) :2492-2498
[8]   Distribution of mRNA encoding the growth hormone secretagogue receptor in brain and peripheral tissues [J].
Guan, XM ;
Yu, H ;
Palyha, OC ;
McKee, KK ;
Feighner, SD ;
Sirinathsinghji, DJS ;
Smith, RG ;
VanderPloeg, LHT ;
Howard, AD .
MOLECULAR BRAIN RESEARCH, 1997, 48 (01) :23-29
[9]  
HAAS HL, 1988, J PHYSIOL-LONDON, V399, P633
[10]   HISTAMINE AND NORADRENALINE DECREASE CALCIUM-ACTIVATED POTASSIUM CONDUCTANCE IN HIPPOCAMPAL PYRAMIDAL CELLS [J].
HAAS, HL ;
KONNERTH, A .
NATURE, 1983, 302 (5907) :432-434