Selective histamine H3 receptor antagonists for treatment of cognitive deficiencies and other disorders of the central nervous system

被引:140
作者
Witkin, JM [1 ]
Nelson, DL [1 ]
机构
[1] Eli Lilly & Co, Lilly Corp Ctr, Lilly Res Labs, Neurosci Discovery Res, Indianapolis, IN 46285 USA
关键词
histamine; H-3; receptors; cognition; attention deficit hyperactivity disorder; schizophrenia; review;
D O I
10.1016/j.pharmthera.2004.05.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Evidence exists to implicate the monoamine histamine in the control of arousal and cognitive functions. Antagonists of H-3 receptors are postsynaptic and presynaptic modulators of neural transmission in a variety of neuronal circuits relevant to cognition. Accumulating neuroanatomical, neurochemical, pharmacological, and behavioral data support the idea that H-3 receptor antagonists may function to improve cognitive performances in disease states (e.g., Alzheimer's disease and mild cognitive impairment states). Thus, H-3 receptor antagonists have been shown to increase performance in attention and memory tests in nonhuman experiments and prevent the degradation in performances produced by scopolamine, NIK-801, or age. In contrast, agonists of the H-3 receptor generally produce cognitive impairing effects in animal models. The role of H-3 receptors in these behavioral effects is substantiated by data indicating a central origin for their effects, the selectivity of some of the H-3 receptor antagonists studied, and the pharmacological modification of effects of H-3 receptor antagonists by selective H-3 receptor agonists. Data and issues that challenge the potential role for H-3 receptor antagonists in cognitive processes are also critically reviewed. H-3 receptor antagonists may also have therapeutic value in the management of obesity, pain, sleep disorders, schizophrenia, and attention deficit hyperactivity disorder. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:1 / 20
页数:20
相关论文
共 162 条
[41]   NEUROBIOLOGICAL FEATURES COMMON TO MEMORY MODULATION BY MANY TREATMENTS [J].
GOLD, PE .
ANIMAL LEARNING & BEHAVIOR, 1989, 17 (01) :94-100
[42]  
GREEN JP, 1964, FED PROC, V23, P1095
[43]   The role of histamine and the tuberomamillary nucleus in the nervous system [J].
Haas, H ;
Panula, P .
NATURE REVIEWS NEUROSCIENCE, 2003, 4 (02) :121-130
[44]   Nicotine-induced enhancement of attention in the five-choice serial reaction time task: the influence of task demands [J].
Hahn, B ;
Shoaib, M ;
Stolerman, IP .
PSYCHOPHARMACOLOGY, 2002, 162 (02) :129-137
[45]   Antiobesity effects of A-331440, a novel non-imidazole histamine H3 receptor antagonist [J].
Hancock, AA ;
Bennani, YL ;
Bush, EN ;
Esbenshade, TA ;
Faghih, R ;
Fox, GB ;
Jacobson, P ;
Knourek-Segel, V ;
Krueger, KM ;
Nuss, ME ;
Pan, JB ;
Shapiro, R ;
Witte, DG ;
Yao, BB .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2004, 487 (1-3) :183-197
[46]   Genetic and pharmacological aspects of histamine H3 receptor heterogeneity [J].
Hancock, AA ;
Esbenshade, TA ;
Krueger, KM ;
Yao, BB .
LIFE SCIENCES, 2003, 73 (24) :3043-3072
[47]  
Hill SJ, 1997, PHARMACOL REV, V49, P253
[48]   ALPHA-2-ADRENOCEPTOR-MEDIATED INHIBITION OF HISTAMINE-RELEASE FROM RAT CEREBRAL CORTICAL SLICES [J].
HILL, SJ ;
STRAW, RM .
BRITISH JOURNAL OF PHARMACOLOGY, 1988, 95 (04) :1213-1219
[49]   Effect of the histamine H3-antagonist clobenpropit on spatial memory deficits induced by MK-801 as evaluated by radial maze in Sprague-Dawley rats [J].
Huang, YW ;
Hu, WW ;
Chen, Z ;
Zhang, LS ;
Shen, HQ ;
Timmerman, H ;
Leurs, R ;
Yanai, K .
BEHAVIOURAL BRAIN RESEARCH, 2004, 151 (1-2) :287-293
[50]   Arousal effect of orexin A depends on activation of hte histmic system [J].
Huang, ZL ;
Qu, WM ;
Li, WD ;
Mochizuki, T ;
Eguchi, N ;
Watanabe, T ;
Urade, Y ;
Hayaishi, O .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (17) :9965-9970