Plasticity of synaptic transmission in autonomic ganglia

被引:52
作者
Alkadhi, KA [1 ]
Alzoubi, KH [1 ]
Aleisa, AM [1 ]
机构
[1] Univ Houston, Dept Pharmacol & Pharmaceut Sci, Houston, TX 77204 USA
关键词
D O I
10.1016/j.pneurobio.2005.02.002
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Synaptic plasticity is a term that describes long-lasting changes in the efficacy of synaptic transmission resulting from certain patterned activities of the presynaptic nerve. One form of synaptic plasticity, long-term potentiation (UP), is an activity-dependent marked increase in synaptic efficacy that has been extensively studied in various regions of the central nervous system, particularly the hippocampus, where UP is widely believed to be a cellular correlate of learning and memory. A similar phenomenon has been identified in sympathetic ganglia even before Bliss and Lomo coined the term UP in 1973. Ganglionic UP (gLTP) of the nicotinic pathway is a similarly long-lasting increase in synaptic effectiveness that can be induced in ganglia following a brief train of relatively high frequency stimulation (HFS) of the preganglionic nerve. Remarkably similar to the UP of the hippocampus, gLTP has been demonstrated in autonomic ganglia from a number of vertebrates including mammalian, amphibian and avian species. Several other forms of long-lasting increases in synaptic effectiveness have been demonstrated in sympathetic ganglia following exposure to adrenergic agonists, neuroactive peptides and cyclic nucleotides and even after a challenge by an antigen. The main emphasis of this review, however, will be on the activity-dependent gLTP of the mammalian sympathetic ganglia, in particular the superior cervical ganglion of the rat. Since the last, excellent and comprehensive review of this ganglionic function by Briggs in 1995, important discoveries about the mechanisms of induction and maintenance of gLTP have been reported, including the finding that the response is uniquely dependent on serotonin for both the induction phase and maintenance phase. These new advances will be discussed in depth in this review. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:83 / 108
页数:26
相关论文
共 277 条
  • [1] ACTIONS OF GAMMA-AMINOBUTYRIC ACID ON SYMPATHETIC-GANGLION CELLS
    ADAMS, PR
    BROWN, DA
    BROWN, DA
    SAUNDERS, L
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 1975, 250 (01): : 85 - 120
  • [2] Alterations in sympathetic ganglionic transmission in response to angiotensin II in (mRen2)27 transgenic rats
    Aileru, AA
    Logan, E
    Callahan, M
    Ferrario, CM
    Ganten, D
    Diz, DI
    [J]. HYPERTENSION, 2004, 43 (02) : 270 - 275
  • [3] Synaptic plasticity in sympathetic ganglia from acquired and inherited forms of ouabain-dependent hypertension
    Aileru, AA
    De Albuquerque, A
    Hamlyn, JM
    Manunta, P
    Shah, JR
    Hamilton, MJ
    Weinreich, D
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2001, 281 (02) : R635 - R644
  • [4] Role of mast cell- and non-mast cell-derived inflammatory mediators in immunologic induction of synaptic plasticity
    Albuquerque, AAC
    LealCardoso, JH
    Weinreich, D
    [J]. BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH, 1997, 30 (07) : 909 - 912
  • [5] ALKADHI KA, 1993, ARCH INT PHARMACOD T, V322, P66
  • [6] A COMPARATIVE-STUDY OF THE ACTIONS OF HISTAMINE-H2 RECEPTOR ANTAGONISTS ON TRANSMISSION IN THE ISOLATED SUPERIOR CERVICAL-GANGLION OF THE RAT
    ALKADHI, KA
    BASSEY, EI
    HOGAN, YH
    [J]. NEUROPHARMACOLOGY, 1990, 29 (03) : 285 - 290
  • [7] EFFECTS OF 1-METHYL-4-PHENYL-1,2,3,6-TETRAHYDROXYPYRIDINE (MPTP) ON GANGLIONIC TRANSMISSION
    ALKADHI, KA
    HOGAN, YH
    [J]. JOURNAL OF AUTONOMIC PHARMACOLOGY, 1992, 12 (01): : 15 - 23
  • [8] ALKADHI KA, 1986, J PHARMACOL EXP THER, V238, P547
  • [9] Alkadhi KA, 1998, N-S ARCH PHARMACOL, V358, pR265
  • [10] Inhibition of ganglionic long-term potentiation decreases blood pressure in spontaneously hypertensive rats
    Alkadhi, KA
    Otoom, SA
    Tanner, FL
    Sockwell, D
    Hogan, YH
    [J]. EXPERIMENTAL BIOLOGY AND MEDICINE, 2001, 226 (11) : 1024 - 1030