Effects of variance in mini amplitude on stimulus-evoked release: A comparison of two models

被引:31
|
作者
Frerking, M [1 ]
Wilson, M [1 ]
机构
[1] UNIV CALIF DAVIS,SECT NEUROBIOL PHYSIOL & BEHAV,DIV BIOL SCI,DAVIS,CA 95616
关键词
D O I
10.1016/S0006-3495(96)79774-6
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The strength of synaptic connections between two neurons is characterized by the number of release sites (N) on the presynaptic cell, the probability (p) of transmitter release at those sites in response to a stimulus, and the average size (A) of the postsynaptic response from each site. Quantal analysis can determine N, p, and A, but the large variance in the amplitudes of minis at central synapses is predicted to obscure quantal peaks and render quantal analysis unusable. Recently it has been suggested that the variance in mini amplitude is generated by differences between release sites, rather than by quantum-to-quantum fluctuations at identical sites, and that this form of variance in mini amplitude reduces the amount of variance expected in quantal peaks. Using simulations, we examine the possibility of resolving quantal peaks assuming either form of variance in mini amplitude. We find that individual quantal peaks are resolvable in neither case, provided that the uniquantal distribution is similar to the mini distribution. Because this lack of resolution compromises the utility of quantal analysis, we develop a general description that can solve N and p, given the statistical parameters of the mini distribution and the evoked distribution. We find that this description is relatively insensitive to the source of variance in mini amplitude.
引用
收藏
页码:2078 / 2091
页数:14
相关论文
共 50 条
  • [1] Stimulus-evoked synchronization in neuronal models
    Li, GB
    Feng, JF
    [J]. COMPUTATIONAL NEUROSCIENCE: TRENDS IN RESEARCH 2004, 2004, : 203 - 208
  • [2] Stimulus-evoked synchronization in neuronal models
    Li, GB
    Feng, HF
    [J]. NEUROCOMPUTING, 2004, 58 : 203 - 208
  • [3] NALOXONE PROMOTES STIMULUS-EVOKED VASOPRESSIN RELEASE INVIVO
    KNEPEL, W
    NUTTO, D
    ANHUT, H
    HERTTING, G
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1980, 65 (04) : 449 - 450
  • [4] COMPARISON OF RESTING AND STIMULUS-EVOKED CATECHOLAMINE RELEASE FROM THE FEMORAL AND RENAL VASCULAR BEDS OF THE DOG
    PETROVIC, T
    HARRIS, PJ
    BELL, C
    [J]. JOURNAL OF THE AUTONOMIC NERVOUS SYSTEM, 1988, 25 (2-3): : 195 - 203
  • [5] Stimulus-evoked glutamate release is diminished by acute exposure to uranium in vitro
    Vietti, Kimberly R. N.
    Lasley, Stephen M.
    [J]. NEUROTOXICOLOGY AND TERATOLOGY, 2007, 29 (06) : 607 - 612
  • [6] Time-dependent assessment of stimulus-evoked regional dopamine release
    Lippert, Rachel N.
    Cremer, Anna Lena
    Thanarajah, Sharmili Edwin
    Korn, Clio
    Jahans-Price, Thomas
    Burgeno, Lauren M.
    Tittgemeyer, Marc
    Bruening, Jens C.
    Walton, Mark E.
    Backes, Heiko
    [J]. NATURE COMMUNICATIONS, 2019, 10 (1)
  • [7] THE IMPLICATION OF STIMULUS-EVOKED ATP RELEASE FROM NEURONAL AND EXTRANEURONAL SITES
    KATSURAGI, T
    FURUKAWA, T
    [J]. FOLIA PHARMACOLOGICA JAPONICA, 1991, 98 (03) : 227 - 234
  • [8] Time-dependent assessment of stimulus-evoked regional dopamine release
    Rachel N. Lippert
    Anna Lena Cremer
    Sharmili Edwin Thanarajah
    Clio Korn
    Thomas Jahans-Price
    Lauren M. Burgeno
    Marc Tittgemeyer
    Jens C. Brüning
    Mark E. Walton
    Heiko Backes
    [J]. Nature Communications, 10
  • [9] EFFECTS OF OPIOIDS ON THE HEAT STIMULUS-EVOKED SUBSTANCE-P RELEASE AND THERMAL EDEMA IN THE RAT HIND PAW
    YONEHARA, N
    IMAI, Y
    INOKI, R
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1988, 151 (03) : 381 - 387
  • [10] THE SUPPRESSION OF STIMULUS-EVOKED RELEASE OF AMINO-ACID NEUROTRANSMITTERS FROM SYNAPTOSOMES BY VERAPAMIL
    NORRIS, PJ
    DHALIWAL, DK
    DRUCE, DP
    BRADFORD, HF
    [J]. JOURNAL OF NEUROCHEMISTRY, 1983, 40 (02) : 514 - 521