Presynaptic inhibitory effect of acetylcholine in the hippocampus

(1) In order to investigate the effects of acetylcholine (ACh) on synaptic transmission in the rat hippocampus, extracellular and intracellular recordings were made from pyramidal neurons in an in vitro slice preparation while synaptic inputs to the cell population were stimulated. ACh was applied ionophoretically into somatic and dendritic layers of the slice. (2) ACh applied into the apical dendritic layer of the CA1 region reduced the size of the locally evoked field excitatory postsynaptic potential (EPSP) without altering the size of the afferent fiber volley. Likewise, dendritically applied ACh reduced the size of intracellularly recorded EPSPs. This effect of ACh appeared to be muscarinic since it was not affected by hexamethonium (up to 3 X 10–5 M) but was antagonized by atropine in a dose-dependent manner. (3) The distribution of Ach-sensitive sites matched closely the spatial distribution of activated synapses on the pyramidal cell dendrites as shown by ionophoretic mapping experiments. (4) In contrast to the effects of dendritic applications of ACh, ionophoresis of ACh into the cell layer resulted in an increase and prolongation of EPSPs and a transient decrease in the size of recurrent somatic inhibitory postsynaptic potentials (IPSPs). These effects on synaptic potentials could not be explained by the observed changes in membrane potential and input resistance following somatic application of ACh. (5) Short dendritic applications of ACh had no consistent effect on the membrane potential or slope conductance of pyramidal neurons and did not attenuate the depolarization evoked by brief dendritic applications of glutamate. In addition, the time course of ACh-reduced EPSPs was not different from control. (6) We conclude that ACh exerts a presynaptic inhibitory effect on both excitatory and inhibitory afferents to hippocampal pyramidal neurons. This effect of ACh is widespread, occurring in all regions of Ammon's horn tested as well as in stratum moleculare of fascia dentata.

[1]  Karl Frank,et al.  Basic Mechanisms of Synaptic Transmission in the Central Nervous System , 1959 .

[2]  Activation of the dentate area by septal stimulation. , 1961, Acta physiologica Scandinavica.

[3]  P. Andersen,et al.  Activation of the field CA-1 of the hippocampus by septal stimulation. , 1961, Acta physiologica Scandinavica.

[4]  T. Blackstad,et al.  An electron microscopic study of the stratum radiatum of the rat hippocampus (regio superior, CA 1) with particular emphasis on synaptology , 1962, The Journal of comparative neurology.

[5]  E. Gray A Morphological Basis for Pre-synaptic Inhibition? , 1962, Nature.

[6]  T. Blackstad Ultrastructural Studies on the Hippocampal Region , 1963 .

[7]  C. Stumpf,et al.  Drug action on the electrical activity of the hippocampus. , 1965, International review of neurobiology.

[8]  T. Biscoe,et al.  Micro‐electrophoretic studies of neurones in the cat hippocampus , 1966, The Journal of physiology.

[9]  C. Stefanis,et al.  A critique of iontophoretic studies of central nervous system neurons. , 1967, International review of neurobiology.

[10]  C Yamamoto,et al.  Presynaptic action of acetylcholine in thin sections from the guinea pig dentate gyrus in vitro. , 1967, Experimental neurology.

[11]  R. Eisenberg,et al.  The interpretation of current-voltage relations recorded from a spherical cell with a single microelectrode. , 1972, Biophysical journal.

[12]  B. Srebro,et al.  Changes in acetylcholinesterase and distribution of degenerating fibres in the hippocampal region after septal lesions in the rat. , 1973, Brain research.

[13]  G. Lynch,et al.  The distribution of septal projections to the hippocampus of the rat , 1973, The Journal of comparative neurology.

[14]  J. Phillis,et al.  Acetylcholine sensitivity of hippocampal formation neurons. , 1974, Canadian journal of physiology and pharmacology.

[15]  S. Landis,et al.  Afferents to the hippocampus of the rat studied with the method of retrograde transport of horseradish peroxidase. , 1974, Brain research.

[16]  G. Aghajanian,et al.  Denervation supersensitivity in the cholinergic septo-hippocampal pathway: A microiontophoretic study , 1975, Brain Research.

[17]  Proceedings: Influences of the septum on the hippocampal dentate area which are unaccompanied by field potentials. , 1975, The Journal of physiology.

[18]  Avarez-Leefmans Fj,et al.  Proceedings: Influences of the septum on the hippocampal dentate area which are unaccompanied by field potentials. , 1975 .

[19]  J. D. Dudar The effect of septal nuclei stimulation on the release of acetylcholine from the rabbit hippocampus , 1975, Brain Research.

[20]  H. Fibiger,et al.  Analysis of the septo-hippocampal pathway by light and electron microscopic autoradiography , 1976, Brain Research.

[21]  L. Swanson The anatomical organization of septo-hippocampal projections. , 1977, Ciba Foundation symposium.

[22]  J. Marchand,et al.  Cholinergic mechanisms and short-term potentiation. , 1977, Ciba Foundation symposium.

[23]  M. Segal The acetylcholine receptor in the rat hippocampus; nicotinic, muscarinic or both? , 1978, Neuropharmacology.

[24]  P. Andersen,et al.  Functional characteristics of unmyelinated fibres in the hippocampal cortex , 1978, Brain Research.

[25]  Inhibition produced by iontophoretically applied acetylcholine in area CA1 of thin hippocampal slices from the rat. , 1978, Acta physiologica Scandinavica.

[26]  Jørn Hounsgaard,et al.  Presynaptic inhibitory action of acetylcholine in area CA1 of the hippocampus , 1978, Experimental Neurology.

[27]  H Wachtel,et al.  Prolonged inhibition in burst firing neurons: synaptic inactivation of the slow regenerative inward current. , 1978, Science.

[28]  R K Wong,et al.  Dendritic mechanisms underlying penicillin-induced epileptiform activity. , 1979, Science.

[29]  P. Andersen,et al.  Septo-hippocampal pathway necessary for dentate theta production , 1979, Brain Research.

[30]  G. Fischbach,et al.  Enkephalin inhibits release of substance P from sensory neurons in culture and decreases action potential duration. , 1979, Proceedings of the National Academy of Sciences of the United States of America.

[31]  R. Dingledine,et al.  Penicillin blocks hippocampal IPSPs, unmasking prolonged EPSPs , 1979, Brain Research.

[32]  R. Dingledine,et al.  Acetylcholine as an excitatory and inhibitory transmitter in the mammalian central nervous system. , 1979, Progress in brain research.

[33]  R. Dingledine,et al.  Reduced inhibition during epileptiform activity in the in vitro hippocampal slice. , 1980, The Journal of physiology.

[34]  R. Dingledine,et al.  The in vitro brain slice as a useful neurophysiological preparation for intracellular recording , 1980, Journal of Neuroscience Methods.

[35]  R. Dingledine,et al.  Conductance changes and inhibitory actions of hippocampal recurrent IPSPs , 1980, Brain Research.

[36]  J. Fleshman,et al.  Effect of presynaptic inhibition on axonal potentials, terminal potentials, focal synaptic potentials, and EPSPs in cat spinal cord. , 1980, Journal of neurophysiology.

[37]  R. Dingledine,et al.  The excitatory action of acetylcholine on hippocampal neurones of the guinea pig and rat maintained in vitro , 1981, Brain Research.

[38]  G. Somjen,et al.  Calcium dependance of synaptic transmission in the hippocampal slice , 1981, Brain Research.