GABA‐Mediated Synaptic Interaction Between the Visual and Vestibular Pathways of Hermissenda

Abstract: The synaptic convergence of the eyes and the vestibular hair cells in the nudibranch mollusc Hermissenda has been shown previously to mediate the learning of simple visual‐vestibular associations. The neurotransmitter mediating this interaction between the visual and vestibular organs was characterized. HPLC chromatography, confirmed by mass spectroscopic analysis, demonstrated endogenous GABA in the statocysts, in a concentration approximately 150 times greater than in the whole CMS. Additional confirmation was provided by immunocytochemical localization of GABA in hair cell axons and branches that converge with photoreceptor terminal branches. Depolarization of the hair cells in the caudal region of the statocyst in response to positive current injection or vibratory stimulation caused a hyperpolarization and a cessation of the type B photoreceptor impulse activity. The inhibition of the B cell was unaffected by addition to the artificial sea water bath of the adrenergic antagonist yohimbine (250 μM), the cholinergic antagonist atropine (250 μM), and the serotonergic antagonist imipramine (50 μM). In contrast, the GABAA antagonist bicuculline (250 μM) significantly reduced the inhibitory interaction. Moreover, the GABA reuptake inhibitor guvisine (250 μM)M) increased the hyperpolarization. Pressure microapplication of GABA (12.5 or 25 μM) onto the terminal branches of the B cell resulted in a concentration‐dependent hyperpolarization and cessation of spikes in the B cell. Depolarization of the caudal hair cell, or direct GABA application, decreased input resistance across the B cell soma membrane. Moreover, removal of chloride from the extracellular solution reduced inhibition of the B cell induced by GABA application or hair cell stimulation. Furthermore, application of the GABAB agonist baclofen hyperpolarized the type B cell and reduced or eliminated spontaneous impulse activity at the resting membrane potential. The reversal potentials for inhibition induced in all three procedures ranged from −70 to −80 mV and were consistent with mixed Cl‐ and K+ conductances. These results implicate GABA as the endogenous neurotransmitter mediating visual‐vestibular interactions in this animal, and suggest a possible role of GABA in visual‐vestibular associative learning.

[1]  N. Osborne,et al.  Distribution of GABA and other amino acids in different tissues of the gastropod mollusc Helix pomatia, including in vitro experiments with 14 C glucose and 14 C glutamic acid. , 1971, The International journal of neuroscience.

[2]  B. Yamamoto,et al.  An improved and rapid HPLC-EC method for the isocratic separation of amino acid neurotransmitters from brain tissue and microdialysis perfusates. , 1988, Life sciences.

[3]  D. Carpenter,et al.  Receptors for gamma-aminobutyric acid (GABA) on aplysia neurons , 1978, Brain Research.

[4]  D L Alkon,et al.  Ultrastructure of photoreceptors in the eye ofHermissenda labelled with intracellular injections of horseradish peroxidase , 1979, Journal of neurocytology.

[5]  D. Alkon,et al.  Optical sectioning of HRP-stained molluscan neurons , 1982, Journal of Neuroscience Methods.

[6]  D. Sattelle,et al.  Ionic events following GABA receptor activation in an identified insect motor neuron , 1988, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[7]  B. Yamamoto,et al.  A rapid and simple HPLC microassay for biogenic amines in discrete brain regions , 1988, Pharmacology Biochemistry and Behavior.

[8]  W. Paton Central and synaptic transmission in the nervous system; pharmacological aspects. , 1958, Annual review of physiology.

[9]  D. Alkon,et al.  Positive synaptic feedback in visual system of nudibranch mollusk Hermissenda crassicornis. , 1982, Journal of neurophysiology.

[10]  N. Satoh,et al.  Monoclonal antibodies against components of the myoplasm of eggs of the ascidian Ciona intestinalis partially block the development of muscle-specific acetylcholinesterase. , 1987, Development.

[11]  D. Alkon,et al.  Cholinergic features of photoreceptor synapses in Hermissenda. , 1979, Journal of neurophysiology.

[12]  J. Farley,et al.  Neurochemical and immunocytochemical studies of serotonin in thehermissenda central nervous system , 1989, Brain Research Bulletin.

[13]  D L Alkon,et al.  Memory storage and neural systems. , 1989, Scientific American.

[14]  D. L. Alkon,et al.  Membrane depolarization accumulates during acquisition of an associative behavioral change. , 1980, Science.

[15]  D. Alkon,et al.  Hair Cell Generator Potentials , 1973, The Journal of general physiology.

[16]  J. Nathans The genes for color vision. , 1989, Scientific American.

[17]  Daniel L. Alkon,et al.  Memory Traces in the Brain , 1987 .

[18]  D. Alkon Responses of hair cells to statocyst rotation , 1975, The Journal of general physiology.

[19]  N. Akaike,et al.  GABA-induced chloride current in rat isolated Purkinje cells. , 1989, The American journal of physiology.

[20]  M. Karnovsky,et al.  CYTOCHEMICAL DEMONSTRATION OF PEROXIDASE ACTIVITY WITH 3-AMINO-9-ETHYLCARBAZOLE , 1965, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[21]  D. Alkon,et al.  GABA-induced potentiation of neuronal excitability occurs during contiguous pairings with intracellular calcium elevation , 1991, Brain Research.

[22]  R. Wong,et al.  GABAA-receptor function in hippocampal cells is maintained by phosphorylation factors. , 1988, Science.

[23]  H. Steedman Ester Wax 1960: A Histological Embedding Medium , 1960 .

[24]  R. Mccaman,et al.  Gamma‐aminobutyric acid in ganglia and in single neurons from Aplysia and lobster , 1979, Journal of neurochemistry.

[25]  T. Crow Cellular and molecular analysis of associative learning and memory in Hermissenda , 1988, Trends in Neurosciences.

[26]  D. Alkon,et al.  Classical conditioning of Hermissenda: origin of a new response , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[27]  D. Alkon,et al.  An infraciliary network in statocyst hair cells , 1981, Journal of neurocytology.

[28]  D. Alkon,et al.  In vitro associative conditioning of Hermissenda: cumulative depolarization of type B photoreceptors and short-term associative behavioral changes. , 1987, Journal of neurophysiology.