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Synaptic connexions and related postsynaptic pharmacology studied in the cerebral ganglion of Aplysia.

作者信息

Hinzen D H, Davies M A

出版信息

Brain Res. 1978 Apr 7;144(1):49-62. doi: 10.1016/0006-8993(78)90434-1.

DOI:10.1016/0006-8993(78)90434-1
PMID:25121
Abstract

Interneuronal connexions have been studied within the cerebral ganglion of Aplysia californica. Excitatory monosynaptic connexions between two groups of cells located on the dorsal surface of the ganglion near the cerebropleural connectives were analyzed in detail. The monosynapticity of these connexions was established not only by the strict one-to-one correlation between presynaptic action potential and excitatory postsynaptic response (EPSP) and the constant latency for any given cell pair, but also by the following criteria: (a) gradual change in the EPSP following tetraethylammonium injection into the presynaptic neurone, (b) sustained EPSP in the presence of a high external calcium ion concentration, (c) sensitivity of the EPSP amplitude to presynaptic polarization. Iontophoretic application of acetylcholine, 5-hydroxytryptamine and glutamate on the postsynaptic cells elicited excitatory responses in many cases. Inhibitory responses were obtained by local iontophoresis of dopamine, gamma-aminobutyric acid and occasionally also by acetylcholine. The only agent found to block the EPSP was bufotenine, which also readily blocked the 5-hydroxytryptamine response. Bufotenine was completely ineffective on the acetylcholine or glutamate excitatory responses. Of the various cholinolytics tested, none had an effect on the EPSP. Our data all point to 5-hydroxytryptamine as a transmitter in the studied synaptic connexions. However, it must be emphasized that in the absence of biochemical and histological evidence the role of the 5-hydroxytryptamine cannot be regarded as conclusive.

摘要

相似文献

1
Synaptic connexions and related postsynaptic pharmacology studied in the cerebral ganglion of Aplysia.
Brain Res. 1978 Apr 7;144(1):49-62. doi: 10.1016/0006-8993(78)90434-1.
2
On the transmitter function of 5-hydroxytryptamine at excitatory and inhibitory monosynaptic junctions.5-羟色胺在兴奋性和抑制性单突触连接处的递质功能
J Physiol. 1974 Dec;243(2):457-81. doi: 10.1113/jphysiol.1974.sp010762.
3
Presynaptic inhibition and histamine in cerebral ganglion of Aplysia.海兔脑神经节中的突触前抑制与组胺
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Multiple interneuronal afferents to the giant cells in Aplysia.海兔巨细胞的多条中间神经元传入纤维。
J Physiol. 1975 May;247(2):299-319. doi: 10.1113/jphysiol.1975.sp010933.
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Excitatory amino acid neurotransmission at sensory-motor and interneuronal synapses of Aplysia californica.加州海兔感觉运动和中间神经元突触处的兴奋性氨基酸神经传递。
J Neurophysiol. 1993 Sep;70(3):1221-30. doi: 10.1152/jn.1993.70.3.1221.
6
Intra- and interganglionic synaptic connections in the CNS of Aplysia.海兔中枢神经系统内神经节间和神经节内的突触连接。
Brain Res Bull. 1979 May-Jun;4(3):393-406. doi: 10.1016/s0361-9230(79)80017-9.
7
Histamine and FLRFamide regulate acetylcholine release at an identified synapse in Aplysia in opposite ways.组胺和FLRFamide以相反的方式调节海兔特定突触处的乙酰胆碱释放。
J Physiol. 1990 Oct;429:147-68. doi: 10.1113/jphysiol.1990.sp018249.
8
Physiological and kinetic properties of cholinergic receptors activated by multiaction interneurons in buccal ganglia of Aplysia.海兔口腔神经节中多作用中间神经元激活的胆碱能受体的生理和动力学特性。
J Neurophysiol. 1977 Mar;40(2):333-48. doi: 10.1152/jn.1977.40.2.333.
9
The quantal release at a neuro-neuronal synapse is regulated by the content of acetylcholine in the presynaptic cell.神经-神经元突触处的量子释放受突触前细胞中乙酰胆碱含量的调节。
J Physiol (Paris). 1986;81(4):270-7.
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Development of post-tetanic potentiation at identified inhibitory and excitatory synapses in Aplysia.海兔中已确定的抑制性和兴奋性突触处强直后增强的发展。
J Physiol. 1982 Jan;322:223-40. doi: 10.1113/jphysiol.1982.sp014034.

引用本文的文献

1
Blocking action of intracellularly injected neuraminidase on central synapses in vivo.细胞内注射神经氨酸酶对体内中枢突触的阻断作用。
Pflugers Arch. 1980 May;385(1):45-50. doi: 10.1007/BF00583914.
2
Transmitter release: ruthenium red used to demonstrate a possible role of sialic acid containing substrates.递质释放:使用钌红来证明含唾液酸底物的可能作用。
J Physiol. 1979 Jun;291:161-78. doi: 10.1113/jphysiol.1979.sp012805.