SYNAPTIC ARCHITECTURE OF GLOMERULI IN SUPERFICIAL DORSAL HORN OF RAT SPINAL-CORD, AS SHOWN IN SERIAL RECONSTRUCTIONS
SYNAPTIC ARCHITECTURE OF GLOMERULI IN SUPERFICIAL DORSAL HORN OF RAT SPINAL-CORD, AS SHOWN IN SERIAL RECONSTRUCTIONS
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DOI:
10.1007/bf01258448
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发表时间:
1985-01-01
期刊:
影响因子:
--
通讯作者:
COIMBRA, A
中科院分区:
文献类型:
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作者:
RIBEIRODASILVA, A;PIGNATELLI, D;COIMBRA, A
Using serial section EM analysis, synaptic organization of glomeruli in lamina II of the dorsal horn of the rat was examined. Four C1-terminals (small, dark and sinuous), 4 CIIa (large, light and regular, without neurofilaments) and 4 CIIb (with neurofilaments) at the centers of synaptic glomeruli of types I, IIa and IIb, respectively, were serially sectioned and reconstructed. Asymmetrical synapses between the central terminal (C) and dendritic profiles without synaptic vesicles (D) prevailed in all types of glomeruli. Symmetrical dendroaxonic contacts with presynaptic dendrites (V1 .fwdarw. C) occurred practically only in type 1 glomeruli in which there were also more asymmetrical C .fwdarw. V1 contacts than in type II glomeruli. Symmetrical axoaxonic synapses V2 .fwdarw. C were more abundant in type IIa and IIb glomeruli. Type IIa glomeruli had a significantly larger number of C .fwdarw. D synapses and of all synapses per unit area of C surface, than type IIb glomeruli. Triadic systems with C and D postsynaptic to V2 were nearly as numerous as those involving V1 in type I glomeruli. Triads with V2 were largely preponderant in type IIa and virtually exclusive in type IIb. Each of the 3 types of glomerulus has its own pattern of synaptic interactions which might reflect specific complexes of feed-forward and feedback mechanisms. In type I glomeruli, excitation of 2nd-order neurons by nociceptive C1 terminals may be controlled in similar proportions by presynaptic dendrites excited without the glomerulus by the C terminal itself, or by peripheral axons excited from outside th8e glomerulus. This kind of control is likely to prevail in type IIa glomeruli and to be the only efficient modulatory mechanism in type IIb glomeruli.