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成年大鼠脊髓切片中胶状质神经元的盲法膜片钳记录:突触电流的药理学特性

Blind patch-clamp recordings from substantia gelatinosa neurons in adult rat spinal cord slices: pharmacological properties of synaptic currents.

作者信息

Yoshimura M, Nishi S

机构信息

Department of Physiology, Kurume University School of Medicine, Japan.

出版信息

Neuroscience. 1993 Mar;53(2):519-26. doi: 10.1016/0306-4522(93)90216-3.

DOI:10.1016/0306-4522(93)90216-3
PMID:8098516
Abstract

Whole cell patch-clamp recordings were made from substantia gelatinosa neurons in the thick slice of the adult rat spinal cord, which retained an attached dorsal root to study the pharmacological properties of spontaneous and primary afferent fibre-evoked synaptic currents. The majority of substantia gelatinosa neurons tested exhibited miniature excitatory postsynaptic currents in the presence of tetrodotoxin (0.5 microM). Stimulation of primary afferent A delta fibres evoked monosynaptic and/or polysynaptic excitatory postsynaptic currents. In Mg(2+)-containing solution, 6-cyano-7-nitroquinoxaline-2,3-dione (10 microM) abolished the evoked excitatory postsynaptic currents and the miniature excitatory postsynaptic currents. 2-Amino-5-phosphonovaleric acid (50-100 microM) had little effect on the miniature excitatory postsynaptic current. In Mg(2+)-free solution, however, 6-cyano-7-nitroquinoxaline-2,3-dione reduced but did not abolish the miniature excitatory postsynaptic currents, leaving the miniature excitatory postsynaptic currents with a small amplitude and a slow time course, which were abolished by 2-amino-5-phosphonovaleric acid. At holding potentials more positive than -60 mV, stimulation of A delta fibres evoked outward postsynaptic currents in 11 out of 28 substantia gelatinosa neurons. The evoked inhibitory postsynaptic currents were abolished in seven out of 11 neurons by either strychnine (0.5 microM) or bicuculline (10 microM), and in the remaining four neurons by the combination of both antagonists.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在成年大鼠脊髓厚切片的胶状质神经元上进行全细胞膜片钳记录,该切片保留附着的背根以研究自发的和初级传入纤维诱发的突触电流的药理学特性。在存在河豚毒素(0.5微摩尔)的情况下,大多数被测试的胶状质神经元表现出微小兴奋性突触后电流。刺激初级传入Aδ纤维诱发单突触和/或多突触兴奋性突触后电流。在含镁溶液中,6-氰基-7-硝基喹喔啉-2,3-二酮(10微摩尔)消除了诱发的兴奋性突触后电流和微小兴奋性突触后电流。2-氨基-5-磷酸戊酸(50 - 100微摩尔)对微小兴奋性突触后电流影响很小。然而,在无镁溶液中,6-氰基-7-硝基喹喔啉-2,3-二酮减少但并未消除微小兴奋性突触后电流,使微小兴奋性突触后电流幅度变小且时程变慢,而这被2-氨基-5-磷酸戊酸所消除。在钳制电位比 - 60毫伏更正时,刺激Aδ纤维在28个胶状质神经元中的11个中诱发外向突触后电流。在11个神经元中的7个中,诱发的抑制性突触后电流被士的宁(0.5微摩尔)或荷包牡丹碱(10微摩尔)消除,在其余4个神经元中被两种拮抗剂联合消除。(摘要截短于250字)

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