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成年大鼠海马体中长时程抑制诱导对快速Ca2+内流和代谢型谷氨酸受体突触激活的需求。

Requirement of rapid Ca2+ entry and synaptic activation of metabotropic glutamate receptors for the induction of long-term depression in adult rat hippocampus.

作者信息

Otani S, Connor J A

机构信息

Laboratoire de Neurobiologie et Neuropharmacologie du Developpement, Institut des Neurosciences, Universite de Paris VI, 7 Quai Saint Bernard, Paris 75005, France.

出版信息

J Physiol. 1998 Sep 15;511 ( Pt 3)(Pt 3):761-70. doi: 10.1111/j.1469-7793.1998.761bg.x.

Abstract
  1. During block of gamma-aminobutyric acid-A-mediated inhibition, low-frequency stimulation (2 Hz, 900 pulses) to Schaffer collateral-CA1 neuron synapses of adult rat hippocampus induced an N-methyl-D-aspartate receptor-independent, postsynaptic Ca2+-dependent depression of synaptic strength (long-term depression; LTD). 2. Ratio imaging with fura-2 revealed moderate dendritic [Ca2+] increases (approximately 500 nM) during only the initial approximately 30 s of the 7.5 min stimulation period. Conditioning for 30 s was, however, insufficient to induce LTD. 3. The [Ca2+] changes were insensitive to the metabotropic glutamate receptor (mGluR) antagonist (+)-alpha-methyl-4-carboxyphenylglycine (MCPG). MCPG, however, completely blocked LTD when present during conditioning. 4. The [Ca2+] changes were abolished by postsynaptic hyperpolarization (-110 mV at the soma). Hyperpolarizing neurons to -110 mV during conditioning significantly attenuated LTD induction. 5. LTD induction was also blocked by the postsynaptic presence of the protein kinase C inhibitor peptide PKC(19-36). 6. These results suggest that LTD induction in adult hippocampus by prolonged low-frequency stimulation depends on both a rapid Ca2+ influx through voltage-sensitive channels and synaptic stimulation of mGluRs which may be coupled to phospholipase C.
摘要
  1. 在γ-氨基丁酸A介导的抑制被阻断期间,对成年大鼠海马体的沙弗氏侧支-CA1神经元突触进行低频刺激(2赫兹,900个脉冲),可诱导出一种不依赖N-甲基-D-天冬氨酸受体、突触后钙依赖性的突触强度抑制(长时程抑制;LTD)。2. 用fura-2进行比率成像显示,在7.5分钟刺激期的最初约30秒内,树突状[Ca2+]适度增加(约500纳摩尔)。然而,30秒的条件刺激不足以诱导LTD。3. [Ca2+]变化对代谢型谷氨酸受体(mGluR)拮抗剂(+)-α-甲基-4-羧基苯甘氨酸(MCPG)不敏感。然而,在条件刺激期间存在MCPG时,它会完全阻断LTD。4. 突触后超极化(胞体处为-110毫伏)可消除[Ca2+]变化。在条件刺激期间将神经元超极化至-110毫伏可显著减弱LTD诱导。5. 蛋白激酶C抑制剂肽PKC(19-36)存在于突触后时,也会阻断LTD诱导。6. 这些结果表明,成年海马体中通过延长低频刺激诱导LTD既依赖于通过电压敏感通道的快速钙内流,也依赖于mGluRs的突触刺激,mGluRs可能与磷脂酶C偶联。

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