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代谢型谷氨酸受体刺激诱导的大鼠腹内侧下丘脑神经元内向电流的特性研究

Characterization of the inward current induced by metabotropic glutamate receptor stimulation in rat ventromedial hypothalamic neurones.

作者信息

Lee K, Boden P R

机构信息

Parke-Davis Neuroscience Research Centre, Cambridge, UK.

出版信息

J Physiol. 1997 Nov 1;504 ( Pt 3)(Pt 3):649-63. doi: 10.1111/j.1469-7793.1997.649bd.x.

Abstract
  1. Whole-cell patch clamp recordings were made from rat ventromedial hypothalamic neurones in slices of brain tissue in vitro. Bath application of 50 microM (1S,3R)-1-aminocyclopentane-1,3-dicarboxylic acid (1S,3R-ACPD) depolarized all neurones tested by activation of an inward current of approximately 55 pA at -60 mV. 2. The inward current elicited by 1S,3R-ACPD was unaffected by K+ channel blockade with external Cs+, Ba2+ or TEA. However, the current was significantly reduced by replacement of the external NaCl with either Tris-HCl or LiCl. 3. The 1S,3R-ACPD-induced current was reduced by the heavy metal ions Ni2+ or La3+ and also by the Na(+)-Ca2+ exchange current inhibitor 3',4'-dichlorobenzamil. 4. The effects of 1S,3R-ACPD were mimicked by the group I metabotropic agonist 3,5-dihydroxyphenylglycine (DHPG) but not by the group III selective agonist, L-2-amino-4-phosphonobutanoate (L-AP4). Furthermore, the effects of 1S,3R-ACPD were inhibited by the metabotropic antagonists alpha-methyl-4-carboxyphenylglycine (MCPG) and 1-aminoindan-1,5-dicarboxylic acid (AIDA) but not by the presynaptic metabotropic receptor antagonists alpha-methyl-4-phosphonophenylglycine (MPPG) or alpha-methyl-4-tetrazolylphenylglycine (MTPG). 5. Photorelease of caged GDP beta S inside neurones irreversibly blocked the 1S,3R-ACPD-induced current whilst photolysis of caged GTP gamma S inside neurones irreversibly potentiated this current. 6. The PLC inhibitor U-73,122 significantly reduced the size of the inward current induced by 1S,3R-ACPD. This effect was not mimicked by the inactive analogue U-73,343. 7. Flash photolysis of the caged calcium chelator diazo-2 inside neurones diminished the response to 1S,3R-ACPD. 8. It is concluded that group I metabotropic glutamate receptors depolarize neurones in the VMH by activation of a Na(+)-Ca2+ exchange current through a G-protein coupled increase in intracellular Ca2+.
摘要
  1. 采用全细胞膜片钳记录技术,对体外脑组织切片中的大鼠腹内侧下丘脑神经元进行记录。浴槽中加入50微摩尔(1S,3R)-1-氨基环戊烷-1,3-二羧酸(1S,3R-ACPD),在-60毫伏时,通过激活约55皮安的内向电流,使所有测试神经元发生去极化。

  2. 1S,3R-ACPD引发的内向电流不受细胞外Cs⁺、Ba²⁺或TEA对钾通道的阻断影响。然而,用Tris-HCl或LiCl替代细胞外NaCl后,电流显著降低。

  3. 1S,3R-ACPD诱导的电流被重金属离子Ni²⁺或La³⁺以及Na⁺-Ca²⁺交换电流抑制剂3',4'-二氯苯甲酰胍降低。

  4. I组代谢型谷氨酸受体激动剂3,5-二羟基苯甘氨酸(DHPG)可模拟1S,3R-ACPD的作用,但III组选择性激动剂L-2-氨基-4-膦酰丁酸(L-AP4)则不能。此外,1S,3R-ACPD的作用被代谢型拮抗剂α-甲基-4-羧基苯甘氨酸(MCPG)和1-氨基茚满-1,5-二羧酸(AIDA)抑制,但不被突触前代谢型受体拮抗剂α-甲基-4-膦酰苯甘氨酸(MPPG)或α-甲基-4-四唑基苯甘氨酸(MTPG)抑制。

  5. 神经元内笼锁GDP-β-S的光释放不可逆地阻断了1S,3R-ACPD诱导的电流,而神经元内笼锁GTP-γ-S的光解则不可逆地增强了该电流。

  6. PLC抑制剂U-73,122显著降低了1S,3R-ACPD诱导的内向电流大小。无活性类似物U-73,343未模拟出这种效应。

  7. 神经元内笼锁钙螯合剂重氮-2的闪光光解减弱了对1S,3R-ACPD的反应。

  8. 得出结论:I组代谢型谷氨酸受体通过G蛋白偶联增加细胞内Ca²⁺,激活Na⁺-Ca²⁺交换电流,使VMH中的神经元去极化。

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