EXPRESSION OF 5-HT3 RECEPTORS IN PC12 CELLS TREATED WITH NGF AND 8-BR-CAMP

被引:35
作者
FURUKAWA, K [1 ]
AKAIKE, N [1 ]
ONODERA, H [1 ]
KOGURE, K [1 ]
机构
[1] TOHOKU UNIV, SCH MED, DEPT NEUROL, SENDAI, MIYAGI 980, JAPAN
关键词
D O I
10.1152/jn.1992.67.4.812
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
1. To determine the functional development of neurons, we applied nerve growth factor (NGF) or 8-bromo-cyclic-adenosine monophosphate (8-Br-cAMP) to PC12 cells and recorded the 5-hydroxytryptamine (5-HT)-induced response by the use of a patch-clamp technique. 2. Cultured PC12 cells expressed 5-HT-sensitive receptors, which are almost absent in untreated cells, in the continuous presence of NGF or 8-Br-cAMP for a period of 10 days. 3. Activation of the receptors by 5-HT produced a transient inward current. In a K+-free solution, the reversal potential (E5-HT) of I5-HT was + 10.3 mV, and the current-voltage (I-V) relation showed inward rectification at positive potentials. 4. The permeability ratio for monovalent cations was Na+:Li+:K+:Rb+:Cs+ = 1:1.19:0.89:0.94:0.91, indicating that a 5-HT-induced current is passing through the ligand-gated large cation channel. 5. 2-Methyl-5-HT, a specific 5-HT3 agonist, induced a similar inward current, even though the current amplitude was smaller and the activation and inactivation kinetics were slower than those of 5-HT. 6. ICS-205-930, a specific 5-HT3 antagonist, inhibited the 5-HT-induced current in a concentration-dependent manner with a noncompetitive inhibition profile. Spiperone, a 5-HT1 and 5-HT2 families antagonist, and ketanserine, 5-HT2 family antagonist, did not affect the 5-HT-induced response. 7. The time to peak (t(p)) as well as fast and slow time constants (tau(if) and tau(is)) decreased with increasing 5-HT concentration. 8. It was concluded that PC12 cells in the presence of either NGF or 8-Br-cAMP expressed 5-HT3 receptors, although the latter effect was weaker. This suggests that intracellular adenosine 3',5'-cyclic monophosphate (cAMP) plays an important role in the expression of 5-HT3 receptors in PC12 cells.
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页码:812 / 819
页数:8
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