A sustained inward current activated at the diastolic potential range in rabbit sino‐atrial node cells.
A sustained inward current activated at the diastolic potential range in rabbit sino‐atrial node cells.
复制标题
兔窦房结细胞在舒张电位范围内激活持续的内向电流。
DOI:
10.1113/jphysiol.1995.sp020563
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发表时间:
1995
期刊:
影响因子:
--
通讯作者:
A. Noma
中科院分区:
文献类型:
--
作者:
Jiqing Guo;K. Ono;A. Noma
1. After blocking both the hyperpolarization‐activated current and the membrane K+ conductance, depolarizations from ‐80 mV to between ‐70 and ‐50 mV induced a sustained current in sino‐atrial node cells. We have tentatively designated this current Ist. 2. Ist was blocked by both organic and inorganic Ca2+ channel blockers, but was insensitive to tetrodotoxin (30 microM). Isoprenaline increased Ist. 3. The peak of Ist (at about ‐50 mV) was increased to 149 +/‐ 13% (n = 8, P < 0.01) by lowering the external Ca2+ concentration ([Ca2+]o) from 1.8 to 0.1 mM, in contrast to the marked depression of the L‐type Ca2+ current. In 0.1 mM [Ca2+]o solution, the nicardipine‐sensitive current‐voltage relation showed the peak amplitude at about ‐50 mV and a reversal potential of +37.4 +/‐ 4.4 mV (n = 5). The isoprenaline‐sensitive component also showed a reversal potential of about +30 mV. 4. Reducing [Na+]o from 140 to 70 mM in 0.1 mM [Ca2+]o decreased Ist to 53 +/‐ 5% (n = 7, P < 0.01). Increasing [Ca2+]o or [Mg2+]o decreased the amplitude of Ist. The half‐maximum concentration of Mg2+ inhibition was 2.2 mM. 5. At 1.8 mM [Ca2+]o, Ist was inactivated by clamping for 5s at ‐10 mV, and gradually recovered after repolarization to ‐80 mV with a half‐time of 1.36 +/‐ 0.4 s (n = 6). 6. The transitional sino‐atrial node cell had minimal amplitude of Ist. 7. These characteristics of Ist are qualitatively comparable to those of the monovalent cation conductance of the L‐type Ca2+ channel induced by depleting external divalent cations to the micromolar range. We conclude that Ist is generated by a novel subtype of L‐type Ca2+ channel.
DOI:
10.1073/pnas.86.5.1689
发表时间:
1989-03-01
影响因子:
11.1
作者:
LLINAS, R;SUGIMORI, M;CHERKSEY, B
通讯作者:
CHERKSEY, B
影响因子:
20.1
作者:
HIRANO, Y;MOSCUCCI, A;JANUARY, CT
通讯作者:
JANUARY, CT