Effect of external Cd2+ and other divalent cations on carbachol‐activated non‐selective cation channels in guinea‐pig ileum.
書誌事項
- 公開日
- 1991-10
- 権利情報
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- http://onlinelibrary.wiley.com/termsAndConditions#vor
- DOI
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- 10.1113/jphysiol.1991.sp018802
- 公開者
- Wiley
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説明
<jats:p>1. Inhibitory actions of the external divalent cations, Cd2+, Ni2+, Mn2+ and Co2+ on carbachol (CCh)‐induced inward current (Ins,ACh) were investigated in caesium aspartate‐loaded single longitudinal smooth muscle cells of guinea‐pig ileum, using a rapid solution‐switching device, under voltage‐clamped conditions. 2. Cd2+ (20‐1000 microM), when added to the external solution, reduced Ins,ACh rapidly and reversibly. This effect occurred dose dependently, the relationship being adequately described by a Michaelis‐Menten equation with a Hill coefficient (n) of 1.0 and a dissociation constant (Kd) of 98 microM. 3. The inhibitory action of Cd2+ was associated neither with agonist concentration (CCh) nor with changes in reversal potential, and was voltage independent. 4. The appearance and removal of the effect of Cd2+ were both rapid (a few hundred milliseconds), in sharp contrast with a relatively slow time course of atropine or CCh action (of the order of seconds). 5. Other divalent cations (Ni2+, Mn2+, Co2+, Mg2+) applied externally also suppressed Ins,ACh, but less potently. The sequence of apparent potency was Cd2+ (98 microM) greater than or equal to Ni2+ (131 microM) much greater than Co2+ (700 microM) greater than or equal to Mn2+ (1000 microM) much greater than Mg2+ (approximately 10 mM). 6. External Ca2+ increased Ins,ACh dose dependently and antagonized the inhibitory effect of Cd2+. However, this effect may not be a simple competition with Cd2+. 7. These results show that external divalent cations strongly modulate Ins,ACh channels, possibly through direct interaction with the channel protein.</jats:p>
収録刊行物
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- The Journal of Physiology
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The Journal of Physiology 442 (1), 447-463, 1991-10
Wiley
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詳細情報 詳細情報について
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- CRID
- 1361699995471665792
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- ISSN
- 14697793
- 00223751
- http://id.crossref.org/issn/00223751
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- データソース種別
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- Crossref

