Abstract:
:Isolated Helix neurons were internally perfused under voltage-clamp, with drugs applied by the 'concentration clamp' which allowed an extremely rapid switching of the external solution. 4-Aminopyridine (4-AP) at more than 3 X 10(-4) M induced a chloride current (ICl) which could be blocked by D-tubocurarine. Acetylcholine (ACh) also induced ICl which was similarly blocked. Simultaneous application of 4-AP and ACh resulted in potentiation of ICl over the sum of respective currents. When preceded by either one, the other ICl was reduced in size, showing cross-desensitization. These data indicate that 4-AP activates ICl by binding to the cholinergic receptors, and reduces ACh-induced ICl by desensitizing a common receptor-channel complex.
journal_name
Neurosci Lettjournal_title
Neuroscience lettersauthors
Ikemoto Y,Akaike N,Ono Kdoi
10.1016/0304-3940(87)90189-3subject
Has Abstractpub_date
1987-04-23 00:00:00pages
42-6issue
1eissn
0304-3940issn
1872-7972pii
0304-3940(87)90189-3journal_volume
76pub_type
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journal_title:Neuroscience letters
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journal_title:Neuroscience letters
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journal_title:Neuroscience letters
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pub_type: 临床试验,杂志文章,随机对照试验
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pub_type: 杂志文章
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更新日期:1985-09-06 00:00:00
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journal_title:Neuroscience letters
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journal_title:Neuroscience letters
pub_type: 杂志文章
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journal_title:Neuroscience letters
pub_type: 杂志文章
doi:10.1016/0304-3940(85)90122-3
更新日期:1985-05-14 00:00:00
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journal_title:Neuroscience letters
pub_type: 杂志文章
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更新日期:2004-11-11 00:00:00
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journal_title:Neuroscience letters
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更新日期:2000-04-14 00:00:00
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journal_title:Neuroscience letters
pub_type: 杂志文章
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更新日期:1998-05-22 00:00:00