Key result
Long-term exposure to carbachol substantially reduced cardiac muscarinic K+ channel activity due to desensitization, without internalization of the channel itself.
Long-term desensitization of the cardiac M2 muscarinic receptor system involves a decline in muscarinic K+ channel function without channel internalization.
Functional decline without internalization may underlie cardiac M2 desensitization; hypothesis-generating in animals, requires human validation.
The cardiac M2 muscarinic receptor/G protein/K+ channel system was studied in neonatal rat atrial cells cultured with and without 10 microM carbachol (CCh) for 24 h. Channel activity in CCh-pretreated cells was substantially reduced as a result of long-term desensitization regardless of whether the channel was activated by ACh in cell-attached patches or GTP in inside-out patches. Channel activity in CCh-pretreated cells was also low when the receptor was bypassed and the G protein and channel were directly activated by [gamma-S]GTP or both the receptor and G protein were bypassed and the channel was directly activated by trypsin. Finally, in CCh-pretreated cells, the whole cell K+ current was low when the channel was activated via the independent adenosine receptor. This suggests that the channel is involved in long-term desensitization. However, in CCh-pretreated cells, although the receptor was internalized, there was no internalization of the channel. We suggest that the function of the muscarinic K+ channel declines in long-term desensitization of the cardiac M2 muscarinic receptor/G protein/K+ channel system.
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Shui et al. (2001) studied this question. Carbachol (CCh) vs. Without carbachol was evaluated on Channel activity and whole cell K+ current. Long-term exposure to carbachol substantially reduced cardiac muscarinic K+ channel activity due to desensitization, without internalization of the channel itself.
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