Abstract
Rat M3 mAChR subtype was stably expressed in RAT 1 cells. Investigation of the pharmacological and biochemical properties of the cloned M3 receptors revealed that they mediate phosphoinositide hydrolysis but not adenylate cyclase inhibition. The similarities and differences between the properties of cloned rat M1 and M3 receptors are discussed.
| Original language | English |
|---|---|
| Pages (from-to) | 174-178 |
| Number of pages | 5 |
| Journal | FEBS Letters |
| Volume | 239 |
| Issue number | 2 |
| DOIs | |
| State | Published - 7 Nov 1988 |
Keywords
- Muscarinic receptor
- Phosphoinositide hydrolysis
- Receptor ligand binding
- Receptor subtype comparison
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