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Development of a pharmacological target profile for muscarinic agonists
Author(s) -
Widzowski Daniel V.,
Bialobok Paul,
Kucera Kris E.,
Mihut Roberta,
Sitar Shawn,
Knowles Marilyn,
Stagnitto Mary,
Howell Andrew,
McCreedy Sally,
Machulskis Anthony,
Zongrone John,
Gordon Jack,
Marler Matthew,
Wu Edwin S.C.,
Mullen George,
Triggle David J.,
Blosser James
Publication year - 1997
Publication title -
drug development research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.582
H-Index - 60
eISSN - 1098-2299
pISSN - 0272-4391
DOI - 10.1002/(sici)1098-2299(199702)40:2<117::aid-ddr3>3.0.co;2-o
Subject(s) - muscarinic acetylcholine receptor , agonist , muscarinic acetylcholine receptor m1 , muscarinic agonist , pharmacology , cholinergic , carbachol , chemistry , cholinesterase , muscarinic acetylcholine receptor m2 , intrinsic activity , in vivo , medicine , partial agonist , endocrinology , receptor , biology , microbiology and biotechnology
The purpose of these studies was to determine the levels of intrinsic activity in vitro at muscarinic receptor pharmacological subtypes (M 1 , M 2 , and M 3 ) that would optimize cognitive activity while minimizing acute adverse cholinergic effects in vivo. These levels of intrinsic efficacy at M 1 , M 2 , and M 3 receptor subtypes, the target profile, could then be used to assess novel compounds for antidementia potential. To accomplish this, a series of muscarinic agonists (spirofuranone analogues) was prepared, and compounds with variable intrinsic activity at M 1 , M 2 , and M 3 receptor subtypes were selected for characterization in a series of in vivo tests (reversal of scopolamine‐induced memory impairment, and agonist‐induced salivation, lacrimation, diarrhea, hypothermia, and bradycardia). Memory enhancement was found to correspond best to M 1 activity with an apparent threshold of intrinsic activity of approximately 50% in human M 1 ‐transfected CHO cells. Surprisingly, a preferential M 3 agonist (ARL 16037) produced a partial reversal of scopolamine‐induced memory impairment, but only at high doses that resulted in severe diarrhea. However, it was unclear whether this memory effect was due to the weak M 1 or strong M 3 agonist activity of this compound. Three muscarinic agonists (ARL 14995, ARL 15467, and ARL 15424) reversed the scopolamine‐induced memory deficits, as well as the cholinesterase inhibitor tacrine, suggesting that muscarinic agonists may be at least as clinically effective as cholinesterase inhibitors. Acute cholinergic side effects (diarrhea, salivation, lacrimation) corresponded best to M 3 activity (contraction of guinea pig trachea) and were greatly diminished with in vitro intrinsic M 3 activity of 50% or less. Agonist‐induced heart rate reduction corresponded best to M 2 receptor efficacy (inhibition of rat heart adenylyl cyclase). Identification of compounds without detectable in vitro intrinsic activity but with measurable heart rate effects suggested that signal amplification at M 2 receptors in vitro limited detection of weak partial agonists. Development of the target profile has proven useful in rapid evaluation of compounds for optimization of muscarinic pharmacological properties. Drug Dev. Res. 40:117–132, 1997. © 1997 Wiley‐Liss, Inc.