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1 gonist), or methoctramine (a selective M2/M4 muscarinic receptor antagonist).
2 either saline or scopolamine, a nonselective muscarinic receptor antagonist.
3 ed in the presence or absence of a selective muscarinic receptor antagonist.
4 letely blocked by scopolamine (10 microM), a muscarinic receptor antagonist.
5 rendered ineffective by either nicotinic or muscarinic receptor antagonists.
6 nd can be reliably and completely blocked by muscarinic receptor antagonists.
7 r subtypes prompted development of selective muscarinic receptor antagonists.
8 drome produced by systemic administration of muscarinic receptor antagonists.
9 and characterized as potential m1 selective muscarinic receptor antagonists.
13 ntribute to a rationale for a combination of muscarinic receptor antagonists and beta-adrenoceptor ag
14 on one or both of the aromatic rings of the muscarinic receptor antagonist aprophen [(N,N-diethylami
16 endent manner by local administration of the muscarinic receptor antagonist atropine (30 and 60 micro
17 and with the iontophoretically administered muscarinic receptor antagonist atropine (400 microA cm-2
18 by intrathecal injection of the cholinergic muscarinic receptor antagonist atropine, but was not aff
21 e neuropathic rats, the inhibitory effect of muscarinic receptor antagonists (atropine and scopolamin
26 (NMDA receptor antagonist), and scopolamine (muscarinic receptor antagonist) blocked rapid plastic ch
27 harmacological treatment involves the use of muscarinic receptor antagonists, but their therapeutic e
28 nt pharmacological treatment involves use of muscarinic receptor antagonists, but their therapeutic e
29 r hand, the microinjection of scopolamine (a muscarinic receptor antagonist) did not block the induct
30 a blood-brain barrier-impermeant cholinergic muscarinic receptor antagonist, evoked results similar t
31 NMDA, metabotropic glutamate, GABA(B), and muscarinic receptor antagonists, in contrast, are mainly
32 treatment with solifenacin, an FDA-approved muscarinic receptor antagonist, increased oligodendrocyt
33 haled bronchodilators, including long-acting muscarinic receptor antagonists (LAMA) and long-acting b
35 by angiotensin type 1 (AT1) or acetylcholine muscarinic receptor antagonists (losartan and atropine).
36 e, ACh-induced rebound was blocked by the M2 muscarinic receptor antagonist methoctramine but not by
38 0, 0.03, or 0.1 mg/kg, intraperitoneally), a muscarinic receptor antagonist, or mecamylamine (0, 0.75
40 ated, 384-well format, by characterizing the muscarinic receptor antagonists pirenzepine and atropine
42 Blockade of cholinergic neurotransmission by muscarinic receptor antagonists produces profound defici
43 es report that scopolamine, an acetylcholine muscarinic receptor antagonist, produces rapid antidepre
47 clarative memory by infusing the cholinergic muscarinic receptor antagonist scopolamine into the rat
48 ction would improve depressive symptoms, the muscarinic receptor antagonist scopolamine manifested an
49 ing iontophoretic application of the general muscarinic receptor antagonist scopolamine with single-c
51 35SO4 as a label for secreted mucus, and the muscarinic receptor antagonists telenzepine for the M1 r
54 studies have suggested that the long-acting muscarinic receptor antagonist tiotropium, a drug widely
56 herapy with tiotropium bromide, an M1 and M3 muscarinic receptor antagonist, will decrease the airway
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