ライフサイエンスコーパス: muscarinic receptor agonist

コーパス検索結果 (１語後でソート)

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1 served more than 30 min after removal of the muscarinic receptor agonist.

2 uction following injection of pilocarpine, a muscarinic receptor agonist.

3 s competitively inhibited the binding of the muscarinic receptor agonist, [3H]quinuclidinyl benzilate

4 independent, because it is not influenced by muscarinic receptor agonists and antagonists or by treat

5 ationship between the efficacy of seven M(3) muscarinic receptor agonists and their rate of dissociat

6 Acetyl-beta-methylcholine (MCh), a muscarinic receptor agonist, applied by either superfusi

7 Muscarinic receptor agonists are characterized by appare

8 the L(7) dorsal horn increasing doses of the muscarinic receptor agonist bethanechol, but not the nic

9 The muscarinic receptor agonist 'BuTAC' was previously shown

10 e studied for their response to carbachol, a muscarinic receptor agonist, by measuring the increase i

11 The muscarinic receptor agonist carbachol activated ERK1/2 b

12 Here we demonstrate that the muscarinic receptor agonist carbachol activates AMPKalph

13 ted by EGF with those induced by agents (the muscarinic receptor agonist carbachol and thapsigargin (

14 he Ca2+-ATPase inhibitor thapsigargin or the muscarinic receptor agonist carbachol further augmented

15 Activation of G(i) protein with the muscarinic receptor agonist carbachol protected against

16 ncreased as rapidly as that initiated by the muscarinic receptor agonist carbachol, which promoted an

17 to mediate bronchoconstriction caused by the muscarinic receptor agonist carbachol.

18 tance that was reduced on application of the muscarinic receptor agonist carbachol.

19 trol of the concentration gradient of chosen muscarinic receptor agonists (carbachol, acetylcholine,

20 cells with anti-adrenergic reagents such as muscarinic receptor agonist, carbachol (10(-5)m), or a b

21 At basal 2.8 mmol/l glucose, the muscarinic receptor agonist carbamylcholine chloride (CC

22 n, we identified a potent and selective M(1) muscarinic receptor agonist from a novel structural clas

23 rat following injection of small amounts of muscarinic receptor agonists into the caudal oral pontin

24 crease in TRPC3-GFP TIRFM in response to the muscarinic receptor agonist methacholine or the syntheti

25 Spinally administered muscarinic receptor agonists or acetylcholinesterase inh

26 Spinally administered muscarinic receptor agonists or acetylcholinesterase inh

27 ate post-training intra-BLC infusions of the muscarinic receptor agonist oxotremorine (10 ng/0.2 micr

28 ere bilaterally infused in the NAcc with the muscarinic receptor agonist oxotremorine methiodide (OXO

29 Effects of a muscarinic receptor agonist oxotremorine-M (oxo-M) on bl

30 RTN chemoreceptors to ACh was mimicked by a muscarinic receptor agonist (oxotremorine; 1 mum), and b

31 tagonist, scopolamine, augments, whereas the muscarinic receptor agonist, oxotremorine, attenuates be

32 currently limited to medications (e.g., the muscarinic receptor agonists pilocarpine and cevimeline)

33 salivation are limited to medications (e.g., muscarinic receptor agonists: pilocarpine and cevimeline

34 We found that treatment with muscarinic receptor agonist resulted in decreased APP le

35 he APP processing in vivo, we administered a muscarinic receptor agonist (RS86) to normal or aged rat

36 s, we evaluated the ability of the selective muscarinic receptor agonist (SMRA) xanomeline to stimula

37 r to behavioral testing, oxotremorine, an M2 muscarinic receptor agonist that reduces cholinergic rel

38 Carbachol, a known nAChR and muscarinic receptor agonist, up-regulated both alpha4bet

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