4.7 Article

Evidence for tetrodotoxin-resistant spontaneous myogenic contractions of mouse isolated stomach that are dependent on acetylcholine

期刊

BRITISH JOURNAL OF PHARMACOLOGY
卷 179, 期 6, 页码 1187-1200

出版社

WILEY
DOI: 10.1111/bph.15685

关键词

ACh; ANO1; CaCC; interstitial cells of Cajal; myogenic contractions; nausea; stomach

资金

  1. Takeda Pharmaceuticals North America
  2. Bowel Research UK

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The mouse isolated stomach exhibited myogenic contractions that were resistant to neural activity blockade by TTX. Compounds blocking interstitial cells of Cajal activity or atropine could prevent or reduce these contractions in the presence of TTX, while neostigmine enhanced the contractions (which were antagonized by atropine), suggesting the involvement of non-neuronal acetylcholine in their regulation.
Background and Purpose Gastric pacemaker cells, interstitial cells of Cajal (ICC), are believed to initiate myogenic (non-neuronal) contractions. These become damaged in gastroparesis, associated with dysrhythmic electrical activity and nausea. We utilised mouse isolated stomach to model myogenic contractions and investigate their origin and actions of interstitial cells of Cajal modulators. Experimental Approach Intraluminal pressure was recorded following distension with a physiological volume; tone, contraction amplitude and frequency were quantified. Compounds were bath applied. Key Results The stomach exhibited regular large amplitude contractions (median amplitude 9.0 [4.7-14.8] cmH(2)O, frequency 2.9 [2.5-3.4] c.p.m; n = 20), appearing to progress aborally. Tetrodotoxin (TTX, 10(-)(6) M) had no effect on tone, frequency or amplitude but blocked responses to nerve stimulation. omega-conotoxin GVIA (10(-)(7) M) +/- TTX was without effect on baseline motility. In the presence of TTX, (1) atropine (10(-)(10)-10(-)(6) M) reduced contraction amplitude and frequency in a concentration-related manner (pIC(50) 7.5 +/- 0.3 M for amplitude), (2) CaCC channel (previously ANO1) inhibitors MONNA and CaCCinh-A01 reduced contraction amplitude (significant at 10(-)(5), 10(-)(4) M respectively) and frequency (significant at 10(-)(5) M), and (3), neostigmine (10(-)(5) M) evoked a large, variable, increase in contraction amplitude, reduced by atropine (10(-)(8)-10(-)(6) M) but unaffected (exploratory study) by the H1 receptor antagonist mepyramine (10(-)(6) M). Conclusions and Implications The distended mouse stomach exhibited myogenic contractions, resistant to blockade of neural activity by TTX. In the presence of TTX, these contractions were prevented or reduced by compounds blocking interstitial cells of Cajal activity or by atropine and enhanced by neostigmine (antagonised by atropine), suggesting involvement of non-neuronal ACh in their regulation.

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