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Physiological mechanisms mediating enhanced force generation during development and immune sensitization.

Publication ,  Journal Article
Mitchell, RW; Murphy, TM; Leff, AR
Published in: Can J Physiol Pharmacol
April 1992

We examined the development of acetylcholinesterase (AChase) activity and tracheal smooth muscle (TSM) contraction elicited by acetylcholine (ACh) in a swine model of maturation and a dog model of allergic bronchospasm. Strips of TSM were tethered isometrically at optimal length and responses were expressed as a percentage of the maximum to KCl-substituted perfusate (% KCl). Maximal contraction (ATmax) to ACh in 2-week-old swine (168 +/- 8% KCl) was greater than in 10-week-old swine (142 +/- 2% KCl; p less than 0.02). The AChase inhibitor, physostigmine, augmented ACh-elicited ATmax in 10-week-old (27% increase; p less than 0.01) but not in 2-week-old swine (2% increase; p is NS) and caused a greater increase in sensitivity to muscarinic activation in 2 versus 10 week-old swine (p less than 0.02), thus demonstrating increased contraction of TSM in 2 versus 10-week-old swine, which results at least in part from reduced AChase activity in immature animals. In another study, TSM from ragweed-sensitized dogs demonstrated augmented efficacy to ACh-elicited contraction (180 +/- 6% KCl) compared with TSM from sham-sensitized, littermate controls (163 +/- 4% KCl; p less than 0.05). In the presence of physostigmine, ATmax was not different between ragweed-sensitized and control TSM.(ABSTRACT TRUNCATED AT 250 WORDS)

Duke Scholars

Published In

Can J Physiol Pharmacol

DOI

ISSN

0008-4212

Publication Date

April 1992

Volume

70

Issue

4

Start / End Page

615 / 623

Location

Canada

Related Subject Headings

  • Trachea
  • Swine
  • Potassium Chloride
  • Physostigmine
  • Physiology
  • Parasympathomimetics
  • Muscle, Smooth
  • Muscle Contraction
  • Kinetics
  • In Vitro Techniques
 

Citation

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MLA
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Mitchell, R. W., Murphy, T. M., & Leff, A. R. (1992). Physiological mechanisms mediating enhanced force generation during development and immune sensitization. Can J Physiol Pharmacol, 70(4), 615–623. https://doi.org/10.1139/y92-079
Mitchell, R. W., T. M. Murphy, and A. R. Leff. “Physiological mechanisms mediating enhanced force generation during development and immune sensitization.Can J Physiol Pharmacol 70, no. 4 (April 1992): 615–23. https://doi.org/10.1139/y92-079.
Mitchell RW, Murphy TM, Leff AR. Physiological mechanisms mediating enhanced force generation during development and immune sensitization. Can J Physiol Pharmacol. 1992 Apr;70(4):615–23.
Mitchell, R. W., et al. “Physiological mechanisms mediating enhanced force generation during development and immune sensitization.Can J Physiol Pharmacol, vol. 70, no. 4, Apr. 1992, pp. 615–23. Pubmed, doi:10.1139/y92-079.
Mitchell RW, Murphy TM, Leff AR. Physiological mechanisms mediating enhanced force generation during development and immune sensitization. Can J Physiol Pharmacol. 1992 Apr;70(4):615–623.

Published In

Can J Physiol Pharmacol

DOI

ISSN

0008-4212

Publication Date

April 1992

Volume

70

Issue

4

Start / End Page

615 / 623

Location

Canada

Related Subject Headings

  • Trachea
  • Swine
  • Potassium Chloride
  • Physostigmine
  • Physiology
  • Parasympathomimetics
  • Muscle, Smooth
  • Muscle Contraction
  • Kinetics
  • In Vitro Techniques