Literature DB >> 15211691

Mechanisms determining cholinergic neural responses in airways of young and mature rabbits.

Gary L Larsen1, Joan Loader, Dee Dee Nguyen, Cori Fratelli, Azzeddine Dakhama, Giuseppe N Colasurdo.   

Abstract

Neural pathways help control airway caliber and responsiveness. Yet little is known of how neural control changes as a function of development. In rabbits, we found electrical field stimulation (EFS) of airway nerves led to more marked contractile responses in 2- vs. 13-week-old animals. This enhanced response to EFS may be due to prejunctional, junctional, and/or postjunctional neural mechanisms. We assessed these mechanisms in airways of 2- and 13-week-old rabbits. The contractile responses to methacholine did not differ in the groups, suggesting postjunctional neural events are not primarily responsible for differing responses to EFS. To address junctional events, acetylcholinesterase (AChE) was measured (spectrophotometry). AChE was elevated in 2-week-olds. However, this should lead to less and not greater responses. Prejunctionally, EFS-induced acetylcholine (ACh) release was assessed by HPLC. Airways of 2-week-old rabbits released significantly more ACh than airways from mature rabbits. Choline acetyltransferase, a marker of cholinergic nerves, was not different between groups, suggesting that more ACh release in young rabbits was not due to increased nerve density. ACh release in the presence of polyarginine increased significantly in both groups, supporting the presence of functional muscarinic autoreceptors (M2) at both ages. Because substance P (SP) increases release of ACh, SP was measured by ELISA. This neuropeptide was significantly elevated in airways of younger rabbits. Nerve growth factor (NGF) increased SP and was also significantly increased in airways from younger rabbits. This work suggests that increases in EFS-induced responsiveness in young rabbits are likely due to prejunctional events with enhanced release of ACh. Increases in NGF and SP early in life may contribute to this increased responsiveness. Copyright 2004 Wiley-Liss, Inc.

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Year:  2004        PMID: 15211691     DOI: 10.1002/ppul.20060

Source DB:  PubMed          Journal:  Pediatr Pulmonol        ISSN: 1099-0496


  5 in total

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Authors:  Dawn D Hunter; Lynnsey A Carrell-Jacks; Tom P Batchelor; Richard D Dey
Journal:  Am J Respir Cell Mol Biol       Date:  2010-11-12       Impact factor: 6.914

2.  Three days after a single exposure to ozone, the mechanism of airway hyperreactivity is dependent on substance P and nerve growth factor.

Authors:  Kirsten C Verhein; Mehdi S Hazari; Bart C Moulton; Isabella W Jacoby; David B Jacoby; Allison D Fryer
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2010-11-05       Impact factor: 5.464

3.  Estrogen determines sex differences in airway responsiveness after allergen exposure.

Authors:  Shigeki Matsubara; Christina H Swasey; Joan E Loader; Azzeddine Dakhama; Anthony Joetham; Hiroshi Ohnishi; Annette Balhorn; Nobuaki Miyahara; Katsuyuki Takeda; Erwin W Gelfand
Journal:  Am J Respir Cell Mol Biol       Date:  2007-12-06       Impact factor: 6.914

4.  Interleukin (IL)-1 regulates ozone-enhanced tracheal smooth muscle responsiveness by increasing substance P (SP) production in intrinsic airway neurons of ferret.

Authors:  Z-X Wu; J S Barker; T P Batchelor; R D Dey
Journal:  Respir Physiol Neurobiol       Date:  2008-07-31       Impact factor: 1.931

5.  Prenatal and early, but not late, postnatal exposure of mice to sidestream tobacco smoke increases airway hyperresponsiveness later in life.

Authors:  Zhong-Xin Wu; Dawn D Hunter; Vincent L Kish; Katherine M Benders; Thomas P Batchelor; Richard D Dey
Journal:  Environ Health Perspect       Date:  2009-05-22       Impact factor: 9.031

  5 in total

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