Ernst M. App
University of Alberta
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Featured researches published by Ernst M. App.
The Journal of Physiology | 2003
Rebecca S. Lam; Ernst M. App; Drew Nahirney; Artur Szkotak; Maria A. Vieira-Coelho; Malcolm King; Marek Duszyk
Previous studies have shown that α2 adrenoceptor (α2AR) agonists inhibit electrolyte secretion in colonic epithelia, but little is known about the molecular mechanisms involved in this process. In this study we examined the effect of α2AR activation on transepithelial anion secretion across isolated murine colonic epithelium. We found that α2AR agonists, UK 14,304, clonidine and medetomidine were potent inhibitors of anion secretion, especially in the proximal colon. Short circuit current measurements (Isc) in colonic epithelia from normal and cystic fibrosis (CF) mice showed that α2AR agonists inhibited basal cystic fibrosis transmembrane conductance regulator (CFTR)‐mediated Cl− secretion but had no effect on CFTR activation by cAMP‐dependent phosphorylation. Apical administration of an ionophore, nystatin (90 μg ml−1), was used to investigate the effect of UK 14,304 on basolateral K+ transport. The Na+–K+‐ATPase current, measured as ouabain‐sensitive current in the absence of ion gradients, was unaltered by pretreatment of the tissue with UK 14,304 (1 μm). In the presence of a basolaterally directed K+ gradient, UK 14,304 significantly reduced nystatin‐activated Isc indicating that activation of α2ARs inhibits basolateral K+ channels. Studies with selective K+ channel inhibitors and openers showed that α2AR agonists inhibited KATP channels that were tonically active in mouse colonic epithelia. RT‐PCR and pharmacological studies suggested that these channels could be similar to vascular smooth muscle KATP channels comprising Kir6.1/SUR2B or Kir6.2/SUR2B subunits. Inhibition of anion secretion by α2AR agonists required activation of pertussis toxin‐sensitive Gi/o proteins, but did not involve classical second messengers, such as cAMP or Ca2+. In summary, α2ARs inhibit anion secretion in colonic epithelia by acting on basolateral KATP channels, through a process that does not involve classical second messengers.
Biorheology | 1990
Ernst M. App; Malcolm King
The transepithelial potential difference (PD) value represents an integral of ion fluxes across the epithelium, and relates to the regulation of airway fluid. We studied six healthy two day old husky puppies for their tracheal mucus rheology and bioelectric properties, since this data in newborns are still unknown. PD (-mV, epithelium vs. subcutaneous space) was measured using the agar bridge technique in two locations - lower trachea and subglottic region. For the rheological analysis, the magnetic microrheometer was employed; data are presented as mechanical impedance log G* and loss tangent tan delta (1 rad/s). The mucus collection rate (mg/min) and the solid content (%) were determined by gravimetry. Mucociliary clearability, normalized to frog mucus, (MCFP) was determined directly by the frog palate method; a cough clearability index (CCI) was computed from simulated cough machine data obtained with mucus-like gels. The mucus collection rates and PD values were considerably lower than those observed in adult dogs; the mechanical impedance values were also reduced in comparison with adult data. The PD profile within the trachea (-13.9 +/- 1.2 mV lower trachea vs. -18.4 +/- 1.4 mV subglottical, i.e. more negative subglottically), however, is similar to that observed in adult dogs. Intratracheal profiles in mucus collection rate and mucus rheology were also comparable between puppies and adult dogs. The low collection rates in puppies, particularly in lower trachea, could indicate either reduced mucus volume or slower clearance. PD and collection rate correlated very strongly (r = 0.82, p = 0.0003). PD also correlated negatively with log G* (r = 0.73, p = 0.003) and positively with tan delta (r = 0.58, p = 0.03). MCFP and % solids correlated positively (r = 0.84, p = 0.0012), in contradistinction to the usual relationship, perhaps due to the presence of non-glycoprotein components that do not contribute to crosslink formation. The apparent maturation of airway bioelectric properties, mucus collection rate and mucus viscoelasticity are all consistent with the maturation of mucociliary clearance, which has previously been reported.
The American review of respiratory disease | 1990
Ernst M. App; Malcolm King; Renate Helfesrieder; Dieter Köhler; Heinrich Matthys
Chest | 1998
Ernst M. App; Rita Kieselmann; Dietrich Reinhardt; Hermann Lindemann; Bonnie Dasgupta; Malcolm King; Peter Brand
The American review of respiratory disease | 1993
R. P. Tomkiewicz; Ernst M. App; J. G. Zayas; Oscar A. Ramirez; N. Church; R. C. Boucher; M. R. Knowles; Malcolm King
Chest | 1998
Ernst M. App; Rita Kieselmann; Dietrich Reinhardt; Hermann Lindemann; Bonnie Dasgupta; Malcolm King; Peter Brand
Canadian Respiratory Journal | 2004
Ulrich Baumann; Malcolm King; Ernst M. App; Shusheng Tai; Armin König; Julia J Fischer; Torsten Zimmermann; Wolfgang Sextro; Horst von der Hardt
Pulmonary Pharmacology | 1995
R.P. Tomkiewicz; Ernst M. App; G T De Sanctis; M. Coffiner; P. Maes; B.K. Rubin; Malcolm King
Pediatric Pulmonology | 1990
Bruce K. Rubin; Sam Marcushamer; Israel Priel; Ernst M. App
Journal of Applied Physiology | 1990
G. T. De Sanctis; Ernst M. App; J. K. Trask; B. I. De Sanctis; J. E. Remmers; Francis H. Y. Green; S. F. P. Man; Malcolm King