Mechanism of Action of Hypoxia in Tracheal Smooth Muscle (TSM) with a Note on the Role of the Series Elastic Component

Author(s):  
N. L. Stephens
1996 ◽  
Vol 271 (5) ◽  
pp. C1716-C1724 ◽  
Author(s):  
D. Salvail ◽  
A. Alioua ◽  
E. Rousseau

The biophysical and pharmacological characteristics of unitary Cl- currents from bovine tracheal smooth muscle cells were studied after reconstitution of microsomal vesicles into planar lipid bilayers. Two types of currents were recorded simultaneously in KCl buffer: the well-defined Ca(2+)-dependent K+ conductance [GK(Ca)] and a much smaller Cl- current, indicating that the Cl- channels under scrutiny originate from the same membrane as the GK(Ca)-type channels, the plasma membrane of airway smooth muscle (ASM) cells. The GK(Ca) activities were eliminated by the use of CsCl buffer. The average unitary Cl- conductance measured in 50 mM trans-250 mM cis CsCl was 77 +/- 6 pS (n = 21), and the reversal potential measured in various CsCl gradients followed the Cl- equilibrium potential as determined from the Nernst equation. In contrast with the previous reports describing the Ca2+ sensitivity of macroscopic ASM Cl- currents, this channel was found to be insensitive to cytoplasmic and extracellular Ca2+ levels. Phosphorylation cocktails, including protein kinases A, G, or C, did not alter the activity of the channel nor did changes in pH. Among a series of Cl- channel inhibitors, 4,4'-diisothiocyanostilbene-2, 2'-disulfonic acid [50% effective concentration (EC50) = 30 microM] and 5-nitro-2-(3-phenylpropylamino) benzoic acid (EC50 = 130 microM) were the most potent blockers of the current examined. The exact role of this surface Cl- conductance remains unclear, and its involvement in cellular activity needs further investigation.


1998 ◽  
Vol 274 (2) ◽  
pp. L220-L225 ◽  
Author(s):  
I. McGrogan ◽  
L. J. Janssen ◽  
J. Wattie ◽  
P. M. O’Byrne ◽  
E. E. Daniel

To investigate the role of prostaglandin (PG) E2 in allergen-induced hyperresponsiveness, dogs inhaled either the allergen Ascaris suum or vehicle (Sham). Twenty-four hours after inhalation, some animals exposed to allergen demonstrated an increased responsiveness to acetylcholine challenge in vivo (Hyp-Resp), whereas others did not (Non-Resp). Strips of tracheal smooth muscle, either epithelium intact or epithelium denuded, were suspended on stimulating electrodes, and a concentration-response curve to carbachol (10−9 to 10−5 M) was generated. Tissues received electrical field stimulation, and organ bath fluid was collected to determine PGE2content. With the epithelium present, all three groups contracted similarly to 10−5 M carbachol, whereas epithelium-denuded tissues from animals that inhaled allergen contracted more than tissues from Sham dogs. In response to electrical field stimulation, Hyp-Resp tissues contracted less than Sham tissues in the presence of epithelium and more than Sham tissues in the absence of epithelium. PGE2release in the muscle bath was greater in Non-Resp tissues than in Sham or Hyp-Resp tissues when the epithelium was present. Removal of the epithelium greatly inhibited PGE2release. We conclude that tracheal smooth muscle is hyperresponsive in vitro after in vivo allergen exposure only when the modulatory effect of the epithelium, largely through PGE2 release, is removed.


1998 ◽  
Vol 274 (6) ◽  
pp. C1653-C1660 ◽  
Author(s):  
Y. S. Prakash ◽  
Mathur S. Kannan ◽  
Timothy F. Walseth ◽  
Gary C. Sieck

The purpose of the present study was to determine whether cyclic ADP-ribose (cADPR) acts as a second messenger for Ca2+ release through ryanodine receptor (RyR) channels in tracheal smooth muscle (TSM). Freshly dissociated porcine TSM cells were permeabilized with β-escin, and real-time confocal microscopy was used to examine changes in intracellular Ca2+ concentration ([Ca2+]i). cADPR (10 nM–10 μM) induced a dose-dependent increase in [Ca2+]i, which was blocked by the cADPR receptor antagonist 8-amino-cADPR (20 μM) and by the RyR blockers ruthenium red (10 μM) and ryanodine (10 μM), but not by the inositol 1,4,5-trisphosphate receptor blocker heparin (0.5 mg/ml). During steady-state [Ca2+]ioscillations induced by acetylcholine (ACh), addition of 100 nM and 1 μM cADPR increased oscillation frequency and decreased peak-to-trough amplitude. ACh-induced [Ca2+]ioscillations were blocked by 8-amino-cADPR; however, 8-amino-cADPR did not block the [Ca2+]iresponse to a subsequent exposure to caffeine. These results indicate that cADPR acts as a second messenger for Ca2+ release through RyR channels in TSM cells and may be necessary for initiating ACh-induced [Ca2+]ioscillations.


2009 ◽  
Vol 36 (7) ◽  
pp. 619-625 ◽  
Author(s):  
Catalina Romero-Méndez ◽  
Paola Algara-Suárez ◽  
Sergio Sánchez-Armass ◽  
Peter B Mandeville ◽  
Ulises Meza ◽  
...  

The internal mechanical condition of an excited muscle has been examined by applying quick stretches at various moments after a maximal shock. At the end of the latent period there is an abrupt change of state, the contractile component suddenly becoming capable of bearing a load equal to the maximum tension set up in an isometric tetanus. The intensity of the active state produced by a shock is greatest at the start, is maintained for a time and then declines as relaxation sets in. The properties of the fully active state are defined by the three constants of the characteristic equation relating speed of shortening to load. A muscle consists mechanically of three components: (1) a contractile one, (2) an undamped series elastic one and (3) a parallel elastic one. The complication provided by (3) is avoided by working with small initial loads. The load-extension relation of the series elastic component has been determined. Its extensibility is high at small loads, becoming much less at greater ones. The full isometric force produces an extension in it of about 10% of the muscle’s length. In an isometric tetanus the form of the myogram is fully determined by the characteristic force-velocity relation of the contractile component and the load-extension curve of the series elastic one, the former having to shorten and stretch the latter before an external tension can be manifested. In a twitch there is insufficient time, before relaxation sets in, for the full tension to be developed. When the tension is raised sufficiently by a quick stretch applied early after a shock the contractile component cannot shorten as it would normally and the heat of shortening is absent. The heat of activation is probably a by-product of the process by which the sudden change of state from rest to full activity occurs. When a muscle is subjected to a tension rather greater than it can bear it lengthens slowly; to a tension considerably greater it ‘gives’ or ‘slips’. When a muscle is stretched rapidly a transitory overshoot of tension occurs followed by ‘slip’. During the disappearance of this extra tension heat is produced, as in the ‘cold drawing’ of a wire or thread. An analogous process occurs in relaxation under a load. When two shocks are applied in succession, the second restores the active state to its full intensity, from which it has declined to an extent depending on the interval after the first one. If, under isometric conditions, the series elastic component is still partly stretched at the moment when the second response occurs, the total tension developed is greater. This is the origin of the so-called ‘supernormal phase’ and the basis of the greater tension maintained in atetanic contraction. During a tetanus each shock restores the active state of the muscle to its full intensity. It seems reasonably certain that excitation of a muscle fibre occurs at its surface. It has been suggested that contraction is set up inside by the arrival of some chemical substance diffusing inwards after liberation a t the surface. The onset, however, of full activity occurs so soon after a shock that diffusion is far too slow to account for it. A process, not a substance, must carry activation inwards.


1992 ◽  
Vol 146 (6) ◽  
pp. 1548-1552 ◽  
Author(s):  
Hiromasa Inoue ◽  
Hiroshi Koto ◽  
Shohei Takata ◽  
Hisamichi Aizawa ◽  
Togo Ikeda

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