M. Yamakage et al., Different inhibitory effects of volatile anesthetics on T- and L-type voltage-dependent Ca2+ channels in porcine tracheal and bronchial smooth muscles, ANESTHESIOL, 94(4), 2001, pp. 683-693
Citations number
47
Categorie Soggetti
Aneshtesia & Intensive Care","Medical Research Diagnosis & Treatment
Background: The distal airway is more important in the regulation of airflo
w resistance than is the proximal airway, and volatile anesthetics have a g
reater inhibitory effect on distal airway muscle tone. The authors investig
ated the different reactivities of airway smooth muscles to volatile anesth
etics by measuring porcine tracheal or bronchial (third to fifth generation
) smooth muscle tension and intracellular concentration of free Ca2+ ([Ca2](i)) and by measuring inward Ca2+ currents (I-Ca) through voltage-dependen
t Ca2+ channels (VDCs).
Methods: Intracellular concentration of free Ca2+ was monitored by the 500-
nm light emission ratio of Ca2+ indicator fura-2, Isometric tension was mea
sured simultaneously. Whole-cell patch clamp recording techniques were used
to investigate the effects of volatile anesthetics on I-Ca in dispersed sm
ooth muscle cells. Isoflurane (0-1.5 minimum alveolar concentration) or sev
oflurane (0-1.5 minimum alveolar concentration) was introduced into a bath
solution.
Results: The volatile anesthetics tested had greater inhibitory effects on
carbachol-induced bronchial smooth muscle contraction than on tracheal smoo
th muscle contraction. These inhibitory effects by the anesthetics on muscl
e tension were parallel to the inhibitory effects on [Ca2+](i). Although tr
acheal smooth muscle cells had only L-type VDCs, some bronchial smooth musc
le cells (similar to 30%) included T-type VDC, Each of the two anesthetics
significantly inhibited the activities of both types of VDCs in a dose-depe
ndent manner; however, the anesthetics had greater inhibitory effects on T-
type VDC activity in bronchial smooth muscle.
Conclusions: The existence of the T-type VDC in bronchial smooth muscle and
the high sensitivity of this channel to volatile anesthetics seem to be, a
t least in part, responsible for the different reactivities to the anesthet
ics in tracheal and bronchial smooth muscles.