Affiliation:
1. Department of Pediatrics, University of Tennessee Health Science Center, Memphis, Tennessee
2. Departments of Pediatrics and Veterinary Pathobiology, University of Minnesota, Minneapolis, Minnesota
3. Division of Pulmonary, Allergy and Critical Care Medicine, Department of Medicine, Thomas Jefferson University, Philadelphia, Pennsylvania
Abstract
Abstract
Background Superoxide anions (O2
−) have multiple effects on pulmonary parenchyma altering cell proliferation, cellular metabolism, and airway smooth muscle (ASM) contraction. Intracellular calcium ([Ca2+]i) concentration plays a significant role in the regulation of ASM contraction, relaxation, proliferation, and gene expression.
Objective We investigated the effects of O2
− on agonist-stimulated changes in [Ca2+]i in ASM cells.
Design/Methods Fura-2 AM-loaded, freshly isolated porcine ASM (PASM) cells were used to examine [Ca2+]i release in response to acetylcholine (ACh), histamine, endothelin, caffeine, and thapsigargin (TPG) in the presence or absence of extracellular Ca2+.
Results Exposure of PASM cells to xanthine and xanthine oxidase (X + XO) resulted in a time-dependent generation of O2
−, inhibited by superoxide dismutase (SOD). Preincubating PASM cells with X + XO for 15- or 45-minute inhibited net [Ca2+]i responses to ACh, histamine, caffeine, and TPG compared with control cells. Pretreating PASM cells with SOD for 30 minutes mitigated the inhibitory effect of X + XO treatment on ACh-induced Ca2+ elevation suggesting role of O2
−. X + XO treatment also inhibited caffeine- and TPG-induced Ca2+ elevation suggesting effect of O2
− on [Ca2+]i release and reuptake mechanisms.
Conclusion Superoxide attenuates [Ca2+]i release, reuptake, and may interfere with physiological functions of ASM cells.
Funder
Academic Health Center, University of Minnesota
National Institutes of Health to Mathur Kannan