Modulatory effect of laser irradiation on mastoparan-7-induced contraction

Elżbieta Grześk1, Magdalena Mackiewicz-Milewska2, Hanna Mackiewicz-Nartowicz3

  • 1Department of Pediatrics, Hematology and Oncology, Faculty of Medicine, Collegium Medicum, Nicolaus Copernicus University, 85-094 Bydgoszcz, Poland.

Biomedical Reports
|December 17, 2019
PubMed

Insights

Laser stimulation effectively inhibits mastoparan-7-induced vascular smooth muscle contraction by modulating calcium ion influx. This study demonstrates a dose-dependent effect of laser irradiation on G-protein-activated contractions.

Area of Science:

  • Physiology
  • Biophysics
  • Pharmacology

Background:

  • Mastoparan-7 activates guanine nucleotide-binding proteins (G-proteins), leading to smooth muscle contraction, apoptosis, and increased cytoplasmic calcium.
  • Vascular smooth muscle contraction is a critical physiological process regulated by G-protein signaling pathways.

Purpose of the Study:

  • To investigate the modulatory effect of laser stimulation on vascular smooth muscle contraction induced by mastoparan-7.
  • To determine the dose-dependent response of laser irradiation on G-protein-mediated contractions.

Main Methods:

  • Experiments were conducted on isolated, perfused Wistar rat tail arteries.
  • Vascular contraction was measured by changes in perfusion pressure under constant flow.
  • Laser irradiation was applied at increasing doses (10, 30, 110 mW) for 3 minutes per exposure.

Main Results:

  • Laser stimulation significantly decreased mastoparan-7-induced vascular smooth muscle contraction in a dose-dependent manner.
  • Half-maximal effective concentration values increased significantly with laser irradiation compared to controls.
  • Laser treatment inhibited calcium ion (Ca2+) influx from both intracellular and extracellular stores.

Conclusions:

  • Laser radiation effectively inhibits G-protein-mediated vascular smooth muscle contraction induced by mastoparan-7.
  • The inhibitory effect of laser stimulation is associated with reduced Ca2+ influx from intracellular and extracellular sources.