Abstract

Several studies have investigated the effect of photo-mediated ultrasound therapy (PUT) on the treatment of neovascularization. This study explores the impact of PUT on the release of the vasoactive agents nitric oxide (NO) and prostacyclin (PGI2) from the endothelial cells in an in vitro blood vessel model. In this study, an in vitro vessel model containing RF/6A chorioretinal endothelial cells was used. The vessels were treated with ultrasound-only (0.5, 1.0, 1.5 and 2.0 MPa peak negative pressure at 0.5 MHz with 10% duty cycle), laser-only (5, 10, 15 and 20 mJ/cm2 at 532 nm with a pulse width of 5 ns), and synchronized laser and ultrasound (PUT) treatments. Passive cavitation detection was used to determine the cavitation activities during treatment. The levels of NO and PGI2 generally increased when the applied ultrasound pressure and laser fluence were low. The increases in NO and PGI2 levels were significantly reduced by 37.2% and 42.7%, respectively, from 0.5 to 1.5 MPa when only ultrasound was applied. The increase in NO was significantly reduced by 89.5% from 5 to 20 mJ/cm2, when only the laser was used. In the PUT group, for 10 mJ/cm2 laser fluence, the release of NO decreased by 76.8% from 0.1 to 1 MPa ultrasound pressure. For 0.5 MPa ultrasound pressure in the PUT group, the release of PGI2 started to decrease by 144% from 15 to 20 mJ/cm2 laser fluence. The decreases in NO and PGI2 levels coincided with the increased cavitation activities in each group. In conclusion, PUT can induce a significant reduction in the release of NO and PGI2 in comparison with ultrasound-only and laser-only treatments.

Highlights

  • Introduction published maps and institutional affilPhoto-mediated ultrasound therapy (PUT) is a non-invasive technique based on photoacoustic cavitation produced by applying ultrasound bursts and laser pulses synchronously [1–4]

  • This study provides an understanding of the release of PGI2 and nitric oxide (NO) when treating with ultrasound-only, laser-only, and PUT

  • As PUT was already shown to be capable of shutting the blood vessels, this study focuses on understanding the effects on the release of NO and PGI2 as they are vasoactive agents [4]

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Summary

Introduction

The main mechanism of PUT is enhanced cavitation activity in the targeted vessels [9–16]. The enhanced cavitation activity can induce strong mechanical stresses in the vessels. These stresses directly influence the physiological functions of blood vessels by iations

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