Role of opsins and light or heat activated transient receptor potential ion channels in the mechanisms of photobiomodulation and infrared therapy

Sulbha K. Sharma , Sakshi Sardana , Michael R. Hamblin
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引用次数: 3

Abstract

Photobiomodulation (otherwise known as low level light therapy) is an emerging approach for treating many diseases and conditions such as pain, inflammation, wound healing, brain disorders, hair regrowth etc. The light used in this therapy generally lies in the red and near-infrared spectral regions. Despite many positive studies for treating different conditions, this therapy still faces some skepticism, which has prevented its widespread adoption in clinics. The main reasons behind this skepticism are the lack of comprehensive information about the molecular, cellular, and tissular mechanisms of action, which underpin the positive effects of photobiomodulation. Moreover, there is also another therapeutic application using longer wavelength infrared radiation, involving either infrared saunas or heat lamps which are powered by electricity, as well as infrared emitting textiles and garments which are solely powered by the wearer's own body heat. In recent years, much knowledge has been gained about the mechanism of action underlying these treatments, which will be summarized in this review. There are three broad classes of primary chromophores, which have so far been identified. One is mitochondrial cytochromes (including cytochrome c oxidase), another is opsins and light or heat-sensitive calcium ion channels, and a third is nanostructured water clusters. Light sensitive ion channels are activated by the absorption of light by the chromophore proteins, opsin-3 and opsin-4, while mitochondrial chromophores are activated by red or near-infra red (NIR) light up to about 850 nm. However NIR light at 980 nm or longer wavelengths can activate transient receptor potential (TRP) ion channels, probably after being absorbed by nanostructured water clusters. Heat-activated TRP channels undergo a conformational change triggered by only small temperature changes. Here we will discuss the role of opsins and light or heat activated TRP channels in the mechanism of photobiomodulation and infrared therapy.

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视蛋白和光或热激活的瞬时受体电位离子通道在光生物调节和红外治疗机制中的作用
光生物调节(也被称为低水平光疗法)是一种新兴的方法,用于治疗许多疾病和条件,如疼痛,炎症,伤口愈合,脑部疾病,头发再生等。在这种治疗中使用的光通常位于红色和近红外光谱区域。尽管在治疗不同疾病方面有许多积极的研究,但这种疗法仍然面临一些质疑,这阻碍了它在诊所的广泛采用。这种怀疑背后的主要原因是缺乏关于分子、细胞和组织作用机制的全面信息,这些机制支撑着光生物调节的积极作用。此外,还有另一种使用较长波长的红外辐射的治疗应用,包括由电力供电的红外桑拿或热灯,以及仅由穿戴者自身热量供电的红外发射纺织品和服装。近年来,人们对这些治疗方法的作用机制有了很多了解,本文将对此进行综述。到目前为止已经确定的原发色团有三大类。一种是线粒体细胞色素(包括细胞色素c氧化酶),另一种是视蛋白和对光或热敏的钙离子通道,第三种是纳米结构的水簇。光敏离子通道被发色团蛋白,视蛋白-3和视蛋白-4的光吸收激活,而线粒体发色团被高达850 nm的红光或近红外(NIR)光激活。然而,980 nm或更长的近红外光可能在被纳米结构的水团吸收后激活瞬时受体电位(TRP)离子通道。热激活TRP通道仅由微小的温度变化触发构象变化。本文将讨论视蛋白和光或热激活的TRP通道在光生物调节和红外治疗中的作用。
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