Nitric oxide (NO) is now known as an endogenous signaling molecule and involved in the various physiological signaling such as control of blood pressure. NO has gaseous property and short half-life due to susceptibility to oxidation under ambient conditions, so that it is difficult to handle it in biological experiments directly. NO donor compounds which release NO under physiological conditions have been instead developed, and photocontrollable NO releaser, that is caged NOs, are also developed which are advantageous for treatment with NO in a spatiotemporally controlled manner. We recently developed caged NOs and adopted them to cellular, tissue, and in vivo experiments. One of our caged NO, Flu-DNB, released NO by NIR fs-pulse laser irradiation, and induced blood vessel response in a living mouse brain, and another one, NOBL-1, released NO by blue light, and succeeded to induce relaxation responses in a vessel tissue strip. These compounds would be useful for the investigation of NO biology and also for the NO-related therapeutic research.
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