Far red/near infrared light-induced protection against cardiac ischemia and reperfusion injury remains intact under diabetic conditions and is independent of nitric oxide synthase

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Abstract

Far red/near-infrared light (NIR) promotes a wide range of biological effects including tissue protection but whether and how NIR is capable of acutely protecting myocardium against ischemia and reperfusion injury in vivo is not fully elucidated. Our previous work indicates that NIR exposure immediately before and during early reperfusion protects the myocardium against infarction through mechanisms that are nitric oxide (NO)-dependent. Here we tested the hypothesis that NIR elicits protection in a diabetic mouse model where other cardioprotective interventions such as pre- and postconditioning fail, and that the protection is independent of nitric oxide synthase (NOS). NIR reduced infarct size dose dependently. Importantly, NIR-induced protection was preserved in a diabetic mouse model (db/db) and during acute hyperglycemia, as well as in endothelial NOS-/- mice and in wild type mice treated with NOS inhibitor L-NAME. In in vitro experiments NIR light liberates NO from nitrosyl hemoglobin (HbNO) and nitrosyl myoglobin (MbNO) in a wavelength-(660-830 nm) and dose-dependent manner. Irradiation at 660 nm yields the highest release of NO, while at longer wavelengths a dramatic decrease of NO release can be observed. Similar wavelength dependence was observed for the protection of mice against cardiac ischemia and reperfusion injury in vivo. NIR-induced NO release from deoxymyoglobin in the presence of nitrite mildly inhibits respiration of isolated mitochondria after hypoxia. In summary, NIR applied during reperfusion protects the myocardium against infarction in an NO-dependent, but NOS-independent mechanisms, whereby mitochondria may be a target of NO released by NIR, leading to reduced reactive oxygen species generation during reperfusion. This unique mechanism preserves protection even during diabetes where other protective strategies fail. © 2014 Keszler, Brandal, Baumgardt, Ge, Pratt, Riess and Bienengraeber.

Figures

  • FIGURE 1 | The NIR-mediated cardioprotection is irradiance-dependent.
  • FIGURE 2 | The NIR-mediated cardioprotection is NOS-independent. The exposed heart of wild type and eNOS−/− mice was irradiated at 670 nm with 170 mW/cm2 power for 1 min during ischemia, and 4 min during reperfusion. Mice treated with L-NAME (10 mg/kg, administered 10 min prior occlusion) were also examined. Irradiation was equally protective in the case of control, L-NAME-treated, and eNOS−/− mice. Values are means ± SD, ∗p < 0.05 when compared to untreated control (CON).
  • FIGURE 3 | Wavelength-dependence of NIR-induced NO release is in accordance with wavelength dependence of cardioprotection. (A) A solution of HbNO or MbNO (10 µM in PBS, pH 7.4) was irradiated at various wavelengths with 10 mW/cm2 power for 1 min in the chamber of the NO analyzer. Formation of NO was on-line detected with ozone-based chemiluminescence. Maximum NO liberation was achieved at 660 nm irradiation with both heme nitrosyl compounds. Values are means ± SE, n = 3. (B) The exposed heart was irradiated at various wavelengths at170 mW/cm2 irradiance for 1 min during ischemia, and 4 min during reperfusion. Irradiation at 670 nm was the most cardioprotective. Values are means ± SD, ∗p < 0.05 when compared to untreated control (CON).
  • FIGURE 4 | NIR slows mitochondrial respiration in the presence of deoxymyoglobin and nitrite during reoxygenation. (A) Oxygen consumption of purified cardiac mitochondria was monitored with a Clarke-type oxygen electrode. At the beginning of ischemia, deoxyMb and sodium nitrite were added. During the second minute of ischemia before reoxygenation, mitochondria were exposed to NIR at 670 nm with 50 mW/cm2 irradiance. (B) NIR caused an NO-dependent increase of reoxygenation rate (corresponding to a decrease of respiration) in the presence of deoxyMb and nitrite. The effect was reversed with NO scavenger CPTIO. Values are means ± SD, n = 6, ∗p < 0.05 when compared to control, #p < 0.05 when compared to NIR treated mitochondria in the absence of CPTIO.
  • FIGURE 5 | NIR is cardioprotective in the presence of diabetes or hyperglycemia. The exposed heart of wild type, db/db, and hyperglycemic mice was irradiated at 670 nm with 170 mW/cm2 irradiance for 1 min during ischemia, and 4 min during reperfusion. Light exposure resulted in a similarly effective decrease of infarct size in all three cases. Values are means ± SD, ∗p < 0.05 when compared to untreated wild type.

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Keszler, A., Brandal, G., Baumgardt, S., Ge, Z. D., Pratt, P. F., Riess, M. L., & Bienengraeber, M. (2014). Far red/near infrared light-induced protection against cardiac ischemia and reperfusion injury remains intact under diabetic conditions and is independent of nitric oxide synthase. Frontiers in Physiology, 5 AUG. https://doi.org/10.3389/fphys.2014.00305

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