Key result
Exposure to ionizing radiation in minipigs caused selective IGF-1 resistance, which was associated with heart hemorrhages, poor prognosis, and endothelial dysfunction.
Selective IGF-1 resistance is a novel mechanism of radiation injury that may contribute to hemostatic disorders and heart hemorrhages, particularly relevant for individuals with low IGF-1 activity.
IGF-1 resistance was associated with heart hemorrhages and mortality in irradiated minipigs; leaves open whether modulation affects bleeding risk in humans.
Although bone marrow aplasia has been considered for the past decades as the major contributor of radiation-induced blood disorders, cytopenias alone are insufficient to explain differences in the prevalence of bleeding. In this study, the minipig was used as a novel preclinical model of hematopoietic acute radiation syndrome to assess if factors other than platelet counts correlated with bleeding and survival. We sought to determine whether radiation affected the insulin-like growth factor-1 (IGF-1) pathway, a growth hormone with cardiovascular and radioprotective features. Gottingen and Sinclair minipigs were exposed to ionizing radiation at hematopoietic doses. The smaller Gottingen minipig strain was more sensitive to radiation; differences in IGF-1 levels were minimal, suggesting that increased sensitivity could depend on weak response to the hormone. Radiation caused IGF-1 selective resistance by inhibiting the anti-inflammatory anti-oxidative stress IRS/PI3K/Akt but not the pro-inflammatory MAPK kinase pathway, shifting IGF-1 signaling towards a pro-oxidant, pro-inflammatory environment. Selective IGF-1 resistance associated with hemorrhages in the heart, poor prognosis, increase in C-reactive protein and NADPH oxidase 2, uncoupling of endothelial nitric oxide synthase, inhibition of nitric oxide (NO) synthesis and imbalance between the vasodilator NO and the vasoconstrictor endothelin-1 molecules. Selective IGF-1 resistance is a novel mechanism of radiation injury, associated with a vicious cycle amplifying reactive oxygen species-induced damage, inflammation and endothelial dysfunction. In the presence of thrombocytopenia, selective inhibition of IGF-1 cardioprotective function may contribute to the development of hemostatic disorders. This finding may be particularly relevant for individuals with low IGF-1 activity, such as the elderly or those with cardiometabolic dysfunctions.
No takes yet. Share an insight, caveat, or question.
Kenchegowda et al. (2018) studied Hematopoietic acute radiation syndrome. Ionizing radiation was evaluated on IGF-1 pathway response, heart hemorrhages, and survival. Exposure to ionizing radiation in minipigs caused selective IGF-1 resistance, which was associated with heart hemorrhages, poor prognosis, and endothelial dysfunction.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: