S U M M A R YThe simulated annealing method was applied to jointly invert gravity and resistivity data to obtain the geometry of the density/resistivity interfaces and subsurface electrical resistivity distribution. The results obtained from the inversions of synthetic data indicate that the joint inversion significantly improves the solution decreasing the ambiguity of the models. The method was applied to gravity and resistivity data carried out in Sinai (northwestern Egypt). The results obtained revealed the geometry of the water-bearing zone with thickness ranging from 80 to 180 m and of the limestone-bedrock interface dipping northwards.
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BackgroundSirtuin 1 (SIRT1) and sirtuin 3 (SIRT3) proteins have an important role in counteracting oxidative stress. Although diabetes and hypothyroidism (HT) are both characterized by oxidative stress, the mechanisms are not fully understood. This study investigated the effects of type 1 diabetes (T1D), type 2 diabetes (T2D), and HT on the expression levels of SIRT1, SIRT3, and manganese superoxide dismutase (SOD2).MethodsGene expression of SIRT1, SIRT3, and SOD2 was measured using real-time PCR. The protein expression of SOD2 and lipid peroxidation (thiobarbituric acid reactive substances) was measured by the TBARS Assay kit and enzyme-linked immunosorbent assay (ELISA) respectively.ResultsThe results showed that the SIRT1 and SIRT3 levels were lower in peripheral blood samples from patients with T1D, T2D, or HT than in healthy individuals. Interestingly, the mRNA and protein expression levels of SOD2 were higher in all three patient groups. Lipid peroxidation was higher in the patients with HT than in the healthy individuals.ConclusionsThese results indicate alterations in the expression levels of sirtuins and superoxide dismutase in diabetes and HT, which may be related, at least in part, to the oxidative stress. Identifying such alterations in those patients will pave the way towards the development of drugs to enhance SIRT1 and SIRT3 expression and their activity to prevent the damaging effect of oxidative stress.
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