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. 2020 Dec 18:2020:2624734.
doi: 10.1155/2020/2624734. eCollection 2020.

Magnesium Sulfate Attenuates Lethality and Oxidative Damage Induced by Different Models of Hypoxia in Mice

Affiliations

Magnesium Sulfate Attenuates Lethality and Oxidative Damage Induced by Different Models of Hypoxia in Mice

Hamidreza Mohammadi et al. Biomed Res Int. .

Abstract

Mg2+ is an important cation in our body. It is an essential cofactor for many enzymes. Despite many works, nothing is known about the protective effects of MgSO4 against hypoxia-induced lethality and oxidative damage in brain mitochondria. In this study, antihypoxic and antioxidative activities of MgSO4 were evaluated by three experimental models of induced hypoxia (asphyctic, haemic, and circulatory) in mice. Mitochondria protective effects of MgSO4 were evaluated in mouse brain after induction of different models of hypoxia. Antihypoxic activity was especially pronounced in asphyctic hypoxia, where MgSO4 at dose 600 mg/kg showed the same activity as phenytoin, which used as a positive control (P < 0.001). In the haemic model, MgSO4 at all used doses significantly prolonged latency of death. In circulatory hypoxia, MgSO4 (600 mg/kg) doubles the survival time. MgSO4 significantly decreased lipid peroxidation and protein carbonyl and improved mitochondrial function and glutathione content in brain mitochondria compared to the control groups. The results obtained in this study showed that MgSO4 administration has protective effects against lethality induced by different models of hypoxia and improves brain mitochondria oxidative damage.

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Conflict of interest statement

The authors declared no conflicts of interest.

Figures

Figure 1
Figure 1
Antihypoxic activities of different doses of MgSO4 in the asphyctic hypoxia method in mice. Data are expressed as mean ± SD (n = 8).
Figure 2
Figure 2
Antihypoxic activities of MgSO4 at different doses in induced haemic hypoxia in mice. Data are expressed as mean ± SD (n = 8); P < 0.05 and ∗∗P < 0.01 compared to control (NaNO2).
Figure 3
Figure 3
Antihypoxic activities of different doses of MgSO4 in circulatory-induced hypoxia in mice. Data are expressed as mean ± SD (n = 8); ns: not significant; ∗∗∗P < 0.001 compared to control (NaF).
Figure 4
Figure 4
Effect of different doses of MgSO4 and phenytoin on mitochondrial function after induced hypoxia by the asphyctic method. Values represented as mean ± SD (n = 8). P < 0.05 compared with the control group (NS).
Figure 5
Figure 5
Effect of different doses of MgSO4 on mitochondrial function after induced hypoxia by the haemic (NaNO2) method. Data are presented as mean ± SD (n = 8). P < 0.05 compared with the control group (NaNO2).
Figure 6
Figure 6
Effect of different doses of MgSO4 on mitochondrial function after induced hypoxia by the circulatory (NaF) method. Data are presented as mean ± SD (n = 8). P < 0.05 compared with the control group (NaF).

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