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/Bcl-2 and cytochrome c and improved mitochondrial function in MI mice via activating the AMPK-PGC1α

) mouse models were used. Mice were administered with Met in an intragastric manner. We found

by regulating TRAF6 in DN. Material and methods: C57BL/6 mice were injected with streptozotocin to induce type 1

in DCM and to test the therapeutic effects of MD2 inhibitor C30 on DCM. Streptozotocin (STZ) was used

. It was shown that compounds 3, 5, and 8 increased the lifespan of mice in various hypoxia models.

spectroscopic data. The acute toxicity was studied. The LD50 values were 700 mg/kg for outbred albino mice. Tail

action on GABA-ergic neurotransmission in brains of outbred white mice. M-20 at a dose of 12 mg

the life span of mice undernormobaric hypoxia by 30% (P < 0.05) and, after injection of sodium

knockout mice exhibited decreased cardiac regenerative ability and heart function after neonatal apex

). The pharmacological effect of CAR was further evaluated in both LPS-stimulated macrophages and ALI mice model. Results

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