Mitochondria play a crucial role in tubular injury in diabetic kidney disease (DKD). MitoQ is a mitochondria-targeted antioxidant that exerts protective effects in diabetic mice, but the mechanism underlying these effects is not clear. We demonstrated that mitochondrial abnormalities, such as defective mitophagy, mitochondrial reactive oxygen species (ROS) overexpression and mitochondrial fragmentation, occurred in the tubular cells of db/db mice, accompanied by reduced PINK and Parkin expression and increased apoptosis. These changes were partially reversed following an intraperitoneal injection of mitoQ. High glucose (HG) also induces deficient mitophagy, mitochondrial dysfunction and apoptosis in HK-2 cells, changes that were reversed by mitoQ. Moreover, mitoQ restored the expression, activity and translocation of HG-induced NF-E2-related factor 2 (Nrf2) and inhibited the expression of Kelch-like ECH-associated protein (Keap1), as well as the interaction between Nrf2 and Keap1. The reduced PINK and Parkin expression noted in HK-2 cells subjected to HG exposure was partially restored by mitoQ. This effect was abolished by Nrf2 siRNA and augmented by Keap1 siRNA. Transfection with Nrf2 siRNA or PINK siRNA in HK-2 cells exposed to HG conditions partially blocked the effects of mitoQ on mitophagy and tubular damage. These results suggest that mitoQ exerts beneficial effects on tubular injury in DKD via mitophagy and that mitochondrial quality control is mediated by Nrf2/PINK.
Tough hydrogels, polymeric network structures with excellent mechanical properties (such as high stretchability and toughness), are emerging soft materials. Despite their remarkably mechanical features, tough hydrogels exhibit two flaws (freezing around the icing temperatures of water and drying under arid conditions). Inspired by cryoprotectants (CPAs) used in the inhibition of the icing of water in biological samples, a versatile and straightforward method is reported to fabricate extreme anti-freezing, non-drying CPA-based organohydrogels with long-term stability by partially displacing water molecules within the pre-fabricated hydrogels. CPA-based Ca-alginate/polyacrylamide (PAAm) tough hydrogels were successfully fabricated with glycerol, glycol, and sorbitol. The CPA-based organohydrogels remain unfrozen and mechanically flexible even up to -70 °C and are stable under ambient conditions or even vacuum.
We demonstrate a
facile and universal strategy in the fabrication of dual-cross-linked
(DC) single network hydrogels with high toughness, “nonswellability”,
rapid self-healing, and versatile adhesiveness based on polymer–tannic
acid (TA) multiple hydrogen bonds. Two widely used hydrogels, physically
cross-linked poly(vinyl alcohol) and chemically cross-linked polyacrylamide,
have been transformed to TA-based DC hydrogels by dipping the corresponding
aerogels into TA solution. The second cross-link via multiple polymer–TA
hydrogen bonds effectively suppresses the crack propagation, resulting
in both DC gels with high mechanical strength. But these two TA-based
DC hydrogels go through different deformation mechanisms during the
stretching based on analyzing their stress–strain curves using
the Mooney–Rivlin equation. Moreover, these DC hydrogels are
swelling-resistant, with strong toughness, good self-recoverability,
rapid self-healing, and versatile adhesiveness. This work provides
a simple route to fabricate multifunctional DC hydrogels, hopefully
promoting their applications as biomedical materials.
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