Astragaloside IV improves cognitive function in diabetic mice

Published on September 29, 2022

Imagine you’re trying to solve a complicated puzzle, but your brain is feeling foggy and sluggish. That’s how it feels for mice with diabetes when their cognitive function is impaired. But fear not! A traditional Chinese medicine called Astragaloside IV (AS-IV) may be the answer to sharpening their minds. AS-IV has special powers – it can reduce inflammation and fight off harmful molecules that cause oxidative stress. In a study, diabetic mice were given AS-IV over 8 weeks, and the results were astounding! Not only did the mice’s learning and memory improve, but their anxiety levels decreased as well. It turns out that AS-IV works its magic by activating a pathway called Nrf2/Keap1/HO-1/NQO1, which helps protect the brain from damage. By reducing oxidative stress and inflammation, AS-IV may be a promising treatment for diabetic cognitive impairment. So, if you want to delve deeper into this fascinating research and learn more about how AS-IV can boost brain power, check out the full article!

Although diabetic cognitive impairment is one of the most common complications of type 2 diabetes mellitus (T2DM), optimized therapeutic strategies are not available yet. Astragalosides IV (AS-IV) is a traditional Chinese medicine possessing diverse pharmacological properties including anti-inflammatory and antioxidant effects. However, the effects of AS-IV on diabetes-related cognitive impairment and its precise mechanisms remain largely unknown. T2DM mice, induced by a high-fat diet (HFD) and an intraperitoneal injection of low-dose streptozotocin (STZ) were administrated with AS-IV every other day for eight consecutive weeks. Learning and memory abilities were assessed subsequently using the Ymaze test and the anxious behavior was evaluated using an open field test. Then, the morphology and number of neurons and microglia were observed by HE staining or immunohistochemistry. Oxidative stress biomarkers and pro-inflammatory cytokines were determined using relevant kits. In addition, the expression levels of Nrf2, Keap1, HO-1, and NQO1 were determined by Western blot analyses. The results indicated that AS-IV administration significantly improved neuronal damage and cognitive deficit in T2DM mice. Meanwhile, oxidative stress and neuroinflammation were also ameliorated in T2DM mice, which might be attributed to the regulation of Nrf2/Keap1/HO-1/NQO1 pathway in T2DM mice. Taken together, these data suggested that AS-IV ameliorates cognitive impairment in T2DM mice by attenuating oxidative stress and neuroinflammation, possibly through modulating the Nrf2/Keap1/HO1/NQO1 pathway.

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