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Spinocerebellar ataxia type 2 Spinocerebellar ataxia type 2a genetic neurodegenerative disorder due to a CAG repeat expansion mutation in the ATXN2 gene coding for the protein ataxin-2 63 has been associated to oxidative stress, in particular due to alterations in the enzymatic activity of antioxidant enzymes including GSTs 64
This has similar or better absorption to the sublingual avenue, without the risk of most of the glutathione going to the stomach and being dissolved
Semaglutide primarily targets GLP-1 alone, while Tirzepatide combines GLP-1 and GIP receptor activity, giving it a broader incretin signalling profile
Hudson, M.E
DHT is converted from testosterone thanks to the enzyme known as 5-alpha reductase
Presented for research literature review only Papaseit E et al
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