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Interestingly, ursodeoxycholic acid, the only treatment approved by the Food and Drug Administration for the treatment of primary biliary cirrhosis, a chronic cholestatic disorder, was shown to prevent the fall in GCL expression during chronic cholestasis (Serviddio et al., 2004) and increase GCL expression in cultured rat hepatocytes (Mitsuyoshi et al., 1999)

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investigated the effects of fucoidan obtained from Laminaria japonica on the immune response and intestinal microflora in a mouse model of immunosuppressant-induced immune disorder (166)

Its core function is to supply a bioavailable form of L-Carnitine that crosses the blood-brain barrier more efficiently, supporting neurological health, energy metabolism, and age-related cognitive decline
