IV therapy restores electrolytes while rehydrating the cells
[Google Scholar] Littler DR, Harrop SJ, Goodchild SC, et al
The selection of hepatotoxic agents i.e., acetaminophen, bisphenol A (BPA), aflatoxins, microcystins, heavy metals, alcohol, hepatitis B and C, and non-alcoholic fatty liver disease (NAFLD) progressing to non-alcoholic steatohepatitis (NASH)was based on their global prevalence, clinical relevance, and diverse mechanisms of hepatotoxicity.These agents encompass a wide range of pathways, including oxidative stress (BPA, microcystins), mitochondrial dysfunction (acetaminophen), immune activation (hepatitis B and C), and fibrosis (NASH and alcohol)
In vitro models of endothelial cell dysfunction The complexity of ECD, associated with the distinct triggers that can provoke it, has been untangled with the utilization of several in vitro models