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There is a beneficial effect in the -lipoic-acid-treated cohort on secondary end points, including the NIS

Compounds absorbed here enter systemic circulation without passing through the hepatic portal system

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Reduced exposure to stomach acid

To this first category belong mouse models of maternal respiratory infection with influenza virus and maternal immune activation (MIA) with either polyinosine/cytosine (poly(I:C), a synthetic, double-stranded RNA that evokes an antiviral-like immune reaction), or lipopolysaccharide (LPS, which evokes an antibacterial-like immune reaction) [31]