Research reportOverexpression of NMDAR2B in an inflammatory model of Alzheimer's disease: Modulation by NOS inhibitors

•Systemic inflammation leads to AD and this effect is mediated through NO.•Both nNOS and iNOS contribute to the progression of AD.•NMDAR2B subunits could be used as a measure for the progression of AD.

BackgroundAlzheimer's disease (AD) is a common form of age-related dementia, characterized by deposition of amyloid Aβ plaques, neuroinflammation and neurodegeneration. N-methyl-d-aspartate receptors (NMDAR) are postsynaptic glutamate receptors that play a role in memory formation and are targets for memantadine, an anti-AD drug. Nitric oxide (NO) signaling has been involved in both memory development through neuronal NO synthase (nNOS), and neuroinflammation through inducible NO synthase (iNOS) which mediates CNS inflammatory processes.AimTo study the expression of the NMDAR2B subunit in an inflammatory model of AD before and after treatment with NO modulators.Materials and methodsAD was induced in mice by a single dose of lipopolysaccharide (LPS). Behavioral tests for spatial and non-spatial memories and locomotor activity were performed to assess disease severity and progression. The effects of l-NAME (general NOS inhibitor), 1400W (iNOS inhibitor), diflunisal (systemic anti-inflammatory drug that does not cross the blood brain barrier), and l-arginine, the substrate for NOS was determined. Immunohistochemistry was done to confirm AD and brain lysates were tested for Aβ formation, levels of NMDAR2B subunits, and brain NO levels.ResultsSystemic LPS induced AD, as shown by cognitive impairment; increased levels of Aβ and concomitant increase in the brain NO concentrations. This was associated with overexpression of NMDAR2B. All tested drugs improved behavioral dysfunction, prevented Aβ formation and NMDAR overexpression, and lead to decrease in NO concentration in the brain. l-Arginine alone, however, did not produce similar improvements.ConclusionNMDAR2B subunits are overexpressed in an inflammatory model of AD and NO inhibitors ameliorate this expression.