Mitochondrial NAD(P)+ transhydrogenase is unevenly distributed in different brain regions, and its loss causes depressive-like behavior and motor dysfunction in mice.

Abstract

Abstract—NAD(P)+ transhydrogenase (NNT) links redox states of the mitochondrial NAD(H) and NADP(H) via a

reaction coupled to proton-motive force across the inner mitochondrial membrane. NNT is believed to be ubiqui- tously present in mammalian cells, but its expression may vary substantially in different tissues. The present

study investigated the tissue distribution and possible roles of NNT in the mouse brain. The pons exhibited high NNT expression/activity, and immunohistochemistry revealed intense NNT labeling in neurons from brainstem nuclei. In some of these regions, neuronal NNT labeling was strongly colocalized with enzymes involved in the biosynthesis of 5-hydroxytryptamine (5-HT) and nitric oxide (

NO), which directly or indirectly require NADPH. Behavioral tests were performed in mice lacking NNT activity (Nnt/, mice carrying the mutated NntC57BL/6J allele from the C57BL/6J strain) and the Nnt+/+ controls. Our data demonstrated that aged Nnt/ mice (18–20 months old), but not adult mice (3–4 months old), showed an increased immobility time in the tail suspension test that was reversed by fluoxetine treatment, providing evidence of depressive-like behavior in these mice. Aged Nnt/ mice also exhibited behavioral changes and impaired locomotor activity in the open field and rotarod tests. Despite the colocalization between NNT and

NO synthase, the S-nitrosation and cGMP levels were independent of the Nnt

genotype. Taken together, our results indicated that NNT is unevenly distributed throughout the brain and asso- ciated with 5-THergic and

NOergic neurons. The lack of NNT led to alterations in brain functions related to mood and motor behavior/performance in aged mice.