Altered expression of neuronal nitric oxide synthase in the duodenum longitudinal muscle-myenteric plexus of obesity induced diabetes mouse: implications on enteric neurodegeneration

Biochem Biophys Res Commun. 2005 Dec 16;338(2):919-22. doi: 10.1016/j.bbrc.2005.10.039. Epub 2005 Oct 21.

Abstract

Type 2 diabetes caused by obesity shows autonomic neuropathy. Molecular mechanism involved in enteric neurodegeneration is not clear. Neuronal nitric oxide synthase (nNOS) is one of the important agents involved in gastrointestinal function. Therefore, expression of nNOS in the duodenum LM-MP of type 2 diabetes model mouse was studied. Real time RT-PCR analysis showed reduction in nNOS expression in male diabetic LM-MP compared to male control. In contrast, female diabetic LM-MP had high level of nNOS mRNA compared to female control. Western blot determination of LM-MP showed reduction in nNOS protein in male diabetic LM-MP and high level of nNOS in female diabetic LM-MP compared to their respective controls. Expression of nNOS observed by Western blot was further confirmed by nNOS immunostaining of the mouse duodenum. TUNEL staining of mouse duodenum showed apoptosis in male diabetic enteric neurons. These studies suggest that nNOS expression in LM-MP varies with gender during early stage of type 2 diabetes. In addition, reduced expression of nNOS is likely to contribute to apoptosis seen in the enteric neurons of male type 2 diabetic mice.

MeSH terms

  • Animals
  • Diabetes Mellitus, Type 2 / complications
  • Diabetes Mellitus, Type 2 / enzymology*
  • Disease Models, Animal*
  • Duodenal Diseases / enzymology
  • Duodenal Diseases / etiology
  • Duodenum / enzymology*
  • Duodenum / innervation
  • Female
  • Male
  • Mice
  • Muscle, Smooth / enzymology*
  • Muscle, Smooth / innervation
  • Myenteric Plexus / enzymology*
  • Neurodegenerative Diseases / enzymology
  • Neurodegenerative Diseases / etiology
  • Nitric Oxide Synthase Type I / metabolism*
  • Obesity / complications
  • Obesity / enzymology*
  • Sex Factors
  • Tissue Distribution

Substances

  • Nitric Oxide Synthase Type I