Diabetes-Related Induction of the Heme Oxygenase System and Enhanced Colocalization of Heme Oxygenase 1 and 2 with Neuronal Nitric Oxide Synthase in Myenteric Neurons of Different Intestinal Segments
Autor: | Lalitha Chandrakumar, Nikolett Bódi, Diána Mezei, Zita Szalai, Mária Bagyánszki |
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Rok vydání: | 2017 |
Předmět: |
Male
0301 basic medicine Aging medicine.medical_specialty Article Subject Myenteric Plexus Enzyme-Linked Immunosorbent Assay Ileum Endogeny Nitric Oxide Synthase Type I Biology medicine.disease_cause Biochemistry Diabetes Mellitus Experimental 03 medical and health sciences 0302 clinical medicine Nitrergic Neurons Internal medicine medicine Animals Rats Wistar lcsh:QH573-671 Myenteric plexus lcsh:Cytology Colocalization Cell Biology General Medicine Immunohistochemistry Rats Intestines Heme oxygenase 030104 developmental biology Endocrinology medicine.anatomical_structure nervous system 030220 oncology & carcinogenesis Heme Oxygenase (Decyclizing) Duodenum Nitrergic Neuron Oxidative stress Research Article |
Zdroj: | Oxidative Medicine and Cellular Longevity, Vol 2017 (2017) Oxidative Medicine and Cellular Longevity |
ISSN: | 1942-0994 1942-0900 |
DOI: | 10.1155/2017/1890512 |
Popis: | Increase in hyperglycaemia-induced oxidative stress and decreased effectiveness of endogenous defense mechanisms plays an essential role in the initiation of diabetes-related neuropathy. We demonstrated that nitrergic myenteric neurons display different susceptibilities to diabetic damage in different gut segments. Therefore, we aim to reveal the gut segment-specific differences in the expression of heme oxygenase (HO) isoforms and the colocalization of these antioxidants with neuronal nitric oxide synthase (nNOS) in myenteric neurons. After ten weeks, samples from the duodenum, ileum, and colon of control and streptozotocin-induced diabetic rats were processed for double-labelling fluorescent immunohistochemistry and ELISA. The number of both HO-immunoreactive and nNOS/HO-immunoreactive myenteric neurons was the lowest in the ileal and the highest in the colonic ganglia of controls; it increased the most extensively in the ileum and was also elevated in the colon of diabetics. Although the total number of nitrergic neurons decreased in all segments, the proportion of nNOS-immunoreactive neurons colocalizing with HOs was enhanced robustly in the ileum and colon of diabetics. We presume that those nitrergic neurons which do not colocalize with HOs are the most seriously affected by diabetic damage. Therefore, the regional induction of the HO system is strongly correlated with diabetes-related region-specific nitrergic neuropathy. |
Databáze: | OpenAIRE |
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