» Articles » PMID: 25705628

Myosin Va but Not NNOSα is Significantly Reduced in Jejunal Musculomotor Nerve Terminals in Diabetes Mellitus

Overview
Specialty General Medicine
Date 2015 Feb 24
PMID 25705628
Citations 11
Authors
Affiliations
Soon will be listed here.
Abstract

Nitric oxide (NO) mediated slow inhibitory junction potential and mechanical relaxation after electrical field stimulation (EFS) is impaired in diabetes mellitus. Externally added NO donor restore nitrergic function, indicating that this reduction result from diminution of NO synthesis within the pre-junctional nerve terminals. The present study aimed to investigate two specific aims that may potentially provide pathophysiological insights into diabetic nitrergic neuropathy. Specifically, alteration in nNOSα contents within jejunal nerve terminals and a local subcortical transporter myosin Va was tested 16 weeks after induction of diabetes by low dose streptozotocin (STZ) in male Wistar rats. The results show that diabetic rats, in contrast to vehicle treated animals, have: (a) nearly absent myosin Va expression in nerve terminals of axons innervating smooth muscles and (b) significant decrease of myosin Va in neuronal soma of myenteric plexus. In contrast, nNOSα staining in diabetic jejunum neuromuscular strips showed near intact expression in neuronal cell bodies. The space occupancy of nitrergic nerve fibers was comparable between groups. Normal concentration of nNOSα was visualized within a majority of nitrergic terminals in diabetes, suggesting intact axonal transport of nNOSα to distant nerve terminals. These results reveal the dissociation between presences of nNOSα in the nerve terminals but deficiency of its transporter myosin Va in the jejunum of diabetic rats. This significant observation of reduced motor protein myosin Va within jejunal nerve terminals may potentially explain impairment of pre-junctional NO synthesis during EFS of diabetic gut neuromuscular strips despite presence of the nitrergic synthetic enzyme nNOSα.

Citing Articles

Efficiency of Biobran/MGN-3, an Arabinoxylan Rice Bran, in Attenuating Diabetes-Induced Cognitive Impairment of the Hippocampus via Oxidative Stress and IR/Akt/NF-B in Rats.

Abdou H, Hamaad F, Elmageed G, Ghoneum M Evid Based Complement Alternat Med. 2023; 2023:8248576.

PMID: 37501860 PMC: 10371599. DOI: 10.1155/2023/8248576.


Akt phosphorylation of neuronal nitric oxide synthase regulates gastrointestinal motility in mouse ileum.

Guerra D, Bok R, Vyas V, Orlicky D, Lorca R, Hurt K Proc Natl Acad Sci U S A. 2019; 116(35):17541-17546.

PMID: 31405982 PMC: 6717252. DOI: 10.1073/pnas.1905902116.


Time-dependent functional, morphological, and molecular changes in diabetic bladder dysfunction in streptozotocin-induced diabetic mice.

Yang X, Wang J, Rui-Wang , Xu Y, Chen F, Tang L Neurourol Urodyn. 2019; 38(5):1266-1277.

PMID: 31006139 PMC: 6850069. DOI: 10.1002/nau.24008.


Effect of Hyperglycemia on Purinergic and Nitrergic Inhibitory Neuromuscular Transmission in the Antrum of the Stomach: Implications for Fast Gastric Emptying.

He X, Guo Y, Goyal R Front Med (Lausanne). 2018; 5:1.

PMID: 29410956 PMC: 5787141. DOI: 10.3389/fmed.2018.00001.


Axonal transport in a peripheral diabetic neuropathy model: sex-dimorphic features.

Pesaresi M, Giatti S, Spezzano R, Romano S, Diviccaro S, Borsello T Biol Sex Differ. 2018; 9(1):6.

PMID: 29351809 PMC: 5775621. DOI: 10.1186/s13293-018-0164-z.


References
1.
LIKE A, Rossini A . Streptozotocin-induced pancreatic insulitis: new model of diabetes mellitus. Science. 1976; 193(4251):415-7. DOI: 10.1126/science.180605. View

2.
Hoffman P, Lasek R . The slow component of axonal transport. Identification of major structural polypeptides of the axon and their generality among mammalian neurons. J Cell Biol. 1975; 66(2):351-66. PMC: 2109569. DOI: 10.1083/jcb.66.2.351. View

3.
He C, Soffer E, Ferris C, Walsh R, Szurszewski J, Farrugia G . Loss of interstitial cells of cajal and inhibitory innervation in insulin-dependent diabetes. Gastroenterology. 2001; 121(2):427-34. DOI: 10.1053/gast.2001.26264. View

4.
Grover M, Farrugia G, Lurken M, Bernard C, Faussone-Pellegrini M, Smyrk T . Cellular changes in diabetic and idiopathic gastroparesis. Gastroenterology. 2011; 140(5):1575-85.e8. PMC: 3081914. DOI: 10.1053/j.gastro.2011.01.046. View

5.
Edstrom A, Edstrom J, Hokfelt T . Sedimentation analysis of ribonucleic acid extracted from isolated Mauthner nerve fibre components. J Neurochem. 1969; 16(1):53-66. DOI: 10.1111/j.1471-4159.1969.tb10343.x. View