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Long-term dietary L-arginine supplementation increases endothelial nitric oxide synthase and vasoactive intestinal peptide immunoexpression in rat small intestine
Long-term dietary L-arginine supplementation increases endothelial nitric oxide synthase and vasoactive intestinal peptide immunoexpression in rat small intestine
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Long-term dietary L-arginine supplementation increases endothelial nitric oxide synthase and vasoactive intestinal peptide immunoexpression in rat small intestine
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Long-term dietary L-arginine supplementation increases endothelial nitric oxide synthase and vasoactive intestinal peptide immunoexpression in rat small intestine
Long-term dietary L-arginine supplementation increases endothelial nitric oxide synthase and vasoactive intestinal peptide immunoexpression in rat small intestine

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Long-term dietary L-arginine supplementation increases endothelial nitric oxide synthase and vasoactive intestinal peptide immunoexpression in rat small intestine
Long-term dietary L-arginine supplementation increases endothelial nitric oxide synthase and vasoactive intestinal peptide immunoexpression in rat small intestine
Journal Article

Long-term dietary L-arginine supplementation increases endothelial nitric oxide synthase and vasoactive intestinal peptide immunoexpression in rat small intestine

2014
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Overview
BACKGROUND AND AIMS: Nitric oxide (NO) and vasoactive intestinal polypeptide (VIP) are important intestinal neurotransmitters that coexist in the gut enteric nervous system and play an important role in intestinal physiology (e.g., absorption, motility, fluid secretion and smooth muscle relaxation). It is also known that cold exposure alters several aspects of gastrointestinal physiology and induces hyperphagia to meet increased metabolic demands, but there are no data regarding NO and VIP involvement in intestinal response during acclimation to cold. The objective of this study was to determine the influence of long-term L-arginine supplementation on the expression of the three isoforms of nitric oxide synthase (NOS) and VIP in small intestine of rats acclimated to room temperature or cold. METHODS: Animals (six per group) acclimated to room temperature (22 ± 1 °C) and cold (4 ± 1 °C), respectively, were treated with 2.25 % L-arginine, a substrate for NOSs, or with 0.01 % N ω-nitro-L-arginine methyl ester, an inhibitor of NOSs, for 45 days. The topographical distribution of VIP and NOSs expression in small intestine was studied by immunohistochemistry, and ImageJ software was used for semiquantitative densitometric analysis of their immunoexpression. RESULTS: Long-term dietary L-arginine supplementation increases VIP and NOSs immunoexpression at room temperature while at cold increases the endothelial NOS, inducible NOS and VIP but decrease neuronal NOS in rat small intestine. CONCLUSION: Our results demonstrate that long-term dietary L-arginine supplementation modulates NOSs and VIP immunoexpression in rat small intestine with respect to ambient temperature, pointing out the eNOS as a predominant NOS isoform with an immunoexpression pattern similar to VIP.
Publisher
Springer-Verlag,Springer Berlin Heidelberg,Springer,Springer Nature B.V
Subject

acclimation

/ Adaptation, Physiological

/ Adaptation, Physiological - drug effects

/ adverse effects

/ agonists

/ ambient temperature

/ Animals

/ antagonists & inhibitors

/ Arginine

/ Arginine - antagonists & inhibitors

/ Arginine - metabolism

/ Biological and medical sciences

/ Chemistry

/ Chemistry and Materials Science

/ cold

/ cold stress

/ Cold Temperature

/ Cold Temperature - adverse effects

/ computer software

/ Crosses, Genetic

/ cytology

/ densitometry

/ Dietary Supplements

/ drug effects

/ Enterocytes

/ Enterocytes - cytology

/ Enterocytes - drug effects

/ Enterocytes - metabolism

/ Enzyme Inhibitors

/ Enzyme Inhibitors - pharmacology

/ Feeding. Feeding behavior

/ Fundamental and applied biological sciences. Psychology

/ Immunohistochemistry

/ Interstitial Cells of Cajal

/ Interstitial Cells of Cajal - cytology

/ Interstitial Cells of Cajal - drug effects

/ Interstitial Cells of Cajal - metabolism

/ Intestinal Mucosa

/ Intestinal Mucosa - cytology

/ Intestinal Mucosa - drug effects

/ Intestinal Mucosa - metabolism

/ Intestine, Small

/ Intestine, Small - cytology

/ Intestine, Small - drug effects

/ Intestine, Small - metabolism

/ Male

/ metabolism

/ nervous system

/ neurotransmitters

/ NG-Nitroarginine Methyl Ester

/ NG-Nitroarginine Methyl Ester - pharmacology

/ nitric oxide

/ nitric oxide synthase

/ Nitric Oxide Synthase Type I

/ Nitric Oxide Synthase Type I - antagonists & inhibitors

/ Nitric Oxide Synthase Type I - metabolism

/ Nitric Oxide Synthase Type II

/ Nitric Oxide Synthase Type II - antagonists & inhibitors

/ Nitric Oxide Synthase Type II - chemistry

/ Nitric Oxide Synthase Type II - metabolism

/ Nitric Oxide Synthase Type III

/ Nitric Oxide Synthase Type III - antagonists & inhibitors

/ Nitric Oxide Synthase Type III - chemistry

/ Nitric Oxide Synthase Type III - metabolism

/ Nutrition

/ Original Contribution

/ overeating

/ pharmacology

/ Rats

/ secretion

/ small intestine

/ smooth muscle

/ Up-Regulation

/ Up-Regulation - drug effects

/ vasoactive intestinal peptide

/ Vasoactive Intestinal Peptide - agonists

/ Vasoactive Intestinal Peptide - metabolism

/ Vertebrates: anatomy and physiology, studies on body, several organs or systems