2020
DOI: 10.3390/ijms21062157
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Neurochemical Plasticity of nNOS-, VIP- and CART-Immunoreactive Neurons Following Prolonged Acetylsalicylic Acid Supplementation in the Porcine Jejunum

Abstract: Aspirin, also known as acetylsalicylic acid (ASA), is a commonly used anti-inflammatory drug that has analgesic and antipyretic properties. The side effects are well known, however, knowledge concerning its influence on gastric and intestinal innervation is limited. The enteric nervous system (ENS) innervates the whole gastrointestinal tract (GIT) and is comprised of more than one hundred million neurons. The capacity of neurons to adapt to microenvironmental influences, termed as an enteric neuronal plasticit… Show more

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Cited by 13 publications
(11 citation statements)
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“…In the pancreas, CART serves a physiological role in regulating both endocrine and exocrine pancreatic secretions ( 20 ). CART also regulates islet hormone secretion ( 21 ) and gastrointestinal tract motility ( 22 ). A previous study demonstrated that CART is positively associated with oxidative stress ( 23 ).…”
Section: Introductionmentioning
confidence: 99%
“…In the pancreas, CART serves a physiological role in regulating both endocrine and exocrine pancreatic secretions ( 20 ). CART also regulates islet hormone secretion ( 21 ) and gastrointestinal tract motility ( 22 ). A previous study demonstrated that CART is positively associated with oxidative stress ( 23 ).…”
Section: Introductionmentioning
confidence: 99%
“…It should be added that other toxic substances entering the gastrointestinal tract, such as bisphenol A, also cause significant changes in the expression of the same substances in the neurons of the jejunum [ 30 ]. Long-term use of aspirin also causes changes in the chemical phenotype of the neurons of the enteric nervous system of the porcine jejunum which confirms the adaptability of the enteric neurons to adverse factors and pathological conditions [ 36 ].…”
Section: Discussionmentioning
confidence: 91%
“…The jejunal sections were subjected to double fluorescence immunohistochemical staining to determine the phenotype of enteric neurons in experimental and control animals; these methods were the same as described in a previous paper [ 48 ]. In the first stage of the study, the slides were dried at room temperature for one hour and then washed in 0.1 M phosphate buffered saline (PBS, pH 7.4) for 3 × 10 min.…”
Section: Methodsmentioning
confidence: 99%