Altered dopamine signalling in chronic epigastric pain syndrome.


Journal

Journal of physiology and pharmacology : an official journal of the Polish Physiological Society
ISSN: 1899-1505
Titre abrégé: J Physiol Pharmacol
Pays: Poland
ID NLM: 9114501

Informations de publication

Date de publication:
Dec 2020
Historique:
received: 01 12 2020
accepted: 30 12 2020
entrez: 17 3 2021
pubmed: 18 3 2021
medline: 11 11 2021
Statut: ppublish

Résumé

Chronic epigastric pain syndrome (CEPS) is an important diagnostic problem, especially in patients without macroscopic and microscopic changes in gastric mucosa. The cause of this ailment is unclear. The aim of this study was the assessment of coexistence between symptoms of this syndrome and secretion level of dopamine (DA), as well as the efficacy of peripheral and central D2 receptors antagonist. Sixty depressive patients with CEPS occurring independently of the diet and with no Helicobacter pylori infection and 30 healthy subjects were enrolled in this study. Plasma DA and urinary homovanilic acid (HVA) concentration were measured by ELISA, and the mRNA expression of dopa decarboxylase (DDC) in gastric mucosa was evaluated by RT-PCR in 30 patients with CEPS and 30 controls. Severity of epigastric pain before and after 12 weeks 2 x 50 mg itopride or sulpiride treatment was evaluated using the modified 10-point Visual Analogue Scale. Higher average levels of plasma DA and urinary HVA levels in CEPS patients than controls 129.5 ± 22.0 versus 109.1 ± 18.4 pg/ml (p < 0.001) and 6.82 ± 1.55 versus 5.39 ± 1.04 mg/24 h, respectively were obtained. Moreover, the expression of DDC in gastric mucosa of CEPS patients was higher than in healthy subjects (p < 0.01). Sulpiride subsided epigastric pain in 73.3%, but itopride reduced it only in 6.6% of CEPS patients. We concluded that altered dopamine signalling may affect locally-and-centrally mediated chronic epigastric pain.

Identifiants

pubmed: 33727428
doi: 10.26402/jpp.2020.6.05
doi:

Substances chimiques

Benzamides 0
Benzyl Compounds 0
Dopamine Antagonists 0
Sulpiride 7MNE9M8287
itopride 81BMQ80QRL
Dopamine VTD58H1Z2X
Homovanillic Acid X77S6GMS36

Types de publication

Comparative Study Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Auteurs

C Chojnacki (C)

Department of Clinical Nutrition and Gastroenterological Diagnostics, Medical University, Lodz, Poland.

T Poplawski (T)

Department of Molecular Genetics, Faculty of Biology and Environmental Sciences, University of Lodz, Lodz, Poland.

J Blasiak (J)

Department of Molecular Genetics, Faculty of Biology and Environmental Sciences, University of Lodz, Lodz, Poland.

M Fila (M)

Department of Neurology, Polish Mother Memorial Hospital-Research Institute, Lodz, Poland.

P Konrad (P)

Department of Clinical Nutrition and Gastroenterological Diagnostics, Medical University, Lodz, Poland.

J Chojnacki (J)

Department of Clinical Nutrition and Gastroenterological Diagnostics, Medical University, Lodz, Poland. jan.chojnacki@umed.lodz.pl.

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Classifications MeSH