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Pol. Merkur. Lek (Pol. Med. J.), 2016, XL/238: 244-247 Maximize

Pol. Merkur. Lek (Pol. Med. J.), 2016, XL/238: 244-247

Title: Excretion and metabolism of dopamine in patients with functional dyspepsia 

Authors:  Wachowska-Kelly P, Stępień A, Romanowski M, Chojnacki C.

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SUMMARY IN POLISH & ENGLISH. FULL ARTICLE ONLY IN POLISH.

Excretion and metabolism of dopamine in patients with functional dyspepsia


Wachowska-Kelly P1, Stępień A2, Romanowski M2, Chojnacki C1.

Medical University in Lodz, Poland: 1Department of Clinical Nutrition and Gastroenterological Diagnostics; 2Department of Gastroenterology

Dopamine is one of major neurotransmitter in the central and peripheral nervous system. A significant amount of dopamine is also produced in the visceral nervous system and in gastrointestinal tract, where exhibits inhibitory activity on motility.
The aim of the study
was to assess the parameters of dopamine secretion and metabolism in patients with functional dyspepsia.
Material and methods
. The study was conducted in a group of 30 healthy subjects and 60 patients with functional dyspepsia (FD), that met the Rome Criteria III, for epigastric pain syndrome (EPS) and postprandial distress syndrome (PDS). The severity of dyspeptic symptoms was determined using a 10-point Visual-Analogue Scale (VAS). Fasting plasma concentration of dopamine (DA) and the contents of homovanillic acid (HVA) in the urine collection were determined by ELISA.
Results
. DA concentration in plasma was similar in both clinical forms FD (EPS – 55.6 pg/ml, in patients with PDS – 63.5 pg/ml, p>0.05). Urine excretion of HVA in patients with PDS – 6.63 mg/24 h (p<0.05) was higher than in heathy subjects – 5.65 mg/24 h (p<0.05) and those with EPS – 5.07 mg/24 h (p<0.001). In the group with PDS severity of dyspeptic symptoms showed a positive correlation with the DA concentration in plasma and HVA excretion in the urine.
Conclusion
. Increased secretion of DA may play a significant role in the pathogenesis of PDS.

Key words: functional dyspepsia, dopamine, dopamine receptors

Pol Med J, 2016; XL (238); 244–247