Nitric oxide synthesis in patients with infective gastroenteritis

Citation
P. Forte et al., Nitric oxide synthesis in patients with infective gastroenteritis, GUT, 45(3), 1999, pp. 355-361
Citations number
68
Categorie Soggetti
Gastroenerology and Hepatology","da verificare
Journal title
GUT
ISSN journal
00175749 → ACNP
Volume
45
Issue
3
Year of publication
1999
Pages
355 - 361
Database
ISI
SICI code
0017-5749(199909)45:3<355:NOSIPW>2.0.ZU;2-C
Abstract
Background-There is evidence that endogenous nitrate synthesis is notably i ncreased in patients with infective gastroenteritis. Aims-To determine whether this is due to nitric oxide (NO) production via t he L-arginine/NO pathway. Methods-Seven male patients with community acquired bacterial gastroenterit is and 15 healthy male volunteers participated in this study, All patients had stool culture positive infective gastroenteritis. A bolus of 200 mg L-[ N-15](2)-arginine was administered intravenously after an overnight fast. U rine was collected for the next 36 hours. Urinary [N-15:N-14]nitrate ratio was assessed by dry combustion in an isotope ratio mass spectrometer. Results-Mean 36 hour total urinary nitrate excretion in the gastroenteritis group was 5157 (577) mu mol compared with 2594 (234) mu mol in the control group (p<0.001). Thirty six hour urinary [N-15]nitrate excretion was consi derably higher in the gastroenteritis group compared with the control group (13782 (1665) versus 1698 (98) eta mol; p<0.001). These values represent 1 .129 (0.139)% and 0.138 (0.007)% of [N-15]nitrogen administered (p<0.001), respectively. Corrected 36 hour urinary [N-15]nitrate excretion for urinary creatinine was also significantly higher in the patient compared with the control group (1934 (221) versus 303 (35) eta mol/mmol; p<0.001). Conclusion-Results show notably enhanced nitrate synthesis due to increased activity of the L-arginine/NO pathway in patients with infective gastroent eritis.