Sulphide impairment of substrate oxidation in rat colonocytes: a biochemical basis for ulcerative colitis?
WEW Roediger, A Duncan, O Kapaniris… - Clinical …, 1993 - portlandpress.com
WEW Roediger, A Duncan, O Kapaniris, S Millard
Clinical science, 1993•portlandpress.com1. Isolated colonic epithelial cells of the rat were incubated for 40 min with [6-14C] glucose
and n-[1-14C] batyrate in the presence of 0.1-2.0 mmol/l NaHS, a concentration range found
in the human colon. Metabolic products, 14CO2, acetoacetate, β-hydroxybutyrate and
lactate, were measured and injury to cells was judged by diminished production of
metabolites. 2. Oxidation of n-butyrate to CO2 and acetoacetate was reduced at 0.1 and 0.5
mmol/l NaHS, whereas glucose oxidation remained unimpaired. At 1.0-2.0 mmol/l NaHS, n …
and n-[1-14C] batyrate in the presence of 0.1-2.0 mmol/l NaHS, a concentration range found
in the human colon. Metabolic products, 14CO2, acetoacetate, β-hydroxybutyrate and
lactate, were measured and injury to cells was judged by diminished production of
metabolites. 2. Oxidation of n-butyrate to CO2 and acetoacetate was reduced at 0.1 and 0.5
mmol/l NaHS, whereas glucose oxidation remained unimpaired. At 1.0-2.0 mmol/l NaHS, n …
1. Isolated colonic epithelial cells of the rat were incubated for 40 min with [6-14C]glucose and n-[1-14C]batyrate in the presence of 0.1-2.0 mmol/l NaHS, a concentration range found in the human colon. Metabolic products, 14CO2, acetoacetate, β-hydroxybutyrate and lactate, were measured and injury to cells was judged by diminished production of metabolites.
2. Oxidation of n-butyrate to CO2 and acetoacetate was reduced at 0.1 and 0.5 mmol/l NaHS, whereas glucose oxidation remained unimpaired. At 1.0-2.0 mmol/l NaHS, n-butyrate and glucose oxidation were dose-dependently reduced at the same rate.
3. To bypass short-chain acyl-CoA dehydrogenase activity necessary for butyrate oxidation, ketogenesis from crotonate was measured in the presence of 1.0 mmol/l NaHS. Suppression by sulphide of ketogenesis from crotonate (−10.5 + 6.1%) compared with control conditions was not significant, whereas suppression of ketogenesis from n-butyrate (−36.00 + 5.14%) was signficant (P = <0.01). Inhibition of FAD-linked oxidation was more affected by NaHS than was NAD-linked oxidation.
4. L-Methionine (5.0 mmol/l) significantly redressed the impaired β-oxidation induced by NaHS. Methionine equally improved CO2 and ketone body production, suggesting a global reversal of the action of sulphide.
5. Sulphide-induced oxidative changes closely mirror the impairment of β-oxidation observed in colonocytes of patients with ulcerative colitis. A hypothesis for the disease process of ulcerative colitis is that sulphides may form persulphides with butyryl-CoA, which would inhibit cellular short-chain acyl-CoA dehydrogenase and β-oxidation to induce an energy-deficiency state in colonocytes and mucosal inflammation.
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