P1 Effects of N-acetyl cysteine treatment on rats treated with a rich fructose diet: reversal or prevention?

Authors

  • María Cecilia Castro Center for Experimental and Applied Endocrinology (CENEXA), National University of La Plata (UNLP)-National Council for Scientific and Technical Research (CONICET), La Plata, Province of Buenos Aires, Argentina
  • Hernán Gonzalo Villagarcía Center for Experimental and Applied Endocrinology (CENEXA), National University of La Plata (UNLP)-National Council for Scientific and Technical Research (CONICET), La Plata, Province of Buenos Aires, Argentina
  • Ada Paula Nazar Center for Experimental and Applied Endocrinology (CENEXA), National University of La Plata (UNLP)-National Council for Scientific and Technical Research (CONICET), La Plata, Province of Buenos Aires, Argentina
  • María Laura Massa Center for Experimental and Applied Endocrinology (CENEXA), National University of La Plata (UNLP)-National Council for Scientific and Technical Research (CONICET), La Plata, Province of Buenos Aires, Argentina
  • Flavio Francini Center for Experimental and Applied Endocrinology (CENEXA), National University of La Plata (UNLP)-National Council for Scientific and Technical Research (CONICET), La Plata, Province of Buenos Aires, Argentina

DOI:

https://doi.org/10.47196/diab.v54i3Sup.382

Keywords:

treatment, n-acetylcysteine, rich fructose diet

Abstract

Introduction: Fructose overload promotes oxidative stress (OE) that induces metabolic damage, hepatic IR and local inflammatory response, alterations similar to those observed in human MS. NAC (N-acetyl-cysteine) has antioxidant capacity, provides substrates for the synthesis of GSH and has a high absorption rate at liver.

Objectives: to study the effects of the administration of NAC (orally and i.p.) at different doses, on endocrine-metabolic alterations induced by a fructose rich diet.

Materials and methods: 60-day-old male Sprague Dawley rats were divided into 6 groups and fed 21 days ad libitum. Control group received a standard commercial diet and tap water; fructose (F) group had access to a standard commercial diet plus 10% fructose in the drinking water. NAC treatment: it was administered in the drinking water together with fructose ensuring a daily dose of 25 mg / day (FN25), 1 g / l and 2 g / l (FN1 and FN2) were also tested for 21 days and i.p. 50 mg / kg in saline solution the last 5 days of treatment (FN50). Once the treatment was completed, the animals were sacrificed and serum glucose, triglyceridemia, total cholesterol and HDL, AST, ALT, uric acid and serum TBARS were determined and the glycemia-triglyceridemia (Gly-TG), triglyceridemia / HDL (TG / HDL) and AST / ALT indexes were calculated. At liver level, activity of the enzymes glucokinase (GQ) and fructokinase (FQ) was determined, as well as the glycogen content.

Results: At the serum level, F animals presented higher triglyceridemia and Gly-TG and TG / HDL indexes and a significant increase in FQ activity in the liver. FN2 treatment reversed triglyceridemia levels and FN50 group presented significant
decreases in triglyceridemia and both indexes. NAC significantly decreased GQ activity in FN2 and FN50 groups, without significant differences in the rest of the determinations. The following table shows the results of serum parameters. Values represent means ± SEM. n = 8. * p <0.05 vs C; #p <0.05 vs F.

Conclusions: fructose induced an increase in serum triglyceride levels, Gly-TG and TG / HDL indexes and an increase in FQ activity. The results obtained clearly show that the administration of NAC is effective both in preventing and reversing the observed alterations. It remains to determine the molecular mechanisms of action of NAC to achieve the mentioned effects.

Published

2023-01-10

How to Cite

Castro, M. C., Villagarcía, H. G., Nazar, A. P., Massa, M. L., & Francini, F. (2023). P1 Effects of N-acetyl cysteine treatment on rats treated with a rich fructose diet: reversal or prevention?. Journal of the Argentine Society of Diabetes, 54(3Sup), 106–106. https://doi.org/10.47196/diab.v54i3Sup.382

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