In vitro inhibition of glucose transport across the intestinal membrane of mice exposed to trivalent chromium.

Tóm tắt

Background: Trivalent chromium (Cr3+) supplementation has been used in the management of type-2 diabetes mellitus and the small intestine plays significant role in glucose homeostasis. However, there is dearth of information on the glucose absorption ability of normal gut during Cr3+ exposure. In this study, we investigated the effect of Cr3+ exposure in the absorption of glucose in the normal gut.

Methodology: Thirty male slc:ddY mice (26.2 ± 1.1 g) were randomly and equally assigned to three groups: Group 1 (control) received drinking water while animals in groups 2 and 3 received 10 and 100 ppm Cr3+ respectively for 12 weeks through drinking water. Thereafter, they were sacrificed and their intestines excised, rinsed with ice-cold Ringer solution (RS) and nine everted-sacs were made, with addition of 200 µL RS. The sacs were incubated for 1 hour in 5 mL glucose-free RS and glucose concentrations were determined by spectrophotometry. Transmural potential change (PΔt) was assessed using the short-circuit currents. Data were analysed by one-way ANOVA and p< 0.05 was considered significant.

Results: A significant decrease in glucose concentration at the distal jejunum of the serosa in test groups compared with control was observed. The mucosa glucose concentration was elevated at the same region compared with control. The PΔt across the membrane reduced significantly at both the distal jejunum and ileum of Cr3+exposed groups compared with control

Conclusion: It may be concluded that Cr3+ exposure reduced intestinal glucose transport which might probably be a mechanism explored during management of diabetes.

Keywords: Glucose transport, in vitro, trivalent chromium, transmural membrane, mice

Résumé
Contexte: La supplémentation en chrome trivalent (Cr3+) a été utilisée dans la prise en charge du diabète de type 2 et l’intestin grêle joue un rôle important dans l’homéostasie du glucose. Cependant, il ya une pénurie d’informations sur la capacité d’absorption du glucose de l’intestin normal pendant l’exposition au Cr3+. Dans cette étude, nous avons étudié l’effet de l’exposition au Cr3+ dans l’absorption du glucose dans l’intestin normal.

Méthodologie: Trente rats mâle slc:ddY (26.2 ± 1.1 g) ont été aléatoirement et également assignésà trois groupes:Le groupe 1 (témoin) a reçu de l’eau potable tandis que les animaux des groupes 2 et 3 ont reçu respectivement 10 et 100 ppm de Cr3+ pendant 12 semaines par l’administration d’eau potable. Ensuite, ils ont été sacrifiés et leurs intestins excisés, rincés avec une solution de Ringer glacée (SR) et neuf sacs étirés ont été produits, avec addition de 200 µL de SR. Les sacs ont été incubés pendant 1 heure dans 5 ml de SR sans glucose et les concentrations en glucose ont été déterminées par spectrophotométrie. Le changement de potentiel trans-mural (PΔt) a été évalué à l’aide des courants de court-circuit. Les données ont été analysées par ANOVA à sens unique et p <0,05 a été considérée comme significative.

Résultats: Une diminution significative de la concentration en glucose au niveau dujéjunumdistal de la sérosa dans les groupes d’essai par rapport au témoin a été observée. La concentration en glucose des muqueuses était élevée dans la même région par rapport au témoin. Le PΔt à travers la membrane a diminué de façon significative à la fois au niveau du jéjunum distal et de l’iléon des groupes exposés au Cr3+ par rapport au témoin.

Conclusion: On peut conclure que l’exposition au Cr3+ a réduit le transport intestinal de glucose, qui pourrait probablement être un mécanisme exploré lors de la prise en charge du diabète.

Mots clés: Transport du glucose, in vitro, chrome trivalent, membrane trans-murale, souris

Correspondence: Prof. S.B. Olaleye, Department of Physiology, College of Medicine, University of Ibadan, Nigeria. E-mail: sbolaleye@yahoo.com

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Tài liệu tham khảo

Caspary WF. Absorption: General aspects and transport mechanisms in the small intestine. In:Caspary WF, ed. Structure and function of the small intestine. Amsterdam: Excerpta Medica, 1987,63-88

Zhao Y, Wieman HL, Jacobs SR, and Rathmell JC. Mechanisms and methods in glucose metabolism and cell death . Methods Enzymol. 2008; 442: 439-457.

Alada ARA and Oyebola DDO. Evidence that the gastrointestinal tract is involved in glucose homeostasis. Afr. J. Med. & Med. Sci., 1996; 25: 243-249.

Alada ARA and Oyebola DDO. The Role of Adrenergic Receptors in the increased glucose uptake by canine gut. Afr. J. Med. & Med. Sci., 1997; 26: 75-78.

Odukanmi OA, Oluwole FS and Olaleye SB. Effects of kolaviron, a Garcinia kola biflavonoid, on rat intestinal glucose absorption and alpha amylase inhibitory activities. Arch. Bas. App. Med. 2014; 2:161-167

Vinni IE, Kern F and Sussman KE. The effect of diabetes mellitus and insulin on glucose absorption by the small intestine in man. J. Lab. Clin. Med. 1965; 66:131-136.

Hediger MA. and Rhoads DB. Molecular physiology of sodium-glucose cotransporters Physiol. Rev. 1994; 74, 993–1026.

Thorens B. Glucose transporters in the regulation of intestinal, renal, and liver glucose fluxes. Am. J. Physiol.1996; 270, G541–G553.

Mueckler M. Facilitative glucose transporters. Eur J Biochem 1994. 219: 713-725.

Rajas F, Bruni N, Montano S, Zitoun C and Mithieux G: The glucose-6 phosphatase gene is expressed in human and rat small intestine: regulation of expression in fasted and diabetic rats. Gastroenterology 1999; 117:132–139

Croset M, Rajas F, Zitoun C, Hurot J, Montano S, and Mithieux G. Rat Small Intestine Is an Insulin-Sensitive Gluconeogenic Organ. Diabetes, 2001; Vol. 50: 4, 740-746

American Diabetes Association. Nutrition principles and recommendations in diabetes. Diabetes care, 2004: Vol.27, Supplement 1, S36-S46

Candilish, DJ. Trace Elements. In Proceedings of the Conference held at the Ohio Agricultural Experiment Station, Wooster, Ohio. Academic press-Inc., 2000, pp. 1-13.

Bushra FH. Status of Some Trace Elements in Iraqi Diabetic Women and its Relationship with Lipid Profile”, internal journal of science and nature. 2013, Vol. (4), No. (1), pp. 188-191

Monika K., Zimmermann MB. Low Plasm Elements in Type 2 Diabetes. Swiss Med Wkly. Inc., 2003, p.p. 133:289–292

Williams CC, Crochet BT, Bunting LD, Fernandez JM and Stanley CC. Metabolic responses of periparturient Holstein cows and heifers supplemented with chromium picolinate. Pro. Anim. Scientist, 2004; 20: 312-318

Schwarz K, Mertz W. Chromium (III) and the glucose tolerance factor. Arch Biochem Biophys. 1959; 85:292–295.

Lukaski HC. Chromium as a supplement. Ann. Rev. Nutri., 1999; 19, 279-302

Tuman RW, Doisy RJ: Metabolic effects of the glucose tolerance factor (GTF) in normal and genetically diabetic mice. Diabetes1977; 26:820–826

Nutrition Business Journal. NBJ’s Supplement Business Report. Penton Media Inc., San Diego, CA. 2003

Vincent JB. The Biochemistry of Chromium. J Nutr. 2000; 130 (4):715-718.

Cefalu WT and Hu FB. Role of chromium in human health and in diabetes. Diabetes care, 2004; Vol. 27, number 11: 2741-2751

Tasaki I, Polley EH and Orrego F. Action potentials from individual elements in cat geniculate and striate cortex. J. Neurophysiol. 1954; 17, 454-474.

Wang Z, Yang Y, Xiang X, Zhu Y, Men J, He M. Estimation of the normal range of blood glucose in rats. J of hygiene res, 2010; 39(2):133-137

Anderson RA. Chromium in the prevention and control of diabetes Diabetes Metab. 2000; 26 (1): 22-27.

Tuzcu A, Bahcecı M, Dursun M, Parmaksız Y, Ertem M, Dalgıc A, Turgut C, and Kale E. Can Long-Term Exposure to Chromium Improve Insulin Sensitivity in Chromium Mine Workers? The Journal of Trace Elements in Experimental Medicine, 2004 17:55–63

Wenk C., Gebert S., Pfirter H.P. Chromium supplements in the feed for growing pigs: influence on growth and meat quality. Arch. Anim. Nutr., 1995; 48, 71-81

Kim YJ, Sekiya F, Poulin B, Bae YS and Rhee SG. Mechanism of B-cell receptor-induced phosphorylation and activation of phospholipase C-gamma 2. Mol Cell Biol. 2004; 24 (22):9986 99

Bahijiri SM, Mira SA, Mufti AM and Ajabnoor MA: The effects of inorganic chromium and brewer’s yeast supplementation on glucose tolerance, serum lipids and drug dosage in individuals with type 2 diabetes. Saudi Med. J., 2000; 21: 831-837.

Racek J, Trefil L, Rajdl D, Mudrova V, Hunter D and Senft V: Influence of chromium-enriched yeast on blood glucose and insulin variables, blood lipids, and markers of oxidative stress in subjects with type 2 diabetes mellitus. Biol Trace Elem Res 2006; 109: 215-230.

Bösenberg LH and van Zyl DG. The mechanism of action of oral anti-diabetic drugs: A review of recent literature. JEMDSA. 2008, Vol. 13, No. 3; 80-88

Meneses JM, .Silva, MB; Sousa, M, Rosalia; SF, Pedro OG and Marco A. Antidiabetic Drugs: Mechanisms of Action and Potential Outcomes on Cellular Metabolism. JEMDSA. 2015.Vol. 21, No. 25, 2015, 3606-3620

Nelson DW, Liu X, Holst JJ, Raybould HE and Ney DM. Vagal afferents are essential for maximalresection-induced intestinal adaptive growth in orally fed rats. Am J Physiol Integr Comp Physiol 2006; 291:R1256-R1264

Baksheev L and Fuller PJ. Gene expression in the adapting small bowel after massive small bowel resection. J Gastroenterol., 2006; 41:1041-1052.

Haxhija EQ, Yang H, Spencer AU, Sun X and Teitelbaum DH. Intestinal epithelial cell proliferation is dependent on the site of massive small bowel resection. Pediatr Surg Int., 2007; 23:379-90.

Martin GR, Wallace LE and Sigalet DL. Glucagon-like peptide-2 induces intestinal adaptation in parenterally fed rats with short bowel syndrome. Am J Physiol Gastrointest Liver Physiol 2004; 286:G964-G972.

Iqbal CW, Qandeel HG, Zheng Y, Duenes JA and Sarr MG. Mechanisms of Ileal Adaptation for Glucose Absorption after Proximal-Based Small Bowel Resection. J Gastrointest Surg. 2008; 12(11): 1854-1865.

Dekaney CM, Fong JJ, Rigby RJ, Lund PK, Henning SJ and Helmrath MA. Expansion of intestinal stem cells associated with long-term adaptation following ileocecal resection in mice. Am J Physiol Gastrointest Liver Physiol. 2007; 293:G1013-G1022.

Martin GR, Wallace LE and Sigalet DL. Glucagon-like peptide-2 upregulation of intestinal blood flow and glucose uptake is nitiric oxide dependent in TPN-fed piglets. Gastroenterology. 2003; 125:136-147.