Galangin controls streptozotocin-caused glucose homeostasis and reverses glycolytic and gluconeogenic enzyme changes in rats

References

• Alberti, K.G.M.M., and Press, C.M., 1982. The biochemistry and complications of diabetes. In: H. Keen and J. Javve, eds. Complications of diabetes. London: Edward Arnold Publishers, 231–270.
   Google Scholar
• Aloud, A.A., et al., 2017. Galangin, a dietary flavonoid, improves antioxidant status and reduces hyperglycemia-mediated oxidative stress in streptozotocin-induced diabetic rats. Redox Report: Communications in Free Radical Research, 22 (6), 290–300.
   PubMed Web of Science ®Google Scholar
• Aloud, A.A., et al., 2018. Galangin, a natural flavonoid reduces mitochondrial oxidative damage in streptozotocin-induced diabetic rats. Redox Report: Communications in Free Radical Research, 23 (1), 29–34.
   PubMed Web of Science ®Google Scholar
• Alqurashi, K.A., et al., 2011. Prevalence of diabetes mellitus in a Saudi community. Annals of Saudi Medicine, 31 (1), 19–23.
   PubMed Web of Science ®Google Scholar
• Ankita, P., et al., 2015. Flavonoid rich fraction of Punica granatum improves early diabetic nephropathy by ameliorating proteinuria and disturbed glucose homeostasis in experimental animals. Pharmaceutical Biology, 53 (1), 61–71.
   PubMed Web of Science ®Google Scholar
• Baquer, N.Z., et al., 1998. Regulations of metabolic pathways in liver and kidney during experimental diabetes. Effect of antidiabetic compounds. Indian Journal of Clinical Biochemistry, 13 (2), 63–80.
   PubMedGoogle Scholar
• Bestwick, C.S., and Milne, L., 2006. Influence of galangin on HL-60 cell proliferation and survival. Cancer Letters, 243 (1), 80–89.
   PubMed Web of Science ®Google Scholar
• Brandstrup, N., Kirk, J.E., and Bruni, C., 1957. The hexokinase and phosphoglucoisomerase activities of aortic and pulmonary artery tissue in individuals of various ages. Journal of Gerontology, 12 (2), 166–171.
   PubMedGoogle Scholar
• Burchell, A., Allan, B.B., and Hume, R., 1994. Glucose-6-phosphatase proteins of the endoplasmic reticulum. Molecular Membrane Biology, 11 (4), 217–227.
   PubMed Web of Science ®Google Scholar
• Calisti, L., and Tognetti, S., 2005. Measure of glycosylated hemoglobin. Acta Biomedica, 76 (3), 59–62.
   PubMedGoogle Scholar
• Chatterjee, M.N., and Shinde, R., 2000. Textbook of medical biochemistry. Metabolism of carbohydrates. Delhi: JayPee Medical Publishers, 421.
   Google Scholar
• Cordero-Herrera, I., et al., 2013. Cocoa flavonoids improve insulin signalling and modulate glucose production via AKT and AMPK in HepG2 cells. Molecular Nutrition & Food Research, 57 (6), 974–985.
   PubMed Web of Science ®Google Scholar
• Coskun, O., et al., 2005. Quercetin, a flavonoid antioxidant, prevents and protects streptozotocin-induced oxidative stress and beta-cell damage in rat pancreas. Pharmacological Research, 51 (2), 117–123.
   PubMed Web of Science ®Google Scholar
• Drabkin, D.L., and Austin, J.M., 1932. Spectrophotometric constants for common haemoglobin derivatives in human, dog and rabbit blood. The Journal of Biological Chemistry, 98, 719–733.
   Google Scholar
• Ells, H.A., and Kirkman, H.N., 1961. A colorimetric method for assay of erythrocytic glucose6-phosphate dehydrogenase. Proceedings of the Society for Experimental Biology and Medicine, 106 (3), 607–609.
   PubMed Web of Science ®Google Scholar
• Fröde, T.S., and Medeiros, Y.S., 2008. Animal models to test drugs with potential antidiabetic activity. Journal of Ethnopharmacology, 115 (2), 173–183.
   PubMed Web of Science ®Google Scholar
• Gancedo, J.M., and Gancedo, C., 1971. Fructose-1,6diphosphatase, phosphofructokinase and glucose-6-phosphate dehydrogenase from fermenting and non fermenting yeasts. Archives of Microbiology, 76 (2), 132–138.
   Google Scholar
• Heo, M.Y., et al., 2001. Anti-genotoxicity of galangin as a cancer chemopreventive agent candidate. Mutation Research, 488 (2), 135–150.
   PubMed Web of Science ®Google Scholar
• Jung, Y.C., et al., 2014. Anti-inflammatory effects of galangin on lipopolysaccharide-activated macrophages via ERK and NF-κB pathway regulation. Immunopharmacology and Immunotoxicology, 36 (6), 426–432.
   PubMed Web of Science ®Google Scholar
• Kalaiarasi, P., and Pugalendi, K.V., 2009. Antihyperglycemic effect of 18 beta-glycyrrhetinic acid, aglycone of glycyrrhizin, on streptozotocin-diabetic rats. European Journal of Pharmacology, 606 (1–3), 269–273.
   PubMed Web of Science ®Google Scholar
• Kasetti, R.B., et al., 2010. Antihyperglycemic and antihyperlipidemic activities of methanol:water (4:1) fraction isolated from aqueous extract of Syzygium alternifolium seeds in streptozotocin induced diabetic rats. Food Chemical Toxicology, 48 (4), 1078–1084.
   PubMed Web of Science ®Google Scholar
• Koide, H., and Oda, T., 1959. Pathological occurrence of glucose-6-phosphatase in serum in liver diseases. Clinica Chimica Acta: International Journal of Clinical Chemistry, 4, 554–561.
   PubMed Web of Science ®Google Scholar
• Kondeti, V.K., et al., 2010. Effect of Pterocarpus santalinus bark, on blood glucose, serum lipids, plasma insulin and hepatic carbohydrate metabolic enzymes in streptozotocin-induced diabetic rats. Food Chemical and Toxicoogyl, 48 (5), 1281–1287.
   PubMed Web of Science ®Google Scholar
• Kumar, S., and Alagawadi, K.R., 2013. Anti-obesity effects of galangin, a pancreatic lipase inhibitor in cafeteria diet fed female rats. Pharmaceutical Biology, 51 (5), 607–613.
   PubMed Web of Science ®Google Scholar
• Li, F., et al., 2010. Study on the constituents of Mexican propolis and their cytotoxic activity against PANC-1 human pancreatic cancer cells. Journal of Natural Products, 73 (4), 623–627.
   PubMed Web of Science ®Google Scholar
• Meyer, J.J.M., et al., 1997. Antiviral activity of galangin isolated from the aerial parts of Helichrysum aureonitens. Journal of Ethnopharmacology, 56 (2), 165–169.
   PubMed Web of Science ®Google Scholar
• Morales, M.A., et al., 1973. Mutations affecting accumulation of glycogen. Neurospora News, 20 (1), 24–25.
   Google Scholar
• Murray, R. K., et al., 2000., Harper’s biochemistry, 25th edn. Stanford: Appleton and Lange, 610–617.
   Google Scholar
• Nayak, S.S., and Pattabiraman, T.N., 1981. A new colorimetric method for the estimation of glycosylated hemoglobin. Clinica Chimica Acta: International Journal of Clinical Chemistry, 109 (3), 267–274.
   PubMed Web of Science ®Google Scholar
• Nordlie, R.C., et al., 1999. Lange, A.J., Regulation of glucose production by the liver. Annual Review of Nutrition, 19, 379–406.
   PubMed Web of Science ®Google Scholar
• Ohno, M., et al., 2013. The flavonoid apigenin improves glucose tolerance through inhibition of microRNA maturation in miRNA103 transgenic mice. Scientific Reports, 3 (1), 25–53.
   Google Scholar
• Porksen, N.K., et al., 1996. Mechanisms of sulfonylurea's stimulation of insulin secretion in vivo: selective amplification of insulin secretory burst mass. Diabetes, 45 (12), 1792–1797.
   PubMed Web of Science ®Google Scholar
• Scheen, A.J., 1997. Drug treatment of non-insulin-dependent diabetes mellitus in 1990s. Achievements and future developments. Drugs, 54 (3), 355–368.
   PubMed Web of Science ®Google Scholar
• Sivakumar, A.S., and Anuradha, C.V., 2011. Effect of galangin supplementation on oxidative damage and inflammatory changes in fructose-fed rat liver. Chemico-Biological Interactions, 193 (2), 141–148.
   PubMed Web of Science ®Google Scholar
• Sivakumar, A.S., et al., 2010. Dose-dependent effect of galangin on fructose-mediated insulin resistance and oxidative events in rat kidney. Redox Report, 15 (5), 224–232.
   PubMed Web of Science ®Google Scholar
• Swanston-Flatt, S.K., et al., 1990. Traditional plant treatments for diabetes. Studies in normal and streptozotocin diabetic mice. Diabetologia, 33 (8), 462–464.
   PubMed Web of Science ®Google Scholar
• Szkudelski, T., 2001. The mechanism of alloxan and streptozotocin action in B cells of the rat pancreas. Physiological Research, 50 (6), 537–546.
   PubMed Web of Science ®Google Scholar
• Tamiru, W., et al., 2012. Evaluation of the effects of 80% methanolic leaf extract of Caylusea abyssinica (fresen.) fisch. & Mey. on glucose handling in normal, glucose loaded and diabetic rodents. BMC Complementary and Alternative Medicine, 12 (1), 151.
   PubMedGoogle Scholar
• Trinder, P., 1969. Determination of blood glucose using an oxidase peroxidase system with a non-carcinogenic chromogen. Annals of Clinical Biochemistry, 6, 24–30.
   Google Scholar
• West, I.C., 2002. Glucose-6-phosphate dehydrogenase: a candidate gene for diabetes. Diabetic Medicine, 19 (2), 172–174.
   PubMed Web of Science ®Google Scholar
• Wilding, J., 2006. Thiazolidinediones, insulin resistance and obesity: finding a balance. International Journal of Clinical Practice, 60 (10), 1272–1280.
   PubMed Web of Science ®Google Scholar
• Xu, Y., et al., 2005. Diabetes causes inhibition of glucose- 6 phosphate dehydrogenase via activation of PKA, which contributes to oxidative stress in rat kidney cortex. American Journal of Physiology Renal Physiology, 289 (5), F1040–F1047.
   PubMed Web of Science ®Google Scholar
• Yang, M., et al., 2014. Study on hypoglycemic effect and mechanism of total flavonoids of Propolis in STZ diabetic rats. Zhong Yao Cai, 37 (9), 1623–1626.
   PubMedGoogle Scholar
• Zielonka, J., et al., 2003. Radical scavenging properties of genistein. Free Radical Biology & Medicine, 35 (8), 958–965.
   PubMed Web of Science ®Google Scholar