Glucosamine modulates membrane and cellular ionic homeostasis: studies on accelerated senescent and naturally aged rats

References

• Hartl FU. Cellular homeostasis and aging. Annu Rev Biochem. 2016;85(1):1–4.
   PubMed Web of Science ®Google Scholar
• Pomatto LCD, Davies KJA. The role of declining adaptive homeostasis in ageing. J Physiol. 2017;595(24):7275–7309.
   PubMed Web of Science ®Google Scholar
• Pandey KB, Rizvi SI. Resveratrol up-Regulates the erythrocyte plasma membrane redox system and mitigates oxidation-Induced alterations in erythrocytes during aging in humans. Rejuvenation Res. 2013;16(3):232–240.
   Web of Science ®Google Scholar
• Pandey KB, Rizvi SI. Markers of oxidative stress in erythrocytes and plasma during aging in humans. Oxid Med Cell Longev. 2010;3(1):2–12.
   PubMed Web of Science ®Google Scholar
• Andrews NW, Corrotte M. Plasma membrane repair. Curr Biol. 2018;28(8):R392–R397.
   PubMed Web of Science ®Google Scholar
• Bartosz G. Erythrocyte aging: physical and chemical membrane changes. Gerontology. 1991;37(1–3):33–67.
   PubMed Web of Science ®Google Scholar
• Kaestner L, Minetti G. The potential of erythrocytes as cellular aging models. Cell Death Differ. 2017;24(9):1475–1477.
   Web of Science ®Google Scholar
• Singh AK, Singh S, Garg G, et al. Rapamycin mitigates erythrocyte membrane transport functions and oxidative stress during aging in rats. Arch Physiol Biochem. 2018a;124(1):45–53.
   PubMed Web of Science ®Google Scholar
• Pandey KB, Rizvi SI. Role of resveratrol in regulation of membrane transporters and integrity of human erythrocytes. Biochem Biophys Res Commun. 2014a;453(3):521–526.
   PubMed Web of Science ®Google Scholar
• Bissett DL. Glucosamine: an ingredient with skin and other benefits. J Cosmet Dermatol. 2006;5(4):309–315.
   Google Scholar
• Ingram DK, Roth GS. Glycolytic inhibition: an effective strategy for developing calorie restriction mimetics. GeroScience. 2020; Preprint. doi:10.1007/s11357-020-00298-7
   Web of Science ®Google Scholar
• Ingram DK, Roth GS. Glycolytic inhibition: an effective strategy for developing calorie restriction mimetics. GeroScience. 2021;43(3):1159–1169.
   Web of Science ®Google Scholar
• Anderson JW, Nicolosi RJ, Borzelleca JF. Glucosamine effects in humans: a review of effects on glucose metabolism, side effects, safety considerations and efficacy. Food Chem Toxicol. 2005;43(2):187–201.
   PubMed Web of Science ®Google Scholar
• Ingram DK, Roth GS. Calorie restriction mimetics: can you have your cake and eat it, too? Ageing Res Rev. 2015;20:46–62.
   PubMed Web of Science ®Google Scholar
• Kumar R, Saraswat K, Rizvi SI. Glucosamine displays a potent caloric restriction mimetic effect in senescent rats by activating mitohormosis. Rejuvenation Res. 2021;24(3):220–226.
   Web of Science ®Google Scholar
• Azman KF, Zakaria R. d-Galactose-induced accelerated aging model: an overview. Biogerontology. 2019;20(6):763–782.
   PubMed Web of Science ®Google Scholar
• Song X, Bao M, Li D, et al. Advanced glycation in d-galactose induced mouse aging model. Mech Ageing Dev. 1999;108(3):239–251.
   PubMed Web of Science ®Google Scholar
• Kumar R, Kumar M, Rizvi SI. Chitosan displays a potent caloric restriction mimetic effect in senescent rats. Rejuvenation Res. 2021;24(5):390–396.
   Web of Science ®Google Scholar
• Tripathi SS, Kumar R, Bissoyi A, et al. Baicalein may act as a caloric restriction mimetic candidate to improve the antioxidant profile in a natural rodent model of aging. Rejuvenation Res. 2022;25(2):70–78.
   Web of Science ®Google Scholar
• Marchesi VT, Palade GE. THE LOCALIZATION OF Mg-Na-K-ACTIVATED ADENOSINE TRIPHOSPHATASE ON RED CELL GHOST MEMBRANES. J Cell Biol. 1967;35(2):385–404.
   PubMed Web of Science ®Google Scholar
• Suhail M. Na+, K+-ATPase: ubiquitous multifunctional transmembrane protein and its relevance to various pathophysiological conditions. J Clin Med Res. 2010; Preprint. doi:10.4021/jocmr2010.02.263w
   Google Scholar
• Matteucci E. ERYTHROCYTE SODIUM/HYDROGEN EXCHANGE INHIBITION BY (−) EPICATECHIN. Cell Biol Int. 2001a;25(8):771–776.
   PubMed Web of Science ®Google Scholar
• Levine RL, et al. Determination of carbonyl content in oxidatively modified proteins. In Methods in Enzymology 186 Elsevier; 1990. p 464–478. DOI: 10.1016/0076-6879(90)86141-H
   Google Scholar
• Spyridaki M-HE, Siskos PA. An improved spectrophotometric method for the determination of free, bound and total N-acetylneuraminic acid in biological fluids. Anal Chim Acta. 1996;327(3):277–285.
   Web of Science ®Google Scholar
• Firuzi O, Mladěnka P, Riccieri V, et al. Parameters of oxidative stress status in healthy subjects: their correlations and stability after sample collection. J Clin Lab Anal. 2006;20(4):139–148.
   PubMed Web of Science ®Google Scholar
• Kitajima H, Yamaguchi T, Kimoto E. Hemolysis of human erythrocytes under hydrostatic pressure is suppressed by cross-linking of membrane proteins. J Biochem. 1990;108(6):1057–1062.
   PubMed Web of Science ®Google Scholar
• Rao V, Kaja S, and Gentile S. Ion channels in aging and aging-related diseases. In Shiomi N, editor. Molecular mechanisms of the aging process and rejuvenation. Kobe college, Japan: InTech; 2016. doi:10.5772/63951
   Google Scholar
• Weimer S, Priebs J, Kuhlow D, et al. D-Glucosamine supplementation extends life span of nematodes and of ageing mice. Nat Commun. 2014;5(1):3563.
   PubMedGoogle Scholar
• Lv C, Wang L, Zhu X, et al. Glucosamine promotes osteoblast proliferation by modulating autophagy via the mammalian target of rapamycin pathway. Biomed Pharmacothe. 2018;99:271–277.
   Web of Science ®Google Scholar
• Shintani T, Kosuge Y, Ashida H. Glucosamine extends the lifespan of caenorhabditis elegans via autophagy induction. J. Appl. Glycosci. 2018;65(3):37–43.
   Web of Science ®Google Scholar
• Bogdanova A, Makhro A, Wang J, et al. Calcium in red blood cells—A perilous balance. Int J Mol Sci. 2013;14(5):9848–9872.
   Web of Science ®Google Scholar
• Kim J, Lee H, Shin S. Advances in the measurement of red blood cell deformability: a brief review. J Cell Biotechnol. 2015;1(1):63–79.
   Google Scholar
• Viskupicova J, Blaskovic D, Galiniak S, et al. Effect of high glucose concentrations on human erythrocytes in vitro. Redox Biol. 2015;5:381–387.
   PubMed Web of Science ®Google Scholar
• Stafford N, Wilson C, Oceandy D, et al. ‘The plasma membrane calcium ATP ases and their role as major new players in human disease’. Physiol Rev. 2017;97(3):1089–1125.
   PubMed Web of Science ®Google Scholar
• Zaidi A. Plasma membrane Ca 2+ -ATPases: targets of oxidative stress in brain aging and neurodegeneration. World J Biol Chem. 2010;1(9):271.
   PubMedGoogle Scholar
• Clausen MV, Hilbers F, Poulsen H. The structure and function of the Na,K-ATPase isoforms in health and disease. Front Physiol. 2017;8:371.
   PubMed Web of Science ®Google Scholar
• Rossi L, Fraternale A, Bianchi M, et al. Red blood cell membrane processing for biomedical applications. Front Physiol. 2019;10:1070.
   PubMed Web of Science ®Google Scholar
• Namazi G, Asa P, Sarrafzadegan N, et al. Decreased Na+/K+-ATPase activity and altered susceptibility to peroxidation and lipid composition in the erythrocytes of metabolic syndrome patients with coronary artery disease. Ann Nutr Metab. 2019;74(2):140–148.
   Web of Science ®Google Scholar
• Jamialahmadi K, Arasteh O, Matbou Riahi M, et al. Protective effects of glucosamine hydrochloride against free radical-induced erythrocytes damage. Environ Toxicol Pharmacol. 2014;38(1):212–219.
   Web of Science ®Google Scholar
• Bobulescu IA, Di Sole F, Moe OW. Na+/H+ exchangers: physiology and link to hypertension and organ ischemia. Curr Opin Nephrol Hypertens. 2005;14(5):485–494.
   PubMed Web of Science ®Google Scholar
• Aoi W, Marunaka Y. Importance of pH homeostasis in metabolic health and diseases: crucial role of membrane proton transport. Biomed Res Int. 2014;2014:1–8.
   Web of Science ®Google Scholar
• Sun Y-M, Su Y, Li J, et al. Role of the Na+/H+ exchanger on the development of diabetes mellitus and its chronic complications. Biochem Biophys Res Commun. 2012;427(2):229–231.
   Web of Science ®Google Scholar
• Kalogeris T, et al. Cell biology of ischemia/reperfusion injury. In: International review of cell and molecular biology. Elsevier; 2012. p 229–317. DOI: 10.1016/B978-0-12-394309-5.00006-7
   Google Scholar
• Dalirfardouei R, Karimi G, Jamialahmadi K. Molecular mechanisms and biomedical applications of glucosamine as a potential multifunctional therapeutic agent. Life Sci. 2016;152:21–29.
   PubMed Web of Science ®Google Scholar
• Fang C, Peng M, Li G, et al. New functions of glucosamine as a scavenger of the lipid peroxidation product malondialdehyde. Chem Res Toxicol. 2007;20(6):947–953.
   Web of Science ®Google Scholar
• Balcerczyk A, Bartosz G. Thiols are main determinants of total antioxidant capacity of cellular Homogenates. Free Radic Res. 2003;37(5):537–541.
   PubMed Web of Science ®Google Scholar
• Zhu Y, Carvey PM, Ling Z. Age-related changes in glutathione and glutathione-related enzymes in rat brain. Brain Res. 2006;1090(1):35–44.
   Google Scholar
• Kapoor M, Mineau F, Fahmi H, et al. ‘Glucosamine sulfate reduces prostaglandin E2Production in osteoarthritic chondrocytes through inhibition of microsomal PGE synthase-1’. J Rheumatol. 2012;39(3):635–644.
   Web of Science ®Google Scholar
• Mazzanti L, Rabini RA, Salvolini E, et al. Sialic acid, diabetes, and aging: a study on the erythrocyte membrane. Metabolism. 1997;46(1):59–61.
   Web of Science ®Google Scholar
• Kumar D, Rizvi SI. Erythrocyte membrane bound and plasma sialic acid during aging. Biologia. 2013;68(4):762–765.
   Web of Science ®Google Scholar
• Gordon MB, Kloxin CJ, Wagner NJ. Structural and rheological aging in model attraction-driven glasses by Rheo-SANS. Soft Matter. 2021;17(4):924–935.
   Web of Science ®Google Scholar