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Oxidative Medicine and Cellular Longevity
Volume 2014 (2014), Article ID 506948, 3 pages
http://dx.doi.org/10.1155/2014/506948
Editorial

Oxidative Stress and Inflammation in Obesity, Diabetes, Hypertension, and Related Cardiometabolic Complications

1Department of Physiology, University of Saskatchewan College of Medicine, 107 Wiggins Road, Saskatoon, SK, Canada S7N 5E5
2Department of Pharmacology, Center for Integrative Medicine, Center for Molecular Medicine (CIMMBA), University of Florence, Viale Pieraccini 6, 50139 Florence, Italy
3Division of Cardiology, Department of Medicine, Henry Ford Heart and Vascular Institute, 2799 West Grand Boulevard, Detroit, MI 48202-2689, USA

Received 15 January 2014; Accepted 15 January 2014; Published 27 February 2014

Copyright © 2014 Joseph Fomusi Ndisang et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


Many chronic diseases are characterized by excessive oxidative stress and inflammation [13]. The recent escalation of chronic conditions like obesity, insulin resistance, diabetes, hypertension, and other related cardiometabolic complications in all ages of the population including children, adolescences, and adults poses a great challenge to health care systems [4, 5]. Many cardiometabolic complications are multifactorial diseases and a wide variety of etiological factors including genetic, habitual, environmental, and epigenetic may be involved [4, 5]. Although these factors perturb the physiological milieu in different ways, it has been consistently shown that a common denominator amongst these factors is the production of increased oxidative stress and inflammation at various stages during the progression and development of many cardiometabolic disorders [48]. Although significant strides have been made in elucidating the role of oxidative stress and inflammation in insulin resistance, diabetes, and many cardiometabolic diseases, novel mechanistic studies are needed to broaden our knowledge on the treatment and management of these chronic conditions.

This special issue contains review papers and research articles that address a broad range of mechanistic paradigms in the pathophysiology of insulin resistance, diabetes, hypertension, obesity, and related cardiometabolic complications. The role of inflammation and apolipoproteins in the development of atherosclerotic plague, thrombosis, and related cardiac complications has been widely acknowledged [911].

Since apolipoproteins play a major pathophysiological role in atherosclerosis, in an article featuring in this special issue, A. J. Lepedda et al. used two-dimensional electrophoresis (2DE) coupled with Matrix-Assisted Laser Desorption/Ionization (MALDI), Time of Flight (TOF), and Mass Spectrometry (MS) analysis to characterize the apolipoprotein components of very-low-density lipoprotein (VLDL), low-density lipoprotein (LDL), and high-density lipoprotein (HDL) from plasma of patients undergoing carotid endarterectomy. The study of A. J. Lepedda et al. will unveil novel perspectives on the pathophysiological role of apolipoproteins in development of atherosclerotic plague. In another related article featuring in this special issue, W. Sun et al. showed that a herbal extract obtained from the medicinal plant Magnolia officinalis attenuated cardiac hypertrophy and cardiac dysfunction by reducing myocardial lipid accumulation, inflammation, oxidative stress, and apoptosis in animals fed with high-fat diet. Interestingly, the benefit of Magnolia officinalis is not limited to myocardial dysfunction. In another study by W. Cui et al. reported in this special issue, Magnolia officinalis was shown to abate several markers of inflammation and oxidative stress in the kidneys including tumor necrosis factor-α, plasminogen activator inhibitor-1, 3-nitrotyrosine, and 4-hydroxy-2-nonenal. Interestingly, the suppression of these prooxidative/inflammatory agents were associated with the potentiation of peroxisome proliferator-activated receptor-γ coactivator-1α and hexokinase II, with improved renal morphology and the reduction of proteinuria suggesting improved renal function.

An important cytoprotective enzyme with benefits against diabetes, hypertension, obesity, and related cardiometabolic complications is heme oxygenase [13, 1215]. In a related article featuring in this special issue, S. Tiwari et al. showed that the heme oxygenase system improves cardiac function by attenuating markers of heart failure, cardiac hypertrophy/lesions, extracellular matrix/profibrotic proteins, and inflammatory/oxidative mediators, while concomitantly enhancing adiponectin and atrial natriuretic peptide in obese rats with insulin resistance. Similarly, Y. Son et al. wrote a review article that delineates the protective mechanisms of heme oxygenase in metabolic diseases. Furthermore, Md. J. Uddin and coworkers demonstrated in a research article that carbon monoxide, a product generated by heme oxygenase, suppressed inflammation in colitis mice model via inhibition of glycogen synthase kinase-3, a serine-threonine protein kinase implicated in glycogen metabolism, and other cellular functions including apoptosis [16, 17]. Besides the heme oxygenase system, other molecules including trace elements are important in the regulation of cardiometabolic functions [18, 19]. Emerging evidence indicates that perturbations in the delicate balance of trace elements such as copper and zinc may offset redox equilibrium in physiological milieu leading to oxidative stress and eventually to the development of diabetes and diabetic complications [2022]. In this special issue, J. Xu et al. reported novel insights on zinc/copper ratio in patients with different pathological profiles including impaired fasting glucose, impaired glucose tolerance type-1 diabetes, and type-2 diabetes.

Collectively, the articles presented in this special issue would unveil novel concepts that would stimulate further research in this area of considerable interest given the escalation of diabetes, obesity, hypertension, and related cardiometabolic complications in all ages of the population including children.

Joseph Fomusi Ndisang
Alfredo Vannacci
Sharad Rastogi

References

  1. A. Jadhav and J. F. Ndisang, “Heme arginate suppresses cardiac lesions and hypertrophy in deoxycorticosterone acetate-salt hypertension,” Experimental Biology and Medicine, vol. 234, no. 7, pp. 764–778, 2009. View at Publisher · View at Google Scholar · View at Scopus
  2. J. F. Ndisang and A. Jadhav, “Upregulating the heme oxygenase system suppresses left ventricular hypertrophy in adult spontaneously hypertensive rats for 3 months,” Journal of Cardiac Failure, vol. 15, no. 7, pp. 616–628, 2009. View at Publisher · View at Google Scholar · View at Scopus
  3. J. F. Ndisang, A. Jadhav, and J. Fomusi Ndisang, “The heme oxygenase system attenuates pancreatic lesions and improves insulin sensitivity and glucose metabolism in deoxycorticosterone acetate hypertension,” The American Journal of Physiology—Regulatory Integrative and Comparative Physiology, vol. 298, no. 1, pp. R211–R223, 2010. View at Publisher · View at Google Scholar · View at Scopus
  4. V. S. Malik, W. C. Willett, and F. B. Hu, “Global obesity: trends, risk factors and policy implications,” Nature Reviews Endocrinology, vol. 9, pp. 13–27, 2013. View at Google Scholar
  5. J. C. Han, D. A. Lawlor, and S. Y. Kimm, “Childhood obesity,” The Lancet, vol. 375, no. 9727, pp. 1737–1748, 2010. View at Publisher · View at Google Scholar · View at Scopus
  6. Y. Hirata, M. Tabata, H. Kurobe et al., “Coronary atherosclerosis is associated with macrophage polarization in epicardial adipose tissue,” Journal of the American College of Cardiology, vol. 58, no. 3, pp. 248–255, 2011. View at Publisher · View at Google Scholar · View at Scopus
  7. J. F. Navarro-González, C. Mora-Fernández, M. M. De Fuentes, and J. García-Pérez, “Inflammatory molecules and pathways in the pathogenesis of diabetic nephropathy,” Nature Reviews Nephrology, vol. 7, no. 6, pp. 327–340, 2011. View at Publisher · View at Google Scholar · View at Scopus
  8. J. F. Navarro-Gonzalez and C. Mora-Fernandez, “Inflammatory pathways,” Contributions to Nephrology, vol. 170, pp. 113–123, 2011. View at Publisher · View at Google Scholar
  9. E. Lutgens, R.-J. Van Suylen, B. C. Faber et al., “Atherosclerotic plaque rupture: local or systemic process?” Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 23, no. 12, pp. 2123–2130, 2003. View at Publisher · View at Google Scholar · View at Scopus
  10. P. Libby, “Inflammation in atherosclerosis,” Nature, vol. 420, no. 6917, pp. 868–874, 2002. View at Publisher · View at Google Scholar · View at Scopus
  11. K. Skålén, M. Gustafsson, E. Knutsen Rydberg et al., “Subendothelial retention of atherogenic lipoproteins in early atherosclerosis,” Nature, vol. 417, no. 6890, pp. 750–754, 2002. View at Publisher · View at Google Scholar · View at Scopus
  12. A. Jadhav, E. Torlakovic, and J. F. Ndisang, “Hemin therapy attenuates kidney injury in deoxycorticosterone acetate-salt hypertensive rats,” The American Journal of Physiology—Renal Physiology, vol. 296, no. 3, pp. F521–F534, 2009. View at Publisher · View at Google Scholar · View at Scopus
  13. J. F. Ndisang, N. Lane, and A. Jadhav, “Upregulation of the heme oxygenase system ameliorates postprandial and fasting hyperglycemia in type 2 diabetes,” The American Journal of Physiology—Endocrinology and Metabolism, vol. 296, no. 5, pp. E1029–E1041, 2009. View at Publisher · View at Google Scholar · View at Scopus
  14. J. F. Ndisang and A. Jadhav, “Hemin therapy improves kidney function in male streptozotocin-induced diabetic rats: role of the heme oxygenase/atrial natriuretic peptide/adiponectin axis,” Endocrinology, vol. 155, pp. 215–229, 2014. View at Publisher · View at Google Scholar
  15. J. F. Ndisang and A. Jadhav, “Hemin therapy suppresses inflammation and retroperitoneal adipocyte hypertrophy to improve glucose metabolism in obese rats co-morbid with insulin-resistant type-2 diabetes,” Diabetes, Obesity and Metabolism, vol. 15, pp. 1029–1039, 2013. View at Publisher · View at Google Scholar
  16. X. Tang, D. Zheng, P. Hu et al., “Glycogen synthase kinase 3 beta inhibits microRNA-183-96-182 cluster via the beta-Catenin/TCF/LEF-1 pathway in gastric cancer cells,” Nucleic Acids Research, 2013. View at Publisher · View at Google Scholar
  17. A. Ali, K. P. Hoeflich, and J. R. Woodgett, “Glycogen synthase kinase-3: properties, functions, and regulation,” Chemical Reviews, vol. 101, no. 8, pp. 2527–2540, 2001. View at Publisher · View at Google Scholar · View at Scopus
  18. H. E. Poulsen, E. Specht, K. Broedbaek et al., “RNA modifications by oxidation: a novel disease mechanism?” Free Radical Biology and Medicine, vol. 52, no. 8, pp. 1353–1361, 2012. View at Publisher · View at Google Scholar · View at Scopus
  19. G. J. Cooper, “Selective divalent copper chelation for the treatment of diabetes mellitus,” Current Medicinal Chemistry, vol. 19, pp. 2828–2860, 2012. View at Publisher · View at Google Scholar
  20. B. Li, Y. Tan, W. Sun, Y. Fu, L. Miao, and L. Cai, “The role of zinc in the prevention of diabetic cardiomyopathy and nephropathy,” Toxicology Mechanisms and Methods, vol. 23, pp. 27–33, 2013. View at Publisher · View at Google Scholar
  21. L. Sun, Y. Yu, T. Huang et al., “Associations between ionomic profile and metabolic abnormalities in human population,” PLoS ONE, vol. 7, Article ID e38845, 2012. View at Google Scholar
  22. Y. Zheng, X.-K. Li, Y. Wang, and L. Cai, “The role of zinc, copper and iron in the pathogenesis of diabetes and diabetic complications: therapeutic effects by chelators,” Hemoglobin, vol. 32, no. 1-2, pp. 135–145, 2008. View at Publisher · View at Google Scholar · View at Scopus