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Editorial Molecular Basis of the Inflammation Related to Obesity Ana B. Crujeiras , 1,2 Paul Cordero , 3 Diego F. Garcia-Diaz , 4 Ewa Stachowska , 5 and Pedro González-Muniesa 2,6,7,8 1 Epigenomics in Endocrinology and Nutrition Group, Epigenomics Unit, Instituto de Investigacion Sanitaria de Santiago (IDIS), Complejo Hospitalario Universitario de Santiago (CHUS/SERGAS), Santiago de Compostela, Spain 2 CIBERobn Physiopathology of Obesity and Nutrition, Centre of Biomedical Research Network, ISCIII, Madrid, Spain 3 Institute for Liver and Digestive Health, University College London, Royal Free Hospital, Rowland Hill Street, London, UK 4 Laboratorio de Nutrigenomica, Departamento de Nutricion, Facultad de Medicina, Universidad de Chile, Chile 5 Department of Biochemistry and Human Nutrition, Pomeranian Medical University, Szczecin, Poland 6 University of Navarra, Department of Nutrition, Food Science and Physiology, School of Pharmacy and Nutrition, Pamplona, Spain 7 University of Navarra, Centre for Nutrition Research, School of Pharmacy and Nutrition, Pamplona, Spain 8 IDISNA, Navarras Health Research Institute, Pamplona, Spain Correspondence should be addressed to Pedro González-Muniesa; [email protected] Received 30 January 2019; Accepted 30 January 2019; Published 17 February 2019 Copyright © 2019 Ana B. Crujeiras 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. Almost two thousand millions of adults suer from over- weight or obesity in the world [1]. After decades of research, we understand that the solution to this problem is not easy, as the pernicious trend is still increasing [2]. This disease is dened as an excessive fat accumulation together with a moderate but chronic inammation [3]. This accompanying proinammatory status is considered the link between obesity and the development of its related comorbidities such as insulin resistance and type 2 diabetes, cardiovascular diseases, cancer, and nonalcoholic fatty liver disease [4]. The main triggers for this inammation have been tra- ditionally considered oxygen tension, oxidative stress, and endoplasmic reticulum stress [5]. This special issue con- tains articles analyzing oxidative stress, adipokine secretory pattern, methylation, or nanomedicine to further untangle the processes involved in this disease and to oer promi- sing/possible alternative therapeutical tools. In this sense, D. Stygar and collaborators measured in rats the levels of selected adipokines and other proteins, such as FABP4, leptin, chemerin, and CRP, to show the proinam- matory eect of a high-fat diet. Interestingly, this eect was reversed by the treatment of obesity with metabolic surgery. As mentioned earlier, it seems clear the relation of an abnor- mally enlarged adipose tissue and oxidative stress as it has been analyzed in the article of Y. Gramlich and coworkers. These authors suggest that obese patients undergoing coro- nary artery bypass grafting showed altered myocardial redox patterns, indicating an increased oxidative stress with inade- quate antioxidant compensation. This might explain why patients with high BMI suering from coronary artery dis- ease are more susceptible to cardiomyopathy and possible damage by ischemia and reperfusion, for example, during cardiac surgery. On the other hand, oxidative stress seems to be related with diabetic retinopathy, one of the multiple accompanying side-eects of obesity [6]. In this sense, A. Maugeri and collaborators stated that hyperglycemia increased ROS production and alters the DNA methylation process, therefore altering the expression of certain genes. They also found in their study that curcumin seems to reduce oxidative stress and improves methylation activities, consid- ering this compound an eective antioxidant to counteract this condition. In the same area, another potent antioxidant with self-regenerative properties, nanoparticles of cerium oxide, was tested by A. Lopez-Pascual and coworkers in three types of cells (adipocytes, macrophages, and myotubes) under Hindawi Oxidative Medicine and Cellular Longevity Volume 2019, Article ID 5250816, 2 pages https://doi.org/10.1155/2019/5250816

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Page 1: Editorial Molecular Basis of the Inflammation …downloads.hindawi.com/journals/omcl/2019/5250816.pdfEditorial Molecular Basis of the Inflammation Related to Obesity Ana B. Crujeiras

EditorialMolecular Basis of the Inflammation Related to Obesity

Ana B. Crujeiras ,1,2 Paul Cordero ,3 Diego F. Garcia-Diaz ,4 Ewa Stachowska ,5

and Pedro González-Muniesa 2,6,7,8

1Epigenomics in Endocrinology and Nutrition Group, Epigenomics Unit, Instituto de Investigacion Sanitaria de Santiago (IDIS),Complejo Hospitalario Universitario de Santiago (CHUS/SERGAS), Santiago de Compostela, Spain2CIBERobn Physiopathology of Obesity and Nutrition, Centre of Biomedical Research Network, ISCIII, Madrid, Spain3Institute for Liver and Digestive Health, University College London, Royal Free Hospital, Rowland Hill Street, London, UK4Laboratorio de Nutrigenomica, Departamento de Nutricion, Facultad de Medicina, Universidad de Chile, Chile5Department of Biochemistry and Human Nutrition, Pomeranian Medical University, Szczecin, Poland6University of Navarra, Department of Nutrition, Food Science and Physiology, School of Pharmacy and Nutrition, Pamplona, Spain7University of Navarra, Centre for Nutrition Research, School of Pharmacy and Nutrition, Pamplona, Spain8IDISNA, Navarra’s Health Research Institute, Pamplona, Spain

Correspondence should be addressed to Pedro González-Muniesa; [email protected]

Received 30 January 2019; Accepted 30 January 2019; Published 17 February 2019

Copyright © 2019 Ana B. Crujeiras et al. This is an open access article distributed under the Creative Commons AttributionLicense, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work isproperly cited.

Almost two thousand millions of adults suffer from over-weight or obesity in the world [1]. After decades of research,we understand that the solution to this problem is not easy, asthe pernicious trend is still increasing [2].

This disease is defined as an excessive fat accumulationtogether with a moderate but chronic inflammation [3].This accompanying proinflammatory status is consideredthe link between obesity and the development of its relatedcomorbidities such as insulin resistance and type 2 diabetes,cardiovascular diseases, cancer, and nonalcoholic fatty liverdisease [4].

The main triggers for this inflammation have been tra-ditionally considered oxygen tension, oxidative stress, andendoplasmic reticulum stress [5]. This special issue con-tains articles analyzing oxidative stress, adipokine secretorypattern, methylation, or nanomedicine to further untanglethe processes involved in this disease and to offer promi-sing/possible alternative therapeutical tools.

In this sense, D. Stygar and collaborators measured inrats the levels of selected adipokines and other proteins, suchas FABP4, leptin, chemerin, and CRP, to show the proinflam-matory effect of a high-fat diet. Interestingly, this effect wasreversed by the treatment of obesity with metabolic surgery.

As mentioned earlier, it seems clear the relation of an abnor-mally enlarged adipose tissue and oxidative stress as it hasbeen analyzed in the article of Y. Gramlich and coworkers.These authors suggest that obese patients undergoing coro-nary artery bypass grafting showed altered myocardial redoxpatterns, indicating an increased oxidative stress with inade-quate antioxidant compensation. This might explain whypatients with high BMI suffering from coronary artery dis-ease are more susceptible to cardiomyopathy and possibledamage by ischemia and reperfusion, for example, duringcardiac surgery. On the other hand, oxidative stress seemsto be related with diabetic retinopathy, one of the multipleaccompanying side-effects of obesity [6]. In this sense,A. Maugeri and collaborators stated that hyperglycemiaincreased ROS production and alters the DNA methylationprocess, therefore altering the expression of certain genes.They also found in their study that curcumin seems to reduceoxidative stress and improves methylation activities, consid-ering this compound an effective antioxidant to counteractthis condition. In the same area, another potent antioxidantwith self-regenerative properties, nanoparticles of ceriumoxide, was tested by A. Lopez-Pascual and coworkers in threetypes of cells (adipocytes, macrophages, andmyotubes) under

HindawiOxidative Medicine and Cellular LongevityVolume 2019, Article ID 5250816, 2 pageshttps://doi.org/10.1155/2019/5250816

Page 2: Editorial Molecular Basis of the Inflammation …downloads.hindawi.com/journals/omcl/2019/5250816.pdfEditorial Molecular Basis of the Inflammation Related to Obesity Ana B. Crujeiras

proinflammatory conditions. These nanoparticles showed amild insulin-sensitizing effect on murine adipocytes andmyotubes that needs to be further studied. Finally, inanother manuscript, M. Carreira et al. stated that Sirt6expression could be a potential therapeutic target to counter-act obesity-related liver diseases because it is downregulatedby the chronic low-grade inflammation and oxidative stressinduced by excess adiposity.

In conclusion, it is recognized worldwide that the mainpredisposing factors to develop obesity are overconsumptionof calories and sedentary lifestyle, although the reality is quitemore complex [7]. These two options either together or indi-vidually will lead to an abnormal enlarged adipose tissue,accompanied by a proinflammatory status [8]. We haveknown this for many years but without being able to tacklethe epidemy of obesity. Therefore, we need to understandthe molecular pathways involved in this pathological condi-tion to provide new therapeutic tools, being the reason forthis special issue.

Conflicts of Interest

The authors declare that there is no conflict of interestregarding the publication of this editorial.

Ana B. CrujeirasPaul Cordero

Diego F. Garcia-DiazEwa Stachowska

Pedro González-Muniesa

References

[1] World Health Organization, Obesity and Overweight, WHO,2018, https://www.who.int/mediacentre/factsheets/fs311/en/.

[2] NCD Risk Factor Collaboration (NCD-RisC), “Trends in adultbody-mass index in 200 countries from 1975 to 2014: a pooledanalysis of 1698 population-based measurement studies with19·2 million participants,” The Lancet, vol. 387, no. 10026,pp. 1377–1396, 2016.

[3] N. Ouchi, J. L. Parker, J. J. Lugus, and K. Walsh, “Adipokines ininflammation and metabolic disease,” Nature Reviews Immu-nology, vol. 11, no. 2, pp. 85–97, 2011.

[4] P. González-Muniesa, M. A. Mártinez-González, F. B. Hu et al.,“Obesity,” Nature Reviews Disease Primers, vol. 3, article 17034,2017.

[5] P. González-Muniesa, L. Garcia-Gerique, P. Quintero,S. Arriaza, A. Lopez-Pascual, and J. A. Martinez, “Effects ofhyperoxia on oxygen-related inflammation with a focus on obe-sity,” Oxidative Medicine and Cellular Longevity, vol. 2016,Article ID 8957827, 11 pages, 2016.

[6] J. M. Santos, G. Mohammad, Q. Zhong, and R. A. Kowluru,“Diabetic retinopathy, superoxide damage and antioxidants,”Current Pharmaceutical Biotechnology, vol. 12, no. 3, pp. 352–361, 2011.

[7] D. Sellayah, F. R. Cagampang, and R. D. Cox, “On the evolu-tionary origins of obesity: a new hypothesis,” Endocrinology,vol. 155, no. 5, pp. 1573–1588, 2014.

[8] E. P. Williams, M.Mesidor, K. Winters, P. M. Dubbert, and S. B.Wyatt, “Overweight and obesity: prevalence, consequences, andcauses of a growing public health problem,” Current ObesityReports, vol. 4, no. 3, pp. 363–370, 2015.

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