Dietary sugars, not lipids, drive hypothalamic inflammation
Open accessAbstract
OBJECTIVE: The hypothalamus of hypercaloric diet-induced obese animals is featured by a significant increase of microglial reactivity and its associated cytokine production. However, the role of dietary components, in particular fat and carbohydrate, with respect to the hypothalamic inflammatory response and the consequent impact on hypothalamic control of energy homeostasis is yet not clear. METHODS: We dissected the different effects of high-carbohydrate high-fat (HCHF) diets and low-carbohydrate high-fat (LCHF) diets on hypothalamic inflammatory responses in neurons and non-neuronal cells and tested the hypothesis that HCHF diets induce hypothalamic inflammation via advanced glycation end-products (AGEs) using mice lacking advanced glycation end-products (AGEs) receptor (RAGE) and/or the activated leukocyte cell-adhesion molecule (ALCAM). RESULTS: We found that consumption of HCHF diets, but not of LCHF diets, increases microgliosis as well as the presence of N(ε)-(Carboxymethyl)-Lysine (CML), a major AGE, in POMC and NPY neurons of the arcuate nucleus. Neuron-secreted CML binds to both RAGE and ALCAM, which are expressed on endothelial cells, microglia, and pericytes. On a HCHF diet, mice lacking the RAGE and ALCAM genes displayed less microglial reactivity and less neovasculature formation in the hypothalamic ARC, and this was associated with significant improvements of metabolic disorders induced by the HCHF diet. CONCLUSIONS: , leads to excessive CML production in hypothalamic neurons, which, in turn, stimulates hypothalamic inflammatory responses such as microgliosis and eventually leads to neuronal dysfunction in the control of energy metabolism.
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The presence of excess sugar in a high-fat diet was necessary for hypothalamic inflammatory responses in mice, including activation of microglia.
“The presence of excess sugar in a HFD was shown to be necessary for hypothalamic inflammatory responses in mice, including the activation of microglia, the resident immune cells of the brain [58].”
From The menace of obesity to depression and anxiety prevalence (2022) · cites this paper as [58]
AGEs are implicated in the development of numerous chronic diseases including diabetes-related complications, cardiovascular, renal, and neurodegenerative disease, and have recently been implicated in hypothalamic inflammation and obesity.
“Advanced glycation end products (AGEs) are a complex and heterogeneous group of protein, lipid, and DNA adducts implicated in the development of numerous chronic diseases including diabetes related complications, cardiovascular, renal, and neurodegenerative disease, and have recently also been implicated in hypothalamic inflammation and obesity.[1]”
From The Role of Dietary Advanced Glycation End Products in Metabolic Dysfunction (2021) · cites this paper as [1]
AGEs are produced endogenously as part of normal metabolism and during cooking and processing of food, and a significant proportion is absorbed in the gastrointestinal tract.
“AGEs are produced both naturally in the body, as part of normal metabolism, and during the cooking and processing of food with a significant proportion being absorbed in the gastrointestinal tract.”
From The Role of Dietary Advanced Glycation End Products in Metabolic Dysfunction (2021) · cites this paper as [1]
In mice, knockdown of both RAGE and ALCAM was required to block the proinflammatory effects of CML.
“In mice, where AGEs were identified as being the mechanism by which a high-fat diet causes hypothalamic inflammation, knockdown of both RAGE and AL-CAM was required to block the proinflammatory effects of CML.[1]”
From The Role of Dietary Advanced Glycation End Products in Metabolic Dysfunction (2021) · cites this paper as [1]
A diet high in both lipids and carbohydrates is required to induce a significant increase in hypothalamic inflammation in rodents associated with an increase in body weight.
“In support of this, a diet high in both lipids and carbohydrates is required to induce a significant increase in hypothalamic inflammation in rodents associated with an increase in body weight.[1,150]”
From The Role of Dietary Advanced Glycation End Products in Metabolic Dysfunction (2021) · cites this paper as [1]
The high-fat and high-carbohydrate diet also caused an increase in CML immunoreactivity in both POMC and NPY neurons.
“The high-fat and high-carbohydrate diet also caused an increase in CML immunoreactivity in both POMC and NPY neurons.”
From The Role of Dietary Advanced Glycation End Products in Metabolic Dysfunction (2021) · cites this paper as [1]
The role of AGEs in promoting hypothalamic inflammation was confirmed in animals lacking RAGE and ALCAM, which have an improved metabolic phenotype and decreased microglial reactivity on a high-fat diet.
“The role of AGEs in promoting hypothalamic inflammation was confirmed in animals lacking RAGE and ALCAM which have an improved metabolic phenotype and decreased microglial reactivity on a high-fat diet.[1]”
From The Role of Dietary Advanced Glycation End Products in Metabolic Dysfunction (2021) · cites this paper as [1]
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Cites
Zhang, Y., Chen, K., Sloan, S. A., Bennett, M. L., Scholze, A. R., O'Keeffe, S., Phatnani, H. P., Guarnieri, P., Caneda, C., Ruderisch, N., et al. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.1860-14.2014 · Cited by 4,875 · see citing works
Advanced glycation end-products: A review
Singh, R., Barden, A., Mori, T., & Beilin, L. (2001) · Diabetologia · doi:10.1007/s001250051591 · Cited by 2,597 · see citing works
Weight Loss with a Low-Carbohydrate, Mediterranean, or Low-Fat Diet
Shai, I., Schwarzfuchs, D., Henkin, Y., Shahar, D. R., Witkow, S., Greenberg, I., Golan, R., Fraser, D., Bolotin, A., Vardi, H., et al. (2008) · New England Journal of Medicine · doi:10.1056/nejmoa0708681 · Cited by 2,143 · see citing works
Obesity is associated with hypothalamic injury in rodents and humans.
Thaler, J. P., Yi, C.-X., Schur, E. A., Guyenet, S. J., Hwang, B. H., Dietrich, M. O., Zhao, X., Sarruf, D. A., Izgur, V., Maravilla, K. R., et al. (2012) · Journal of Clinical Investigation · doi:10.1172/jci59660 · Cited by 1,857 · see citing works
De Souza, C. T., Araujo, E. P., Bordin, S., Ashimine, R., Zollner, R. L., Boschero, A. C., Saad, M. J. A., & Velloso, L. A. (2005) · Endocrinology · doi:10.1210/en.2004-1520 · Cited by 1,171 · see citing works
Milanski, M., Degasperi, G., Coope, A., Morari, J., Denis, R., Cintra, D. E., Tsukumo, D. M. L., Anhe, G., Amaral, M. E., Takahashi, H. K., et al. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.2760-08.2009 · Cited by 1,125 · see citing works
Dhingra, R., Sullivan, L., Jacques, P. F., Wang, T. J., Fox, C. S., Meigs, J. B., D’Agostino, R. B., Gaziano, J. M., & Vasan, R. S. (2007) · Circulation · doi:10.1161/circulationaha.107.689935 · Cited by 918 · see citing works
Fu, M.-X., Requena, J. R., Jenkins, A. J., Lyons, T. J., Baynes, J. W., & Thorpe, S. R. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.17.9982 · Cited by 822 · see citing works
Sugar consumption, metabolic disease and obesity: The state of the controversy
Stanhope, K. L. (2016) · Critical Reviews in Clinical Laboratory Sciences · doi:10.3109/10408363.2015.1084990 · Cited by 739 · see citing works
Huttunen, H. J., Fages, C., & Rauvala, H. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.28.19919 · Cited by 629 · see citing works
High‐yield isolation of murine microglia by mild trypsinization
Saura, J., Tusell, J. M., & Serratosa, J. (2003) · Glia · doi:10.1002/glia.10274 · Cited by 595 · see citing works
Liliensiek, B., Weigand, M. A., Bierhaus, A., Nicklas, W., Kasper, M. E., Hofer, S., Plachky, J., Gröne, H.-J., Kurschus, F. C., Schmidt, A. M., et al. (2004) · Journal of Clinical Investigation · doi:10.1172/jci18704 · Cited by 525 · see citing works
Effects of β-hydroxybutyrate on cognition in memory-impaired adults
Reger, M. A., Henderson, S. T., Hale, C. M., Cholerton, B., Baker, L. D., Watson, G. S., Hyde, K., Chapman, D., & Craft, S. (2003) · Neurobiology of Aging · doi:10.1016/s0197-4580(03)00087-3 · Cited by 510 · see citing works
Liliensiek, B., Weigand, M. A., Bierhaus, A., et al. (2004) · Journal of Clinical Investigation · doi:10.1172/jci200418704 · Cited by 468 · see citing works
Kirstein, M., Brett, J., Radoff, S., Ogawa, S., Stern, D., & Vlassara, H. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.22.9010 · Cited by 364 · see citing works
Guijarro-Muñoz, I., Compte, M., Álvarez-Cienfuegos, A., Álvarez-Vallina, L., & Sanz, L. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.521161 · Cited by 342 · see citing works
Detecting protein–protein interactions by far western blotting
Wu, Y., Li, Q., & Chen, X. (2007) · Nature Protocols · doi:10.1038/nprot.2007.459 · Cited by 334 · see citing works
Schmidt, A. M., Hasu, M., Popov, D., Zhang, J. H., Chen, J., Yan, S. D., Brett, J., Cao, R. Y., Kuwabara, K., & Costache, G. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.19.8807 · Cited by 327 · see citing works
Treatment of Parkinson disease with diet-induced hyperketonemia: A feasibility study
VanItallie, T. B., Nonas, C., Rocco, A. D., Boyar, K. L., Hyams, K., & Heymsfield, S. B. (2005) · Neurology · doi:10.1212/01.wnl.0000152046.11390.45 · Cited by 300 · see citing works
Dietary fat, fatty acid composition in plasma and the metabolic syndrome
Vessby, B. (2003) · Current Opinion in Lipidology · doi:10.1097/00041433-200302000-00004 · Cited by 291 · see citing works
Diano, S., Liu, Z.-W., Jeong, J. K., Dietrich, M. O., Ruan, H., Kim, E., Suyama, S., Kelly, K., Gyengési, E., Arbiser, J. L., et al. (2011) · Nature Medicine · doi:10.1038/nm.2421 · Cited by 268 · see citing works
Hormones and diet, but not body weight, control hypothalamic microglial activity
Gao, Y., Ottaway, N., Schriever, S. C., Legutko, B., García‐Cáceres, C., de la Fuente, E., Mergen, C., Bour, S., Thaler, J. P., Seeley, R. J., et al. (2013) · Glia · doi:10.1002/glia.22580 · Cited by 265 · see citing works
Requena, J. R., Fu, M.-X., Ahmed, M., Jenkins, A. J., Lyons, T. J., & Thorpe, S. R. (1996) · Nephrology Dialysis Transplantation · doi:10.1093/ndt/11.supp5.48 · Cited by 253 · see citing works
RAGE Regulates the Metabolic and Inflammatory Response to High-Fat Feeding in Mice
Song, F., del Pozo, C. H., Rosario, R., Zou, Y. S., Ananthakrishnan, R., Xu, X., Patel, P. R., Benoit, V. M., Yan, S. F., Li, H., et al. (2014) · Diabetes · doi:10.2337/db13-1636 · Cited by 205 · see citing works
Murata, T., Nagai, R., Ishibashi, T., Inomata, H., Ikeda, K., & Horiuchi, S. (1997) · Diabetologia · doi:10.1007/s001250050747 · Cited by 201 · see citing works
Inhibiting microglia expansion prevents diet-induced hypothalamic and peripheral inflammation
André, C., Guzman-Quevedo, O., Rey, C., Rémus-Borel, J., Clark, S., Castellanos-Jankiewicz, A., Ladeveze, E., Leste-Lasserre, T., Nadjar, A., Abrous, D. N., et al. (2017) · Diabetes · doi:10.2337/db16-0586 · Cited by 182 · see citing works
Hypothalamic innate immune reaction in obesity
Kälin, S., Heppner, F. L., Bechmann, I., Prinz, M., Tschöp, M. H., & Yi, C.-X. (2015) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2015.48 · Cited by 167 · see citing works
Self-citationA versatile ultra-high performance LC-MS method for lipid profiling
Knittelfelder, O. L., Weberhofer, B. P., Eichmann, T. O., Kohlwein, S. D., & Rechberger, G. N. (2014) · Journal of Chromatography B · doi:10.1016/j.jchromb.2014.01.011 · Cited by 161 · see citing works
Sessa, L., Gatti, E., Zeni, F., Antonelli, A., Catucci, A., Koch, M., Pompilio, G., Fritz, G., Raucci, A., & Bianchi, M. E. (2014) · PLoS ONE · doi:10.1371/journal.pone.0086903 · Cited by 153 · see citing works
Dietary treatment in adults with refractory epilepsy
Klein, P., Tyrlíková, I., & Mathews, G. C. (2014) · Neurology · doi:10.1212/wnl.0000000000001004 · Cited by 129 · see citing works
Blázquez, C., Woods, A., CEBALLOS, M. L. D., Carling, D., & Guzmán, M. (1999) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1999.731674.x · Cited by 129 · see citing works
Arachidonic Acid Metabolism as a Potential Mediator of Cardiac Fibrosis Associated with Inflammation
Levick, S. P., Loch, D. C., Taylor, S. M., & Janicki, J. S. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.178.2.641 · Cited by 116 · see citing works
Dysfunction of brain pericytes in chronic neuroinflammation
Persidsky, Y., Hill, J., Zhang, M., Dykstra, H., Winfield, M., Reichenbach, N. L., Potula, R., Mukherjee, A., Ramirez, S. H., & Rom, S. (2016) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x15606149 · Cited by 116 · see citing works
Brain Pericytes: Emerging Concepts and Functional Roles in Brain Homeostasis
Kamouchi, M., Ago, T., & Kitazono, T. (2010) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-010-9605-x · Cited by 92 · see citing works
Bielohuby, M., Menhofer, D., Kirchner, H., Stoehr, B. J. M., Müller, T. D., Stock, P., Hempel, M., Stemmer, K., Pfluger, P. T., Kienzle, E., et al. (2010) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00478.2010 · Cited by 88 · see citing works
High calorie diet triggers hypothalamic angiopathy
Yi, C., Gericke, M. T., Krüger, M., Alkemade, A., Kabra, D. G., Hanske, S., Filosa, J. A., Pfluger, P. T., Bingham, N. C., Woods, S. C., et al. (2012) · Molecular Metabolism · doi:10.1016/j.molmet.2012.08.004 · Cited by 71 · see citing works
Luo, J. J., Wallace, W., Riccioni, T., Ingram, D. K., Roth, G. S., & Kusiak, J. W. (1999) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(19990301)55:5 · Cited by 39 · see citing works
Mobbs, C. V., Mastaitis, J. W., Yen, K., Schwartz, J. E., Mohan, V., Poplawski, M. M., & Isoda, F. (2006) · Appetite · doi:10.1016/j.appet.2006.06.007 · Cited by 39 · see citing works
Low-carbohydrate, high-fat diets have sex-specific effects on bone health in rats
Zengin, A., Kropp, B., Chevalier, Y., Junnila, R. K., Sustarsic, E. G., Herbach, N., Fanelli, F., Mezzullo, M., Milz, S., Bidlingmaier, M., et al. (2015) · European Journal of Nutrition · doi:10.1007/s00394-015-1040-9 · Cited by 27 · see citing works
Hepatic disposal of advanced glycation end products during maturation and aging
Svistounov, D., Oteiza, A., Zykova, S. N., Sørensen, K. K., McCourt, P., McLachlan, A. J., McCuskey, R. S., & Smedsrød, B. H. (2013) · Experimental Gerontology · doi:10.1016/j.exger.2013.03.005 · Cited by 25 · see citing works
Treatment of Parkinson disease with diet-induced hyperketonemia: A feasibility study
Jabre, M., & Bejjani, B.-P. W. (2006) · Neurology · doi:10.1212/01.wnl.0000216108.57529.b1 · Cited by 24 · see citing works
Forsberg‐Nilsson, K., Erlandsson, A., Zhang, X., Ueda, H., Svensson, K., Nistér, M., Trapp, B. D., Peterson, A. C., & Westermark, B. (2003) · Glia · doi:10.1002/glia.10191 · Cited by 22 · see citing works
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The menace of obesity to depression and anxiety prevalence
Fulton, S., Décarie-Spain, L., Fioramonti, X., Guiard, B., & Nakajima, S. (2022) · Trends in Endocrinology & Metabolism · doi:10.1016/j.tem.2021.10.005 · Cited by 441 · see citing works
“The presence of excess sugar in a HFD was shown to be necessary for hypothalamic inflammatory responses in mice, including the activation of microglia, the resident immune cells of the brain [58].”
BackgroundRole of astrocytes, microglia, and tanycytes in brain control of systemic metabolism
García‐Cáceres, C., Balland, É., Prévot, V., Luquet, S. H., Woods, S. C., Koch, M., Horváth, T. L., Yi, C., Chowen, J. A., Verkhratsky, A., et al. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0286-y · Cited by 326 · see citing works
Role of c-Jun N-terminal Kinase (JNK) in Obesity and Type 2 Diabetes
Yung, J. H. M., & Giacca, A. (2020) · Cells · doi:10.3390/cells9030706 · Cited by 274 · see citing works
Inflammageing and metaflammation: The yin and yang of type 2 diabetes
Prattichizzo, F., Nigris, V. D., Spiga, R., Mancuso, E., Sala, L. L., Antonicelli, R., Testa, R., Procopio, A. D., Olivieri, F., & Ceriello, A. (2017) · Ageing Research Reviews · doi:10.1016/j.arr.2017.10.003 · Cited by 249 · see citing works
The Role of Dietary Advanced Glycation End Products in Metabolic Dysfunction
Sergi, D., Boulestin, H., Campbell, F. M., & Williams, L. M. (2021) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201900934 · Cited by 194 · see citing works
Raichur, S., Brunner, B., Bielohuby, M., Hansen, G., Pfenninger, A., Wang, B., Brüning, J. C., Larsen, P. J., & Tennagels, N. (2019) · Molecular Metabolism · doi:10.1016/j.molmet.2018.12.008 · Cited by 194 · see citing works
Hypothalamic inflammation and obesity: a mechanistic review
Seong, J., Kang, J. Y., Sun, J. S., & Kim, K. W. (2019) · Archives of Pharmacal Research · doi:10.1007/s12272-019-01138-9 · Cited by 158 · see citing works
Sarcopenia: Etiology, Nutritional Approaches, and miRNAs
Cannataro, R., Carbone, L., Petro, J. L., Cione, E., Vargas-Molina, S., Romero, H. M. A., Forero, D. A., Odriozola-Martínez, A., Kreider, R. B., & Bonilla, D. A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22189724 · Cited by 167 · see citing works
Nutritional Interventions for Treating Cancer-Related Fatigue: A Qualitative Review
Inglis, J. E., Lin, P., Kerns, S. L., Kleckner, I. R., Kleckner, A. S., Castillo, D. A., Mustian, K. M., & Peppone, L. J. (2019) · Nutrition and Cancer · doi:10.1080/01635581.2018.1513046 · Cited by 135 · see citing works
“Hypothalamic Microinflammation” Paradigm in Aging and Metabolic Diseases
Cai, D., & Khor, S. (2019) · Cell Metabolism · doi:10.1016/j.cmet.2019.05.021 · Cited by 134 · see citing works
Molecular Mechanisms of Hypothalamic Insulin Resistance
Ono, H. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20061317 · Cited by 107 · see citing works
Vargas-Soria, M., Garcı́a-Alloza, M., & Corraliza-Gómez, M. (2023) · Journal of Neuroinflammation · doi:10.1186/s12974-023-02740-x · Cited by 109 · see citing works
The hypothalamus for whole-body physiology: from metabolism to aging
Liu, T., Xu, Y., Yi, C., Tong, Q., & Cai, D. (2021) · Protein & Cell · doi:10.1007/s13238-021-00834-x · Cited by 103 · see citing works
Grandl, G., Straub, L., Rudigier, C., Arnold, M., Wueest, S., Konrad, D., & Wolfrum, C. (2018) · The Journal of Physiology · doi:10.1113/jp275173 · Cited by 97 · see citing works
Role of advanced glycation end products and insulin resistance in diabetic nephropathy
Parwani, K., & Mandal, P. (2020) · Archives of Physiology and Biochemistry · doi:10.1080/13813455.2020.1797106 · Cited by 97 · see citing works
Diabetes, a Contemporary Risk for Parkinson’s Disease: Epidemiological and Cellular Evidences
Sergi, D., Renaud, J., Simola, N., & Martinoli, M. (2019) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2019.00302 · Cited by 85 · see citing works
Hypothalamic inflammation in metabolic disorders and aging
Bhusal, A., Rahman, M. H., & Suk, K. (2021) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-021-04019-x · Cited by 79 · see citing works
The Significance of Hypothalamic Inflammation and Gliosis for the Pathogenesis of Obesity in Humans
SEWAYBRICKER, L. E., Huang, A., Chandrasekaran, S., Melhorn, S. J., & Schur, E. A. (2022) · Endocrine Reviews · doi:10.1210/endrev/bnac023 · Cited by 73 · see citing works
Cansell, C., Stobbe, K., Sanchez, C., Thuc, O. L., Mosser, C., Fradj, S. B., Leredde, J., Lebeaupin, C., Debayle, D., Fleuriot, L., et al. (2020) · Glia · doi:10.1002/glia.23882 · Cited by 69 · see citing works
Cordova, R., Knaze, V., Viallon, V., Rust, P., Schalkwijk, C. G., Weiderpass, E., Wagner, K.-H., Mayen-Chacon, A.-L., Aglago, E. K., Dahm, C. C., et al. (2020) · European Journal of Nutrition · doi:10.1007/s00394-019-02129-8 · Cited by 62 · see citing works
Pflimlin, E., Bielohuby, M., Korn, M., Breitschopf, K., Löhn, M., Wohlfart, P., Konkar, A. A., Podeschwa, M. A. L., Bärenz, F., Pfenninger, A., et al. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2018.05.028 · Cited by 61 · see citing works
Nutrition as Metabolic Treatment for Anxiety
Norwitz, N. G., & Naidoo, U. (2021) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2021.598119 · Cited by 63 · see citing works
Rahman, M. H., Bhusal, A., Lee, W., Lee, I., & Suk, K. (2018) · Biochemical Pharmacology · doi:10.1016/j.bcp.2018.01.024 · Cited by 57 · see citing works
Low-Fat Diet With Caloric Restriction Reduces White Matter Microglia Activation During Aging
Yin, Z., Raj, D. D. A., Schaafsma, W., van der Heijden, R. A., Kooistra, S. M., Reijne, A. C., Zhang, X., Moser, J., Brouwer, N., Heeringa, P., et al. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00065 · Cited by 56 · see citing works
Cell and molecular mechanisms behind diet‐induced hypothalamic inflammation and obesity
Ávalos, Y., Kerr, B., Maliqueo, M. A., & Dorfman, M. D. (2018) · Journal of Neuroendocrinology · doi:10.1111/jne.12598 · Cited by 53 · see citing works
Amor, S., González‐Hedström, D., Martín-Carro, B., Inarejos-García, A. M., Almodóvar, P., Pródanov, M., Garcı́a-Villalón, Á. L., & Granado, M. (2019) · Nutrients · doi:10.3390/nu11010153 · Cited by 54 · see citing works
Diet-Induced Obesity Disturbs Microglial Immunometabolism in a Time-of-Day Manner
Milanova, I. V., Kalsbeek, M. J. T., Wang, X.-L., Korpel, N. L., Stenvers, D. J., Wolff, S. E. C., de Goede, P., Heijboer, A. C., Fliers, E., la Fleur, S. E., et al. (2019) · Frontiers in Endocrinology · doi:10.3389/fendo.2019.00424 · Cited by 53 · see citing works
Hypothalamic microglia as potential regulators of metabolic physiology.
Valdearcos, M., Myers, M. G., & Koliwad, S. K. (2019) · Nature Metabolism · doi:10.1038/s42255-019-0040-0 · Cited by 52 · see citing works
Wang, Q., Lu, M., Zhu, X., Gu, X., Zhang, T., Xia, C., Yang, L., Xu, Y., & Zhou, M. (2022) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2022.113412 · Cited by 52 · see citing works
A high-fat diet induces rapid changes in the mouse hypothalamic proteome
McLean, F. H., Campbell, F., Langston, R. F., Sergi, D., Resch, C., Grant, C., Morris, A. C., Mayer, C., & Williams, L. M. (2019) · Nutrition & Metabolism · doi:10.1186/s12986-019-0352-9 · Cited by 49 · see citing works
Sergi, D., & Williams, L. M. (2019) · Nutrition Reviews · doi:10.1093/nutrit/nuz056 · Cited by 47 · see citing works
Yeh, S. H., Shie, F., Liu, H., Yao, H.-H., Kao, P.-C., Lee, Y.-H., Chen, L.-M., Hsu, S.-M., Chao, L.-J., Wu, K.-W., et al. (2019) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2019.11.018 · Cited by 45 · see citing works
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Selman, A., Dai, J., Driskill, J., Reddy, A. P., & Reddy, P. H. (2024) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2024.167561 · Cited by 46 · see citing works
Foll, C. L. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.01036 · Cited by 43 · see citing works
Is human obesity an inflammatory disease of the hypothalamus?
Sonnefeld, L., Rohmann, N., Geisler, C., & Laudes, M. (2023) · European Journal of Endocrinology · doi:10.1093/ejendo/lvad030 · Cited by 47 · see citing works
Ketogenic Ratio Determines Metabolic Effects of Macronutrients and Prevents Interpretive Bias
Zilberter, T., & Zilberter, Y. (2018) · Frontiers in Nutrition · doi:10.3389/fnut.2018.00075 · Cited by 43 · see citing works
The Impact of the Ketogenic Diet on Glial Cells Morphology. A Quantitative Morphological Analysis
Gzieło, K., Sołtys, Z., Rajfur, Z., & Setkowicz, Z. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.06.009 · Cited by 41 · see citing works
Trapped fat: Obesity pathogenesis as an intrinsic disorder in metabolic fuel partitioning
Friedman, M. I., Sørensen, T. I. A., Taubes, G., Lund, J. T., & Ludwig, D. S. (2024) · Obesity Reviews · doi:10.1111/obr.13795 · Cited by 45 · see citing works
The Effect of Rev-erbα Agonist SR9011 on the Immune Response and Cell Metabolism of Microglia
Wolff, S. E. C., Wang, X., Jiao, H., Sun, J. Y., Kalsbeek, A., Yi, C., & Gao, Y. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.550145 · Cited by 38 · see citing works
Beaulieu, J., Costa, G., Renaud, J., Moitié, A., Glémet, H., Sergi, D., & Martinoli, M. (2021) · Molecular Neurobiology · doi:10.1007/s12035-021-02328-7 · Cited by 37 · see citing works
Reversal of prolonged obesity-associated cerebrovascular dysfunction by inhibiting microglial Tak1
Shen, Q. X., Chen, Z., Zhao, F., Pan, S., Zhang, T., Cheng, X., Zhang, L., Zhang, S., Qi, J., Li, J., et al. (2020) · Nature Neuroscience · doi:10.1038/s41593-020-0642-6 · Cited by 38 · see citing works
Valentin‐Escalera, J., Leclerc, M., & Calon, F. (2024) · Journal of Alzheimer s Disease · doi:10.3233/jad-230118 · Cited by 35 · see citing works
Hypothalamic Astrocytes as a Specialized and Responsive Cell Population in Obesity
González‐García, I., & García‐Cáceres, C. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22126176 · Cited by 34 · see citing works
Demirer, B., Yardımcı, H., & Basmaz, S. E. (2022) · Journal of Diabetes and its Complications · doi:10.1016/j.jdiacomp.2022.108354 · Cited by 35 · see citing works
Immunometabolic Changes in Glia – A Potential Role in the Pathophysiology of Obesity and Diabetes
Robb, J. L., Morrissey, N. A., Potter, P. G. W., Smithers, H. E., Beall, C., & Ellacott, K. L. J. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.10.021 · Cited by 35 · see citing works
Barlampa, D., Bompoula, M. S., Bargiota, Α., Kalantaridou, S., Mastorakos, G. P., & Valsamakis, G. (2021) · Nutrients · doi:10.3390/nu13020520 · Cited by 37 · see citing works
Niño, O. M. S., da Costa, C. S., Torres, K. M., Zanol, J. F., Freitas‐Lima, L. C., Miranda‐Alves, L., & Graceli, J. B. (2020) · Toxicology Letters · doi:10.1016/j.toxlet.2020.07.002 · Cited by 32 · see citing works
Hypothalamic microinflammation
Cai, D., & Khor, S. (2021) · Handbook of clinical neurology · doi:10.1016/b978-0-12-820683-6.00023-3 · Cited by 31 · see citing works
Microglia shape AgRP neuron postnatal development via regulating perineuronal net plasticity
Sun, J. Y., Wang, X., Sun, R., Xiao, X., Wang, Y., Peng, Y., & Gao, Y. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02326-2 · Cited by 29 · see citing works
Suriano, F., Vieira‐Silva, S., Falony, G., d’Oplinter, A. D. W., Paone, P., Delzenne, N. M., Everard, A., Raes, J., Hul, M. V., & Cani, P. D. (2022) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00141.2022 · Cited by 29 · see citing works
Al-Nimr, R. I., Wright, K. C. S., Aquila, C. L., Petersen, C. L., Gooding, T., & Batsis, J. A. (2020) · Clinical Nutrition ESPEN · doi:10.1016/j.clnesp.2020.09.002 · Cited by 28 · see citing works
Sohouli, M. H., Sharifi‐Zahabi, E., Lari, A., Fatahi, S., & Shidfar, F. (2020) · Scientific Reports · doi:10.1038/s41598-020-79216-y · Cited by 28 · see citing works
Labandeira, C. M., Bau, A. F., Ron, D. A., Muñoz, A., Losada, G. A., Koukoulis, A., Romero-López, J., & Rodriguez-Perez, A. I. (2021) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2021.100914 · Cited by 28 · see citing works
Arcuate Nucleus of the Hypothalamus: Anatomy, Physiology, and Diseases
Song, J., & Choi, S. (2023) · Experimental Neurobiology · doi:10.5607/en23040 · Cited by 32 · see citing works
Low-carbohydrate, high-fat diets have sex-specific effects on bone health in rats
Zengin, A., Kropp, B., Chevalier, Y., Junnila, R. K., Sustarsic, E. G., Herbach, N., Fanelli, F., Mezzullo, M., Milz, S., Bidlingmaier, M., et al. (2015) · European Journal of Nutrition · doi:10.1007/s00394-015-1040-9 · Cited by 27 · see citing works
Zanol, J. F., Niño, O. M. S., da Costa, C. S., Freitas‐Lima, L. C., Miranda‐Alves, L., & Graceli, J. B. (2021) · Reproductive Toxicology · doi:10.1016/j.reprotox.2021.06.004 · Cited by 26 · see citing works
Mandwie, M., Karunia, J., Niaz, A., Keay, K. A., Musumeci, G., Rennie, C., McGrath, K. C. Y., Al‐Badri, G., & Castorina, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222413660 · Cited by 25 · see citing works
Metabolic factors in the regulation of hypothalamic innate immune responses in obesity
Folick, A., Cheang, R. T., Valdearcos, M., & Koliwad, S. K. (2022) · Experimental & Molecular Medicine · doi:10.1038/s12276-021-00666-z · Cited by 22 · see citing works
Microglia–Neuron Crosstalk in Obesity: Melodious Interaction or Kiss of Death?
Leon, S., Nadjar, A., & Quarta, C. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22105243 · Cited by 20 · see citing works
Senatus, L. M., MacLean, M., Arivazhagan, L., Egaña-Gorroño, L., López‐Díez, R., Manigrasso, M. B., Ruiz, H. H., Vásquez, C., Wilson, R. A., Shekhtman, A. G., et al. (2021) · Immunometabolism · doi:10.20900/immunometab20210024 · Cited by 20 · see citing works
Exercise Restores Hypothalamic Health in Obesity by Reshaping the Inflammatory Network
Guardia, L. D., & Codella, R. (2023) · Antioxidants · doi:10.3390/antiox12020297 · Cited by 21 · see citing works
Belegri, E., Eggels, L., Unmehopa, U. A., Mul, J. D., Boelen, A., & la Fleur, S. E. (2017) · Appetite · doi:10.1016/j.appet.2017.10.006 · Cited by 19 · see citing works
Loss of Microglial Insulin Receptor Leads to Sex-Dependent Metabolic Disorders in Obese Mice
Milanova, I. V., Korpel, N. L., Corrêa‐da‐Silva, F., Berends, E., Osman, S., la Fleur, S. E., Fliers, E., Kalsbeek, A., & Yi, C. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23062933 · Cited by 18 · see citing works
Microglia in Central Control of Metabolism
Kim, J. D., Copperi, F., & Diano, S. (2023) · Physiology · doi:10.1152/physiol.00021.2023 · Cited by 20 · see citing works
Mapping of Microglial Brain Region, Sex and Age Heterogeneity in Obesity
Milanova, I. V., Corrêa‐da‐Silva, F., Kalsbeek, A., & Yi, C. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22063141 · Cited by 18 · see citing works
Hypothalamic Inflammation at a Crossroad of Somatic Diseases
Mravec, B., Horváthová, Ľ., & Černáčková, A. (2018) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-018-0631-4 · Cited by 17 · see citing works
The timeline of neuronal and glial alterations in experimental obesity
Engel, D. F., & Velloso, L. A. (2022) · Neuropharmacology · doi:10.1016/j.neuropharm.2022.108983 · Cited by 17 · see citing works
Dietary fat: a potent microglial influencer
Ceasrine, A. M., & Bilbo, S. D. (2022) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2021.12.005 · Cited by 16 · see citing works
Advanced glycation end products and insulin resistance in diabetic nephropathy
Parwani, K., & Mandal, P. (2024) · Vitamins and hormones · doi:10.1016/bs.vh.2024.02.007 · Cited by 19 · see citing works
High‐fat diet‐induced elevation of body weight set point in male mice
Fang, L. Z., Vidal, J. A. L., Hawlader, O., & Hirasawa, M. (2023) · Obesity · doi:10.1002/oby.23650 · Cited by 15 · see citing works
Microgliosis: a double‐edged sword in the control of food intake
Salvi, J., Andreoletti, P., Audinat, É., Balland, É., Fradj, S. B., Cherkaoui‐Malki, M., Heurtaux, T., Liénard, F., Nédélec, E., Rovère, C., et al. (2022) · FEBS Journal · doi:10.1111/febs.16583 · Cited by 12 · see citing works
MiR-146a-5p Contributes to Microglial Polarization Transitions Associated With AGEs
Huang, Y., Lin, X., & Lin, X. (2023) · Molecular Neurobiology · doi:10.1007/s12035-023-03252-8 · Cited by 12 · see citing works
Gamede, M. W., Mabuza, L. P., Ngubane, P. S., & Khathi, A. (2020) · Therapeutic Advances in Endocrinology and Metabolism · doi:10.1177/2042018820935771 · Cited by 12 · see citing works
A primer on metabolic memory: why existing diabesity treatments fail
Çöpür, S., Rossing, P. R., Afşar, B., Sag, A. A., Siriopol, D. C., Kuwabara, M., Ortíz, A., & Kanbay, M. (2020) · Clinical Kidney Journal · doi:10.1093/ckj/sfaa143 · Cited by 10 · see citing works
Trends in Gliosis in Obesity, and the Role of Antioxidants as a Therapeutic Alternative
Bandala, C., Cárdenas‐Rodríguez, N., Reyes-Long, S., Cortes-Altamirano, J. L., Garciadiego-Cázares, D., Lara‐Padilla, E., Ibáñez-Cervantes, G., Mancilla-Ramı́rez, J., Gómez‐Manzo, S., & Alfaro-Rodríguez, A. (2022) · Antioxidants · doi:10.3390/antiox11101972 · Cited by 10 · see citing works
Eustress, distress, and oxidative stress: Promising pathways for mind-body medicine
Aschbacher, K., & Mason, A. E. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-818606-0.00029-8 · Cited by 10 · see citing works
TSPO: an emerging role in appetite for a therapeutically promising biomarker
Wang, J., & Beecher, K. (2021) · Open Biology · doi:10.1098/rsob.210173 · Cited by 10 · see citing works
Carr, K. D., Weiner, S. P., Vásquez, C., & Schmidt, A. M. (2023) · Physiology & Behavior · doi:10.1016/j.physbeh.2023.114337 · Cited by 10 · see citing works
Zagmutt, S., Rodriguez-Garcia, M., Bolaños-Hurtado, M., Reguera, A. C., Casals, N., & Rodríguez‐Rodríguez, R. (2025) · Reviews in Endocrine and Metabolic Disorders · doi:10.1007/s11154-025-09992-3 · Cited by 9 · see citing works
Cheng, M. Z. S. Z., Amin, F. A. Z., Zawawi, N., Chan, K. W., Ismail, N., Ishak, N. A., & Norhaizan, M. E. (2023) · Nutrients · doi:10.3390/nu15132835 · Cited by 8 · see citing works
Patil, N. A., Kelkar, A., & Sivaram, A. (2022) · BioNanoScience · doi:10.1007/s12668-022-00954-6 · Cited by 8 · see citing works
Possible effects of dietary advanced glycation end products on maternal and fetal health: a review
Demirer, B., & Samur, G. (2022) · Nutrition Reviews · doi:10.1093/nutrit/nuac090 · Cited by 7 · see citing works
Hypothalamic astrocytes: connecting brain and periphery in metabolic control
Thuc, O. L., Lechner, F. M., & García‐Cáceres, C. (2025) · Reviews in Endocrine and Metabolic Disorders · doi:10.1007/s11154-025-09995-0 · Cited by 6 · see citing works
Obesity-mediated Lipoinflammation Modulates Food Reward Responses
Huerta, C., Caba, M., & Camacho‐Morales, A. (2023) · Neuroscience · doi:10.1016/j.neuroscience.2023.08.019 · Cited by 6 · see citing works
A dahlia flower extract has antidiabetic properties by improving insulin function in the brain
Pretz, D., Heyward, P. M., Krebs, J. D., Gruchot, J., Barter, C., Silcock, P. J., Downes, N., Rizwan, M. Z., Boucsein, A., Bender, J., et al. (2023) · Life Metabolism · doi:10.1093/lifemeta/load026 · Cited by 5 · see citing works
Dual functions of CNS inflammation in food intake and metabolic regulation
Lee, T.-J., Hargrave, S. L., & Kinzig, K. P. (2020) · Brain Research · doi:10.1016/j.brainres.2020.146859 · Cited by 4 · see citing works
Control of Systemic Metabolism by Astrocytes in the Brain
Thuc, O. L., Gruber, T., Tschöp, M. H., & García‐Cáceres, C. (2021) · Masterclass in neuroendocrinology · doi:10.1007/978-3-030-62383-8_6 · Cited by 5 · see citing works
Breuer, S., Kasper, P., Vohlen, C., Janoschek, R., Hoffmann, T., Appel, S., Müller-Limberger, E., Mesaros, A., Rose‐John, S., Garbers, C., et al. (2021) · Nutrients · doi:10.3390/nu13113735 · Cited by 5 · see citing works
Update on Hypothalamic Inflammation and Gliosis: Expanding Evidence of Relevance Beyond Obesity
Huang, A., Yeum, D., SEWAYBRICKER, L. E., Aleksić, S., Thomas, M., Melhorn, S. J., Feng, Y., & Schur, E. A. (2025) · Current Obesity Reports · doi:10.1007/s13679-024-00595-8 · Cited by 5 · see citing works
Tabar, M. S., Nilghaz, M., Hekmatdoost, A., Pashayee-Khamene, F., Mokhtari, Z., Karimi, S., Ahmadzadeh, S., Saberifiroozi, M., Hatami, B., & Yari, Z. (2025) · Scientific Reports · doi:10.1038/s41598-025-89433-y · Cited by 4 · see citing works
Neurovascular plasticity as a modulator of hypothalamic function
Chen, B., Furtado, J., & Schneeberger, M. (2025) · Reviews in Endocrine and Metabolic Disorders · doi:10.1007/s11154-025-09982-5 · Cited by 6 · see citing works
Dakic, T. B., Lakic, I. V., Zec, M. M., Takić, M. M., Stojiljković, M., & Jevdjovic, T. V. (2021) · Journal of the Science of Food and Agriculture · doi:10.1002/jsfa.11252 · Cited by 4 · see citing works
Astrocytes in neural circuits controlling appetite and food intake
Ellacott, K. L. J. (2021) · Current Opinion in Endocrine and Metabolic Research · doi:10.1016/j.coemr.2021.100313 · Cited by 4 · see citing works
Weight loss aggravates obesity-induced hypothalamic inflammation in mid-aged mice
Zemer, A., Haim, Y., Tsitrina, A. A., Caspi, V. C., Muallem, H., Pincu, Y., Wong, G. W., Yoel, U., Monsonego, A., & Rudich, A. (2025) · GeroScience · doi:10.1007/s11357-025-01933-x · Cited by 3 · see citing works
Debras, C., Córdova, R., Mayén, A., Maasen, K., Knaze, V., Eussen, S. J. P. M., Schalkwijk, C. G., Huybrechts, I., Tjønneland, A. M., Halkjær, J., et al. (2024) · British Journal Of Nutrition · doi:10.1017/s0007114524000503 · Cited by 3 · see citing works
Stress and Microglia: A Double-edged Relationship
Delpech, J.-C., Valdearcos, M., & Nadjar, A. (2024) · Advances in neurobiology · doi:10.1007/978-3-031-55529-9_18 · Cited by 3 · see citing works
Campanile, A. A., & Eckel, L. A. (2025) · Cells · doi:10.3390/cells14030233 · Cited by 3 · see citing works
Buckner, T., Johnson, R. K., Vanderlinden, L. A., Carry, P. M., Romero, A., Önengüt-Gümüşcü, S., Chen, W., Fiehn, O., Frohnert, B. I., Crume, T., et al. (2023) · Nutrients · doi:10.3390/nu15040945 · Cited by 4 · see citing works
Fat food exacerbates post-prandial hypothalamic inflammation involving GFAP+ cells and microgliaPreprint
Cansell, C., Stobbe, K., Thuc, O. L., Mosser, C., Fradj, S. B., Leredde, J., Lebeaupin, C., Debayle, D., Fleuriot, L., Brau, F., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/835967 · Cited by 3 · see citing works
- Authors
- Gao, Y., Bielohuby, M., Fleming, T., Grabner, G. F., Foppen, E., Bernhard, W., Guzmán-Ruiz, M., Layritz, C., Legutko, B., Zinser, E., García-Cáceres, C., Buijs, R. M., Woods, S. C., Kalsbeek, A., Seeley, R. J., Nawroth, P. P., Bidlingmaier, M., Tschöp, M. H., & Yi, C.-X.
- Affiliations
- Amsterdam UMC Location University of Amsterdam (NL)
- LMU Klinikum (DE)
- University Hospital Heidelberg (DE)
- University of Graz (AT)
- Helmholtz Munich (DE)
- FH JOANNEUM University of Applied Sciences (AT)
- Universidad Nacional Autónoma de México (MX)
- University of Cincinnati (US)
- Netherlands Institute for Neuroscience (NL)
- University of Michigan (US)
- Corresponding author
- Bidlingmaier, Martin
- Tschöp, Matthias H.
- Yi, Chun-Xia
- ORCID
- Venue
- Molecular Metabolism
- Publisher
- Elsevier BV
- Published
- 2017-08
- Volume
- 6
- Issue
- 8
- Pages
- 897-908
- ISSN
- 2212-8778 (ISSN-L)
- PMC
- PMC5518723
- OpenAlex
- W2652575518
- Cited by
- 131
- References
- 41
- Citations by year
- 2026: 6 · 2025: 10 · 2024: 12 · 2023: 15 · 2022: 18 · 2021: 23 · 2020: 13 · 2019: 22 · 2018: 9 · 2017: 2 · 2015: 1
- FWCI
- 6.27
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Molecular Metabolism (publishedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- Pure Amsterdam UMC (publishedVersion, other-oa)
- KNAW Research Portal (The Royal Netherlands Academy of Arts and Sciences) (publishedVersion, other-oa)
- FH JOANNEUM ePUB (submittedVersion, cc-by-nc-nd)
- PuSH - Publication Server of Helmholtz Zentrum München (submittedVersion, cc-by-nc-nd)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- Data Archiving and Networked Services (DANS) (submittedVersion, other-oa)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- Open access LMU (Ludwid Maxmilian's Universitat Munchen) (submittedVersion, cc-by-nc-nd)
- mediaTUM (Technical University of Munich) (submittedVersion)
- Site cant be reached (submittedVersion, cc-by-nc-nd)
- Funders
- Daiichi-Sankyo
- Alexander von Humboldt-Stiftung
- Deutsche Forschungsgemeinschaft (SFB1123, ANR- 15-CE14-0030, SFB1118)
- U.S. Department of Homeland Security
- Novartis
- Novo Nordisk
- Academisch Medisch Centrum
- Helmholtz Association
- European Research Council (695054)
- Topics
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Regulation of Appetite and Obesity
- Health Sciences › Medicine › Epidemiology › Adipokines, Inflammation, and Metabolic Diseases
- Keywords
- hypothalamic inflammation, dietary sugar, high-fat high-carbohydrate diet, advanced glycation end products, carboxymethyllysine, microglial activation, RAGE, ALCAM, arcuate nucleus, POMC neurons, NPY neurons, neovasculature, energy homeostasis, obesity, hypercaloric diet, endothelial cells, pericytes
- MeSH terms
- Receptor for Advanced Glycation End Products, Dietary Sugars, Animals, Dietary Fats, Gliosis, Hypothalamus, Inflammation, Male, Mice, Inbred C57BL, Glycation End Products, Advanced, Activated-Leukocyte Cell Adhesion Molecule, Mice, Rats
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