The effect of experimental diabetes on high mobility group box 1 protein expression in endotoxin-induced acute lung injury. 2011

Satoshi Hagiwara, and Hideo Iwasaka, and Chihiro Shingu, and Shigekiyo Matumoto, and Akira Hasegawa, and Takayuki Noguchi
Department of Anesthesiology and Intensive Care Medicine, Oita University Faculty of Medicine, Yufu City, Oita, Japan. saku@med.oita-u.ac.jp

The incidence and prevalence of diabetes have recently increased. Hyperglycemia, which is commonly seen in intensive care medicine, is associated with increased morbidity and mortality. For instance, diabetes is associated with altered immune and hemostatic responses. High mobility group box 1 (HMGB1) protein plays a key role in various inflammatory diseases. This study investigated the increase in lung damage due to diabetes and the rise in HMGB1 levels in a lipopolysaccharide (LPS)-induced systemic inflammation rat model. Diabetes was induced by streptozotocin infusion 4 wk prior to LPS administration, followed by measurements of blood glucose and serum cytokine levels. Separate cohorts were sacrificed 12h post-LPS administration and analyzed for lung damage. Diabetic animals had significantly higher blood glucose and enhanced lung damage. In addition, levels of serum HMGB1, tumor necrosis factor-α, and interleukin-6 were increased in diabetic rats. Diabetes may exacerbate systemic inflammation as evidenced by higher serum HMGB1 and cytokine levels and enhanced lung damage in the rat systemic inflammation model.

UI MeSH Term Description Entries
D007328 Insulin A 51-amino acid pancreatic hormone that plays a major role in the regulation of glucose metabolism, directly by suppressing endogenous glucose production (GLYCOGENOLYSIS; GLUCONEOGENESIS) and indirectly by suppressing GLUCAGON secretion and LIPOLYSIS. Native insulin is a globular protein comprised of a zinc-coordinated hexamer. Each insulin monomer containing two chains, A (21 residues) and B (30 residues), linked by two disulfide bonds. Insulin is used as a drug to control insulin-dependent diabetes mellitus (DIABETES MELLITUS, TYPE 1). Iletin,Insulin A Chain,Insulin B Chain,Insulin, Regular,Novolin,Sodium Insulin,Soluble Insulin,Chain, Insulin B,Insulin, Sodium,Insulin, Soluble,Regular Insulin
D008297 Male Males
D003921 Diabetes Mellitus, Experimental Diabetes mellitus induced experimentally by administration of various diabetogenic agents or by PANCREATECTOMY. Alloxan Diabetes,Streptozocin Diabetes,Streptozotocin Diabetes,Experimental Diabetes Mellitus,Diabete, Streptozocin,Diabetes, Alloxan,Diabetes, Streptozocin,Diabetes, Streptozotocin,Streptozocin Diabete
D004195 Disease Models, Animal Naturally-occurring or experimentally-induced animal diseases with pathological processes analogous to human diseases. Animal Disease Model,Animal Disease Models,Disease Model, Animal
D004731 Endotoxins Toxins closely associated with the living cytoplasm or cell wall of certain microorganisms, which do not readily diffuse into the culture medium, but are released upon lysis of the cells. Endotoxin
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D013311 Streptozocin An antibiotic that is produced by Stretomyces achromogenes. It is used as an antineoplastic agent and to induce diabetes in experimental animals. Streptozotocin,2-Deoxy-2-((methylnitrosoamino)carbonyl)amino-D-glucose,Streptozotocine,Zanosar
D014409 Tumor Necrosis Factor-alpha Serum glycoprotein produced by activated MACROPHAGES and other mammalian MONONUCLEAR LEUKOCYTES. It has necrotizing activity against tumor cell lines and increases ability to reject tumor transplants. Also known as TNF-alpha, it is only 30% homologous to TNF-beta (LYMPHOTOXIN), but they share TNF RECEPTORS. Cachectin,TNF-alpha,Tumor Necrosis Factor Ligand Superfamily Member 2,Cachectin-Tumor Necrosis Factor,TNF Superfamily, Member 2,TNFalpha,Tumor Necrosis Factor,Cachectin Tumor Necrosis Factor,Tumor Necrosis Factor alpha
D015850 Interleukin-6 A cytokine that stimulates the growth and differentiation of B-LYMPHOCYTES and is also a growth factor for HYBRIDOMAS and plasmacytomas. It is produced by many different cells including T-LYMPHOCYTES; MONOCYTES; and FIBROBLASTS. Hepatocyte-Stimulating Factor,Hybridoma Growth Factor,IL-6,MGI-2,Myeloid Differentiation-Inducing Protein,Plasmacytoma Growth Factor,B Cell Stimulatory Factor-2,B-Cell Differentiation Factor,B-Cell Differentiation Factor-2,B-Cell Stimulatory Factor 2,B-Cell Stimulatory Factor-2,BSF-2,Differentiation Factor, B-Cell,Differentiation Factor-2, B-Cell,IFN-beta 2,IL6,Interferon beta-2,B Cell Differentiation Factor,B Cell Differentiation Factor 2,B Cell Stimulatory Factor 2,Differentiation Factor 2, B Cell,Differentiation Factor, B Cell,Differentiation-Inducing Protein, Myeloid,Growth Factor, Hybridoma,Growth Factor, Plasmacytoma,Hepatocyte Stimulating Factor,Interferon beta 2,Interleukin 6,Myeloid Differentiation Inducing Protein,beta-2, Interferon
D015897 Comorbidity The presence of co-existing or additional diseases with reference to an initial diagnosis or with reference to the index condition that is the subject of study. Comorbidity may affect the ability of affected individuals to function and also their survival; it may be used as a prognostic indicator for length of hospital stay, cost factors, and outcome or survival.

Related Publications

Satoshi Hagiwara, and Hideo Iwasaka, and Chihiro Shingu, and Shigekiyo Matumoto, and Akira Hasegawa, and Takayuki Noguchi
May 2006, Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology,
Satoshi Hagiwara, and Hideo Iwasaka, and Chihiro Shingu, and Shigekiyo Matumoto, and Akira Hasegawa, and Takayuki Noguchi
December 2004, American journal of respiratory and critical care medicine,
Satoshi Hagiwara, and Hideo Iwasaka, and Chihiro Shingu, and Shigekiyo Matumoto, and Akira Hasegawa, and Takayuki Noguchi
January 2009, Scandinavian journal of immunology,
Satoshi Hagiwara, and Hideo Iwasaka, and Chihiro Shingu, and Shigekiyo Matumoto, and Akira Hasegawa, and Takayuki Noguchi
March 2010, The British journal of nutrition,
Satoshi Hagiwara, and Hideo Iwasaka, and Chihiro Shingu, and Shigekiyo Matumoto, and Akira Hasegawa, and Takayuki Noguchi
February 2008, Shock (Augusta, Ga.),
Satoshi Hagiwara, and Hideo Iwasaka, and Chihiro Shingu, and Shigekiyo Matumoto, and Akira Hasegawa, and Takayuki Noguchi
October 2017, Acta biochimica et biophysica Sinica,
Satoshi Hagiwara, and Hideo Iwasaka, and Chihiro Shingu, and Shigekiyo Matumoto, and Akira Hasegawa, and Takayuki Noguchi
May 2009, Zhong xi yi jie he xue bao = Journal of Chinese integrative medicine,
Satoshi Hagiwara, and Hideo Iwasaka, and Chihiro Shingu, and Shigekiyo Matumoto, and Akira Hasegawa, and Takayuki Noguchi
January 2013, PloS one,
Satoshi Hagiwara, and Hideo Iwasaka, and Chihiro Shingu, and Shigekiyo Matumoto, and Akira Hasegawa, and Takayuki Noguchi
January 2015, International journal of clinical and experimental pathology,
Satoshi Hagiwara, and Hideo Iwasaka, and Chihiro Shingu, and Shigekiyo Matumoto, and Akira Hasegawa, and Takayuki Noguchi
June 2009, Zhonghua shao shang za zhi = Zhonghua shaoshang zazhi = Chinese journal of burns,
Copied contents to your clipboard!