Chemistry and biology of reactive species with special reference to the antioxidative defence status in pancreatic β-cells

Diabetes mellitus is a serious metabolic disease. Dysfunction and subsequent loss of the β-cells in the islets of Langerhans through apoptosis ultimately cause a life-threatening insulin deficiency. The underlying reason for the particular vulnerability of the β-cells is an extraordinary sensitivity...

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Published inBiochimica et biophysica acta. General subjects Vol. 1861; no. 8; pp. 1929 - 1942
Main Author Lenzen, Sigurd
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.08.2017
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Abstract Diabetes mellitus is a serious metabolic disease. Dysfunction and subsequent loss of the β-cells in the islets of Langerhans through apoptosis ultimately cause a life-threatening insulin deficiency. The underlying reason for the particular vulnerability of the β-cells is an extraordinary sensitivity to the toxicity of reactive oxygen and nitrogen species (ROS and RNS) due to its low antioxidative defense status. This review considers the different aspects of the chemistry and biology of the biologically most important reactive species and their chemico-biological interactions in the β-cell toxicity of proinflammatory cytokines in type 1 diabetes and of lipotoxicity in type 2 diabetes development. The weak antioxidative defense equipment in the different subcellular organelles makes the β-cells particularly vulnerable and prone to mitochondrial, peroxisomal and ER stress. Looking upon the enzyme deficiencies which are responsible for the low antioxidative defense status of the pancreatic β-cells it is the lack of enzymatic capacity for H2O2 inactivation at all major subcellular sites. Diabetes is the most prevalent metabolic disorder with a steadily increasing incidence of both type 1 and type 2 diabetes worldwide. The weak protection of the pancreatic β-cells against oxidative stress is a major reason for their particular vulnerability. Thus, careful protection of the β-cells is required for prevention of the disease. •The β-cell is particularly vulnerable to oxidative stress due to its low antioxidative defense status.•Oxidative stress causes β-cell dysfunction in type 1 and type 2 diabetes.•Mitochondrial, peroxisomal and ER stress contribute to the diabetic metabolic state.•Mitochondria and peroxisomes are major sites of ROS generation in the β-cells.•ROS generation in the ER is important for proinsulin folding stress manifestation.
AbstractList Diabetes mellitus is a serious metabolic disease. Dysfunction and subsequent loss of the β-cells in the islets of Langerhans through apoptosis ultimately cause a life-threatening insulin deficiency. The underlying reason for the particular vulnerability of the β-cells is an extraordinary sensitivity to the toxicity of reactive oxygen and nitrogen species (ROS and RNS) due to its low antioxidative defense status. This review considers the different aspects of the chemistry and biology of the biologically most important reactive species and their chemico-biological interactions in the β-cell toxicity of proinflammatory cytokines in type 1 diabetes and of lipotoxicity in type 2 diabetes development. The weak antioxidative defense equipment in the different subcellular organelles makes the β-cells particularly vulnerable and prone to mitochondrial, peroxisomal and ER stress. Looking upon the enzyme deficiencies which are responsible for the low antioxidative defense status of the pancreatic β-cells it is the lack of enzymatic capacity for H2O2 inactivation at all major subcellular sites. Diabetes is the most prevalent metabolic disorder with a steadily increasing incidence of both type 1 and type 2 diabetes worldwide. The weak protection of the pancreatic β-cells against oxidative stress is a major reason for their particular vulnerability. Thus, careful protection of the β-cells is required for prevention of the disease. •The β-cell is particularly vulnerable to oxidative stress due to its low antioxidative defense status.•Oxidative stress causes β-cell dysfunction in type 1 and type 2 diabetes.•Mitochondrial, peroxisomal and ER stress contribute to the diabetic metabolic state.•Mitochondria and peroxisomes are major sites of ROS generation in the β-cells.•ROS generation in the ER is important for proinsulin folding stress manifestation.
Diabetes mellitus is a serious metabolic disease. Dysfunction and subsequent loss of the β-cells in the islets of Langerhans through apoptosis ultimately cause a life-threatening insulin deficiency. The underlying reason for the particular vulnerability of the β-cells is an extraordinary sensitivity to the toxicity of reactive oxygen and nitrogen species (ROS and RNS) due to its low antioxidative defense status.BACKGROUNDDiabetes mellitus is a serious metabolic disease. Dysfunction and subsequent loss of the β-cells in the islets of Langerhans through apoptosis ultimately cause a life-threatening insulin deficiency. The underlying reason for the particular vulnerability of the β-cells is an extraordinary sensitivity to the toxicity of reactive oxygen and nitrogen species (ROS and RNS) due to its low antioxidative defense status.This review considers the different aspects of the chemistry and biology of the biologically most important reactive species and their chemico-biological interactions in the β-cell toxicity of proinflammatory cytokines in type 1 diabetes and of lipotoxicity in type 2 diabetes development.SCOPE REVIEWThis review considers the different aspects of the chemistry and biology of the biologically most important reactive species and their chemico-biological interactions in the β-cell toxicity of proinflammatory cytokines in type 1 diabetes and of lipotoxicity in type 2 diabetes development.The weak antioxidative defense equipment in the different subcellular organelles makes the β-cells particularly vulnerable and prone to mitochondrial, peroxisomal and ER stress. Looking upon the enzyme deficiencies which are responsible for the low antioxidative defense status of the pancreatic β-cells it is the lack of enzymatic capacity for H2O2 inactivation at all major subcellular sites.MAJOR CONCLUSIONThe weak antioxidative defense equipment in the different subcellular organelles makes the β-cells particularly vulnerable and prone to mitochondrial, peroxisomal and ER stress. Looking upon the enzyme deficiencies which are responsible for the low antioxidative defense status of the pancreatic β-cells it is the lack of enzymatic capacity for H2O2 inactivation at all major subcellular sites.Diabetes is the most prevalent metabolic disorder with a steadily increasing incidence of both type 1 and type 2 diabetes worldwide. The weak protection of the pancreatic β-cells against oxidative stress is a major reason for their particular vulnerability. Thus, careful protection of the β-cells is required for prevention of the disease.GENERAL SIGNIFICANCEDiabetes is the most prevalent metabolic disorder with a steadily increasing incidence of both type 1 and type 2 diabetes worldwide. The weak protection of the pancreatic β-cells against oxidative stress is a major reason for their particular vulnerability. Thus, careful protection of the β-cells is required for prevention of the disease.
Diabetes mellitus is a serious metabolic disease. Dysfunction and subsequent loss of the β-cells in the islets of Langerhans through apoptosis ultimately cause a life-threatening insulin deficiency. The underlying reason for the particular vulnerability of the β-cells is an extraordinary sensitivity to the toxicity of reactive oxygen and nitrogen species (ROS and RNS) due to its low antioxidative defense status. This review considers the different aspects of the chemistry and biology of the biologically most important reactive species and their chemico-biological interactions in the β-cell toxicity of proinflammatory cytokines in type 1 diabetes and of lipotoxicity in type 2 diabetes development. The weak antioxidative defense equipment in the different subcellular organelles makes the β-cells particularly vulnerable and prone to mitochondrial, peroxisomal and ER stress. Looking upon the enzyme deficiencies which are responsible for the low antioxidative defense status of the pancreatic β-cells it is the lack of enzymatic capacity for H O inactivation at all major subcellular sites. Diabetes is the most prevalent metabolic disorder with a steadily increasing incidence of both type 1 and type 2 diabetes worldwide. The weak protection of the pancreatic β-cells against oxidative stress is a major reason for their particular vulnerability. Thus, careful protection of the β-cells is required for prevention of the disease.
Diabetes mellitus is a serious metabolic disease. Dysfunction and subsequent loss of the β-cells in the islets of Langerhans through apoptosis ultimately cause a life-threatening insulin deficiency. The underlying reason for the particular vulnerability of the β-cells is an extraordinary sensitivity to the toxicity of reactive oxygen and nitrogen species (ROS and RNS) due to its low antioxidative defense status.This review considers the different aspects of the chemistry and biology of the biologically most important reactive species and their chemico-biological interactions in the β-cell toxicity of proinflammatory cytokines in type 1 diabetes and of lipotoxicity in type 2 diabetes development.The weak antioxidative defense equipment in the different subcellular organelles makes the β-cells particularly vulnerable and prone to mitochondrial, peroxisomal and ER stress.Looking upon the enzyme deficiencies which are responsible for the low antioxidative defense status of the pancreatic β-cells it is the lack of enzymatic capacity for H2O2 inactivation at all major subcellular sites.Diabetes is the most prevalent metabolic disorder with a steadily increasing incidence of both type 1 and type 2 diabetes worldwide. The weak protection of the pancreatic β-cells against oxidative stress is a major reason for their particular vulnerability. Thus, careful protection of the β-cells is required for prevention of the disease.
Author Lenzen, Sigurd
Author_xml – sequence: 1
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  organization: Institute of Experimental Diabetes Research, Hannover Medical School, 30623 Hannover, Germany
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Issue 8
Keywords FFA
T1DM
eNOS
TNFα
Dmt1
H2O2
PBA
ERO1
RNS
UPR
Prx
CHOP
iNOS
Trx
Cytoprotective enzymes
IL-1β
ER
GPx
Fe2
NOS
NOX
nNOS
ROS
TGR
NADPH
NO
T2DM
Oxidative stress
Reactive oxygen species
O2
BiP
Grx
Pancreatic β-cells
Cytokine toxicity
Cu/ZnSOD
PDI
OH
ONOO
GSH
TrxR
GSSG
Glucolipotoxicity
SOD
FADH2
siRNA
EDTA
MnSOD
ACOXs
Diabetes
Language English
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SecondaryResourceType review_article
Snippet Diabetes mellitus is a serious metabolic disease. Dysfunction and subsequent loss of the β-cells in the islets of Langerhans through apoptosis ultimately cause...
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StartPage 1929
SubjectTerms Antioxidants - metabolism
apoptosis
chemistry
Cytokine toxicity
cytokines
Cytoprotective enzymes
Diabetes
Diabetes Mellitus - metabolism
Endoplasmic Reticulum Stress
Glucolipotoxicity
Glutathione - metabolism
Humans
hydrogen peroxide
Hydrogen Peroxide - metabolism
insulin
insulin-dependent diabetes mellitus
Insulin-Secreting Cells - metabolism
islets of Langerhans
lipotoxicity
mitochondria
nitrogen
noninsulin-dependent diabetes mellitus
Oxidative Stress
oxygen
Pancreatic β-cells
Reactive Nitrogen Species - metabolism
Reactive oxygen species
Reactive Oxygen Species - metabolism
toxicity
Title Chemistry and biology of reactive species with special reference to the antioxidative defence status in pancreatic β-cells
URI https://dx.doi.org/10.1016/j.bbagen.2017.05.013
https://www.ncbi.nlm.nih.gov/pubmed/28527893
https://www.proquest.com/docview/1901310017
https://www.proquest.com/docview/2000456295
Volume 1861
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