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PHBio#10 Diabetes

QuestionAnswer
adult-onset diabetes Type II diabetes
advanced glycosylation end products (AGE) abnormally-shaped, dysfunctional structural molecules of the body formed when glucose irreversibly binds to fat, protein, or nucleic acids as a result of chronic hyperglycemia
concordance phenotypic similarity in twins
creatinine a metabolic waste product produced by the breakdown of muscle protein
diabetes a group of metabolic diseases characterized by persistently elevated blood glucose levels and associated abnormalities in lipid and protein metabolism
euglycemia normal blood glucose levels
glomeruli the filtering tissue of the kidneys composed of loops of capillaries that lie adjacent to the excretory ducts that connect to the ureters and bladder
glycosylation nonenzymatic binding of glucose to other molecules such as proteins, fats, or nucleic acids
hyperglycemia elevated level of blood glucose
hypoalbuminemia abnormally low levels of albumin in blood
insulin a protein hormone produced by the beta cells of the pancreas that regulates glucose levels in the body
insulin dependent diabetes mellitus (IDDM) Type I diabetes
insulin resistance unresponsiveness of cells to the effect of insulin, reducing their ability to absorb glucose, resulting in hyperglycemia
juvenile diabetes Type I diabetes
lipidurea excretion of lipid in urine
MAP (mitogen-activated protein) kinase pathway a cell signaling system that phosphorylates molecules and is associated with tissue remodeling
metabolic syndrome a cluster of metabolic abnormalities defined as any combination of three of the following: abdominal obesity, glucose intolerance, hypertension, and abnormal blood lipid levels
microalbuminurea the excretion of small but abnormal amounts of albumin, the primary protein within the serum of the circulatory system, into the urine often associated with early kidney damage
nephrotic syndrome a combination of abnormal conditions associated with advanced renal disease consisting of hypoalbuminemia, proteinurea, edema, hyperlipidemia, and lipidurea
nephropathy kidney disease
Non-insulin dependent diabetes mellitus (NIDDM) Type II diabetes
pancreatic beta cells the cells of the pancreas that produce, store, and release insulin into the bloodstream, thereby regulating blood glucose levels
peroxisome proliferator-activated receptors (PPARs) a group of receptor molecules within the cell nucleus that activate transcription of genes that regulate the breakdown and storage of fat
polydipsia excessive thirst
polyphagia excessive appetite
polyurea frequent urination
proteinurea excretion of large amounts of protein in the urine, often, but not always associated with established kidney disease
thiazoladinediones a group of pharmacological agents that increase sensitivity of peripheral tissues to insulin-mediated glucose uptake
Type I diabetes diabetes that results from destruction of the pancreatic beta cells causing inability to produce insulin
Type II diabetes diabetes caused by either insufficient insulin production by pancreatic beta cells or peripheral insulin resistance
urea a metabolic waste product produced by the breakdown of protein
Created by: gasiorr
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