Thiosulfate sulfurtransferase prevents hyperglycemic damage to the zebrafish pronephros in an experimental model for diabetes
0301 basic medicine
Type 2/metabolism
Science
Thiosulfates
Article
Pronephros
03 medical and health sciences
Theoretical
Models
Zebrafish/metabolism
Diabetes Mellitus
Animals
Zebrafish
2. Zero hunger
Q
R
Pronephros/metabolism
Models, Theoretical
Hyperglycemia/complications
Thiosulfate Sulfurtransferase
Thiosulfate Sulfurtransferase/metabolism
3. Good health
Diabetes Mellitus, Type 2
Hyperglycemia
Medicine
DOI:
10.1038/s41598-022-16320-1
Publication Date:
2022-07-15T10:04:11Z
AUTHORS (13)
ABSTRACT
AbstractThiosulfate sulfurtransferase (TST, EC 2.8.1.1), also known as Rhodanese, was initially discovered as a cyanide detoxification enzyme. However, it was recently also found to be a genetic predictor of resistance to obesity-related type 2 diabetes. Diabetes type 2 is characterized by progressive loss of adequate β-cell insulin secretion and onset of insulin resistance with increased insulin demand, which contributes to the development of hyperglycemia. Diabetic complications have been replicated in adult hyperglycemic zebrafish, including retinopathy, nephropathy, impaired wound healing, metabolic memory, and sensory axonal degeneration. Pancreatic and duodenal homeobox 1 (Pdx1) is a key component in pancreas development and mature beta cell function and survival. Pdx1 knockdown or knockout in zebrafish induces hyperglycemia and is accompanied by organ alterations similar to clinical diabetic retinopathy and diabetic nephropathy. Here we show that pdx1-knockdown zebrafish embryos and larvae survived after incubation with thiosulfate and no obvious morphological alterations were observed. Importantly, incubation with hTST and thiosulfate rescued the hyperglycemic phenotype in pdx1-knockdown zebrafish pronephros. Activation of the mitochondrial TST pathway might be a promising option for therapeutic intervention in diabetes and its organ complications.
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CITATIONS (5)
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