2015
DOI: 10.1016/j.imlet.2014.12.006
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Immunotoxicological effects of streptozotocin and alloxan: In vitro and in vivo studies

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Cited by 23 publications
(27 citation statements)
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“…It has been reported that supplementation of fish oil can prevent the development of alloxan-induced diabetes mellitus in experimental animals. 40 HbA1c reflects a large amount of blood glucose attached to hemoglobin in red blood cells to form glycosylated hemoglobin, and thus is an important factor to monitor long-term blood glucose balance. The effects of individual polyunsaturated fatty acids on preventing alloxan induced diabetes mellitus in experimental animals were studied.…”
Section: Discussionmentioning
confidence: 99%
“…It has been reported that supplementation of fish oil can prevent the development of alloxan-induced diabetes mellitus in experimental animals. 40 HbA1c reflects a large amount of blood glucose attached to hemoglobin in red blood cells to form glycosylated hemoglobin, and thus is an important factor to monitor long-term blood glucose balance. The effects of individual polyunsaturated fatty acids on preventing alloxan induced diabetes mellitus in experimental animals were studied.…”
Section: Discussionmentioning
confidence: 99%
“…b). GLUT2 is further expressed in the kidney and liver; known side effects in this model include kidney and liver damage, reduced animal body weight, and increased risk of developing tumors . STZ also affects the immune system, leading to early lymphopenia in vitro and in vivo with an unexpected toxicity against CD8 T cells and B cells.…”
Section: Autoimmune‐component In Type 1 Diabetes In Humans In Nonobementioning
confidence: 99%
“…These properties of STZ may even exert a protective effect against the onset of diabetes in young NOD mice, potentially by inducing a regulatory T‐cell population . Further, since STZ exhibits immunosuppressive effects, islet grafts may survive longer in STZ‐induced diabetic mice compared with mice injected with other diabetes‐inducing drugs . STZ‐induced diabetic mice represent an economic strategy to induce diabetes, since the maintenance of NOD mice under SPF conditions is associated with relatively high costs.…”
Section: Autoimmune‐component In Type 1 Diabetes In Humans In Nonobementioning
confidence: 99%
“…Streptozotocin (STZ) (2-deoxy-2-(3-(methyl-3-nitrosoureido)-D-glucopyranose) is a nitrosourea compound that targets beta cells by entering via the glucose transporter, GLUT2, and is a widely used drug for inducing T1DM by inducing stress and DNA alkylation (cleaving) leading to cellular apoptosis [65,66]. STZ can either be administered intraperitoneally at a low dose (40-60 mg/g in 0.1M citrate buffer) continuously for 5 days or at a single high dosage (100-200 mg/kg), though the osteoporosis phenotype is dosage dependent [64].…”
Section: Type 1 Diabetic Mellitus Animal Modelsmentioning
confidence: 99%