Improved diabetic syndrome in C57BL/KsJ-db/db mice by oral administration of the Na(+)-glucose cotransporter inhibitor T-1095
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Thioglycosides as inhibitors of hSGLT1 and hSGLT2: potential therapeutic agents for the control of hyperglycemia in diabetesRenal sodium glucose cotransporter 2 inhibitors as a novel therapeutic approach to treatment of type 2 diabetes: Clinical data and mechanism of actionRodent models of diabetic nephropathy: their utility and limitationsThe Na(+)/glucose cotransporters: from genes to therapyEffect of canagliflozin on renal threshold for glucose, glycemia, and body weight in normal and diabetic animal modelsMetabolomics reveals attenuation of the SLC6A20 kidney transporter in nonhuman primate and mouse models of type 2 diabetes mellitusDevelopment and potential role of type-2 sodium-glucose transporter inhibitors for management of type 2 diabetes.Beneficial effects of canagliflozin in combination with pioglitazone on insulin sensitivity in rodent models of obese type 2 diabetes.Comprehensive evidence-based assessment and prioritization of potential antidiabetic medicinal plants: a case study from canadian eastern james bay cree traditional medicineRenal hyperfiltration related to diabetes mellitus and obesity in human disease.Proinsulin maturation, misfolding, and proteotoxicity.LX4211, a dual SGLT1/SGLT2 inhibitor, improved glycemic control in patients with type 2 diabetes in a randomized, placebo-controlled trial.Renal sodium-glucose cotransporter inhibition in the management of type 2 diabetes mellitusSodium-glucose cotransporter inhibition prevents oxidative stress in the kidney of diabetic rats.SHR3824, a novel selective inhibitor of renal sodium glucose cotransporter 2, exhibits antidiabetic efficacy in rodent models.Effects of phlorizin on diabetic retinopathy according to isobaric tags for relative and absolute quantification-based proteomics in db/db mice.Exercise-like effects by Estrogen-related receptor-gamma in muscle do not prevent insulin resistance in db/db mice.Advances in murine models of diabetic nephropathy.Tofogliflozin, a novel sodium-glucose co-transporter 2 inhibitor, improves renal and pancreatic function in db/db mice.Tofogliflozin, a sodium/glucose cotransporter 2 inhibitor, attenuates body weight gain and fat accumulation in diabetic and obese animal models.A review of rodent models of type 2 diabetic skeletal fragility.Sodium-glucose transport: role in diabetes mellitus and potential clinical implications.SGLT2 inhibitors: a new emerging therapeutic class in the treatment of type 2 diabetes mellitus.Pathophysiology of the diabetic kidney.The kidney as a new target for antidiabetic drugs: SGLT2 inhibitors.Lowering plasma glucose concentration by inhibiting renal sodium-glucose cotransport.How the kidney hyperfiltrates in diabetes: From molecules to hemodynamics.SGLT2 Inhibitors as a Therapeutic Option for Diabetic Nephropathy.Accumulation of worn-out GBM material substantially contributes to mesangial matrix expansion in diabetic nephropathy.miR-21 is a key therapeutic target for renal injury in a mouse model of type 2 diabetes.Acute SGLT inhibition normalizes O2 tension in the renal cortex but causes hypoxia in the renal medulla in anaesthetized control and diabetic rats.Glycemic Control with Ipragliflozin, a Novel Selective SGLT2 Inhibitor, Ameliorated Endothelial Dysfunction in Streptozotocin-Induced Diabetic MouseGlycemic control with empagliflozin, a novel selective SGLT2 inhibitor, ameliorates cardiovascular injury and cognitive dysfunction in obese and type 2 diabetic mice.SGLT2 deletion improves glucose homeostasis and preserves pancreatic beta-cell function5-(4-Ethoxy-benzyl)-1H-tetra-zoleInhibition of SGLT2 alleviates diabetic nephropathy by suppressing high glucose-induced oxidative stress in type 1 diabetic miceReduced renal sympathetic nerve activity contributes to elevated glycosuria and improved glucose tolerance in hypothalamus-specific Pomc knockout miceRenal glucose handling in diabetes and sodium glucose cotransporter 2 inhibition.Mapping murine diabetic kidney disease using chemical exchange saturation transfer MRI.Green tea extract with polyethylene glycol-3350 reduces body weight and improves glucose tolerance in db/db and high-fat diet mice.
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P2860
Improved diabetic syndrome in C57BL/KsJ-db/db mice by oral administration of the Na(+)-glucose cotransporter inhibitor T-1095
description
2001 nî lūn-bûn
@nan
2001 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Improved diabetic syndrome in ...... cotransporter inhibitor T-1095
@ast
Improved diabetic syndrome in ...... cotransporter inhibitor T-1095
@en
Improved diabetic syndrome in ...... cotransporter inhibitor T-1095
@nl
type
label
Improved diabetic syndrome in ...... cotransporter inhibitor T-1095
@ast
Improved diabetic syndrome in ...... cotransporter inhibitor T-1095
@en
Improved diabetic syndrome in ...... cotransporter inhibitor T-1095
@nl
prefLabel
Improved diabetic syndrome in ...... cotransporter inhibitor T-1095
@ast
Improved diabetic syndrome in ...... cotransporter inhibitor T-1095
@en
Improved diabetic syndrome in ...... cotransporter inhibitor T-1095
@nl
P2093
P2860
P3181
P356
P1476
Improved diabetic syndrome in ...... cotransporter inhibitor T-1095
@en
P2093
K Kitamura
M Matsumoto
T Ishihara
P2860
P304
P3181
P356
10.1038/SJ.BJP.0703829
P407
P577
2001-01-01T00:00:00Z