Recombinant Rat Sodium/glucose cotransporter 1 (Slc5a1), partial

1. SGLT1 activity in lung alveolar cells of diabetic rats modulates airway surface liquid glucose concentration and bacterial proliferation. PMID: 26902517
2. CG was mainly transported into the small intestinal cells by sodium-dependent glucose transporter 1. PMID: 26658676
3. Present study indicated that inhibition of SGLT1 by phlorizin abrogated the beneficial effect of ischemic-preconditioning and for the first time, provides evidence that SGLT1 plays a crucial role in ischemic preconditioning-induced cardioprotection. PMID: 26920054
4. Elevated SGLT activity increases Na+ influx into myocytes and causes Na+ overload in type 2 diabetes. PMID: 26316524
5. Data indicate that there are several alternative channels for urea in the rat inner medulla that could potentially contribute to the high urea permeabilities in thin limb segments. PMID: 26423860
6. These findings suggest that SGLT1 in the ventromedial hypothalamus plays a significant role in the detection and activation of counterregulatory responses to hypoglycemia. PMID: 26130763
7. Chronic and direct silencing of basolateral Na-K-ATPase uniquely regulates brush border membrane Na absorptive pathways in intestinal epithelial cells. Specifically, SGLT1 is stimulated secondary to enhanced affinity of the cotransporter. PMID: 25652450
8. Immunofluorescence experiments showed that NHE3 colocalizes with SGLT2 but not SGLT1 in the renal proximal tubule. PMID: 24652792
9. Tunicamycin to inhibit glycosylation reduced SGLT1 activity. PMID: 24412219
10. Lean and obese ZDF rats exhibited disruptions in circadian feeding. Glucose intolerance was evident in lean rats, but only obese rats developed diabetes and exhibited disrupted circadian rhythmicity of SGLT1 expression and function. PMID: 23633155
11. Data suggest that contribution of Sglt1 to renal glucose reabsorption is greater under hypoglycemia than under hyperglycemia; as hypoglycemic agents, Sglt1-selective inhibitors carry a greater risk of causing hypoglycemia than Sglt2 inhibitors. PMID: 23249697
12. down regulation of the expression of SGLT1 and brush border sucrase and lactase activities may be responsible for the observed malabsorption in G. lamblia infection PMID: 22905389
13. High glucose induced cardiac myocyte p47phox translocation to the plasma membrane, resulting in SGLT1 dependent NOX2 activation. PMID: 21859816
14. SGLT1 and rosmarinic acid modulate the trafficking of SGLT1 to the brush-border membrane and may contribute to the control of plasma glucose. PMID: 21433280
15. Na/H exchange protein NHE3 and SGLT1 function together to regulate sodium absorption in the brush border membrane of intestinal epithelial cells. PMID: 21148403
16. SGLT1 glucose uptake alleviated ischemia/reperfusion-induced barrier dysfunction and bacterial translocation, partly by inhibiting epithelial apoptosis via activation of PI3K/Akt signaling. PMID: 20975661
17. the present findings show that diabetic- and/or hypertensive-induced changes in the sympathetic activity correlate with changes in SGLT1 expression in basolateral membrane of acinar cells PMID: 20841505
18. SGLT1 appears to be also expressed in alveolar type I cells PMID: 20625908
19. Infusion of sweetening agents into the small intestine resulted in rapid upregulation of sodium-glucose transporter SGLT1 in the Sprague-Dawley rat. PMID: 20395849
20. These results suggest that a short amino acid sequence of the N-terminal domain of SGLT1 plays important roles in plasma membrane targeting and specific apical localization of the protein. PMID: 11831390
21. the mechanism of absorption of quercetin-4'-glucoside involves both an interaction with SGLT1 and luminal hydrolysis by LPH, whereas quercetin-3-glucoside appears to be absorbed only following hydrolysis by LPH. PMID: 12663055
22. Age-associated decline in glucose uptake was not explained by alterations in SGLT1, GLUT2 or Na+K(+)-ATPase. PMID: 14659592
23. SGLT1 in capillaries of skeletal muscle is required for the action of insulin on D-glucose supply of myocytes PMID: 14733905
24. Food intake, rather than the light cycle, greatly affects the diurnal rhythm of SGLT1 and PEPT1 expressions. PMID: 15333706
25. Long-term hyperglycaemia leaves SGLT-1 unchanged. PMID: 15662550
26. Rapid inhibition of glucose-induced short-current circuit by leptin was associated with a parallel decrease in the abundance of sodium-glucose transporter-1 in brush border membranes. PMID: 15677491
27. in SGLT1, Cd2+ binding to the CXXC motif induces conformational changes that cause a partial inhibition of d-glucose transport PMID: 15829715
28. in the rat kidney, the expression of SGLT1 is represented by a 75-kDa protein localized largely in the PT S3 segments, where it exhibits gender differences (F > M) at both the protein and mRNA levels that are caused by androgen inhibition PMID: 16204409
29. identified GLUT-1 to -5 and SGLT-1 in the endothelial cells of cerebral, renal, and mesenteric arteries PMID: 17090404
30. Luminal leptin inhibited intestinal sugar absorption at low galactose concentrations, which indicates that leptin regulates SGLT1 activity in vivo. PMID: 17488247
31. Spermidine induction of SGLT1 in small intestine may be mediated by altered ornithine decarboxylase expression. PMID: 17673438
32. RSC1A1 codes for a 67-kDa protein named RS1 that mediates transcriptional and post-transcriptional regulation of Na(+)-D-glucose cotransporter SGLT1. PMID: 17686765
33. Indicate enterocytes are able to synthesize AngII to rapidly inhibit SGLT1-mediated glucose transport. PMID: 17702818
34. SGLT1 transcription is independent of the vagus. However, dissociation of the protein rhythm from the underlying mRNA signal by vagotomy suggests the vagus may be involved in posttranscriptional regulation of SGLT. PMID: 18308853
35. These results indicate that decreased cNO levels directly mediate the inhibition of SGLT1 and stimulation of NHE3 in intestinal epithelial cells. PMID: 18325982
36. The localization of SGLT1 in adult and prepubertal rat organs was studied using immunohistochemistry, western blotting, and RT-PCR. PMID: 18524944
37. Diurnal changes in intestinal glucose uptake capacity is linked to changes in both SGLT1 mRNA and protein. PMID: 18549898
38. The antidiabetic effect of tungstate is partly due to normalization of the activity of sucrase and SGLT1 in the brush-border membrane of enterocytes. PMID: 18617558
39. Data show that SGLT1 levels in diabetic obese rats were 1.6 folds higher than age-matched leans, respectively. PMID: 19095325
40. The persistence of SGLT1 rhythmicity in isolated loops of jejunum indicates that diurnal induction is independent of local luminal nutrient delivery, and it suggests a reliance on systemic entrainment pathways. PMID: 19231582
41. Diabetes increases SLC5A1 gene expression in salivary glands, increasing the SGLT1 protein content in the luminal membrane of ductal cells, which, by increasing water reabsorption, might explain the diabetes-induced decrease in salivary secretion. PMID: 19238474

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KEGG: rno:25552

STRING: 10116.ENSRNOP00000024165

UniGene: Rn.10224