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唾液腺导管细胞中 SGLT1 表达的增加与糖尿病和高血压大鼠的低分泌有关。

Increased SGLT1 expression in salivary gland ductal cells correlates with hyposalivation in diabetic and hypertensive rats.

机构信息

Universidade Federal de Uberlândia, Instituto de Ciências Biomédicas - Área de Fisiologia e Farmacologia Av, Pará, 1720 Campus Umuruama, CEP: 38400-902 Uberlândia-MG, Brazil.

出版信息

Diabetol Metab Syndr. 2013 Oct 24;5(1):64. doi: 10.1186/1758-5996-5-64.

DOI:10.1186/1758-5996-5-64
PMID:24499577
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4029169/
Abstract

BACKGROUND

Oral health complications in diabetes and hypertension include decreased salivary secretion. The sodium-glucose cotransporter 1 (SGLT1) protein, which transports 1 glucose/2 Na+/264 H2O molecules, is described in salivary glands. We hypothesized that changes in SGLT1 expression in the luminal membrane of ductal cell may be related to an altered salivary flow.

FINDINGS

By immunohistochemistry, we investigated SGLT1 expression in ductal cells of parotid and submandibular glands from Wistar Kyoto rats (WKY), diabetic WKY (WKY-D), spontaneously hypertensive rats (SHR) and diabetic SHR (SHR-D), as well as in parotid glands from WKY subjected to sympathetic stimulation, with or without previous propranolol blockade. Diabetes and hypertension decreased the salivary secretion and increased SGLT1 expression in the luminal membrane of ductal cells, and their association exacerbated the regulations observed. After 30 min of sympathetic stimulation, SGLT1 increased in the luminal membrane of ductal cells, and that was blocked by previous injection of propranolol.

CONCLUSIONS

SGLT1 expression increases in the luminal membrane of salivary gland ductal cells and the salivary flow decreases in diabetic and hypertensive rats, which may be related to sympathetic activity. This study highlights the water transporter role of SGLT1 in salivary glands, which, by increasing ductal water reabsorption, may explain the hyposalivation of diabetic and hypertensive subjects.

摘要

背景

糖尿病和高血压的口腔健康并发症包括唾液分泌减少。钠-葡萄糖共转运蛋白 1(SGLT1)蛋白在唾液腺中被描述为转运 1 个葡萄糖/2 个 Na+/264 个 H2O 分子。我们假设,导管细胞腔膜中 SGLT1 表达的变化可能与唾液流量的改变有关。

发现

通过免疫组织化学,我们研究了 Wistar Kyoto 大鼠(WKY)、糖尿病 Wistar Kyoto 大鼠(WKY-D)、自发性高血压大鼠(SHR)和糖尿病自发性高血压大鼠(SHR-D)腮腺和颌下腺导管细胞中 SGLT1 的表达,以及交感神经刺激后的 WKY 腮腺中 SGLT1 的表达,同时或不预先注射普萘洛尔阻断。糖尿病和高血压降低了唾液分泌量,并增加了导管细胞腔膜中的 SGLT1 表达,其相关性加剧了观察到的调节。在交感神经刺激 30 分钟后,导管细胞腔膜中的 SGLT1 增加,而这一增加被先前注射普萘洛尔所阻断。

结论

糖尿病和高血压大鼠唾液腺导管细胞腔膜中的 SGLT1 表达增加,唾液流量减少,这可能与交感神经活动有关。本研究强调了 SGLT1 在唾液腺中的水转运蛋白作用,通过增加导管水重吸收,可能解释了糖尿病和高血压患者的唾液减少。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb76/4029169/8c7cb4539cfa/1758-5996-5-64-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb76/4029169/8c7cb4539cfa/1758-5996-5-64-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb76/4029169/8c7cb4539cfa/1758-5996-5-64-1.jpg

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本文引用的文献

1
Biology of human sodium glucose transporters.人类钠-葡萄糖转运体的生物学特性。
Physiol Rev. 2011 Apr;91(2):733-94. doi: 10.1152/physrev.00055.2009.
2
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Am J Physiol Endocrinol Metab. 2010 Dec;299(6):E1028-37. doi: 10.1152/ajpendo.00395.2010. Epub 2010 Sep 14.
3
SLC2A2 gene expression in kidney of diabetic rats is regulated by HNF-1alpha and HNF-3beta.
挖掘唾液的诊断潜力:红外光谱及其在唾液分析中的应用综述
J Pers Med. 2023 May 28;13(6):907. doi: 10.3390/jpm13060907.
4
Major depression-related factor NEGR1 controls salivary secretion in mouse submandibular glands.与重度抑郁症相关的因子NEGR1控制小鼠下颌下腺的唾液分泌。
iScience. 2023 Apr 26;26(5):106773. doi: 10.1016/j.isci.2023.106773. eCollection 2023 May 19.
5
Salivary ATR-FTIR Spectroscopy Coupled with Support Vector Machine Classification for Screening of Type 2 Diabetes Mellitus.唾液衰减全反射傅里叶变换红外光谱结合支持向量机分类用于2型糖尿病筛查
Diagnostics (Basel). 2023 Apr 12;13(8):1396. doi: 10.3390/diagnostics13081396.
6
Oral health and diabetes.口腔健康与糖尿病。
Natl J Maxillofac Surg. 2022 Sep-Dec;13(3):319-321. doi: 10.4103/njms.njms_197_22. Epub 2022 Dec 10.
7
Association of salivary alpha-2-macroglobulin with glycemia and glycated hemoglobin in type 2 diabetes mellitus: a systematic review and meta-analysis study.唾液α-2-巨球蛋白与 2 型糖尿病患者血糖和糖化血红蛋白的相关性:系统评价和荟萃分析研究。
Sao Paulo Med J. 2022 Nov-Dec;140(6):818-828. doi: 10.1590/1516-3180.2021.0816.R2.19052022.
8
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9
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10
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PLoS One. 2020 Mar 17;15(3):e0223461. doi: 10.1371/journal.pone.0223461. eCollection 2020.
糖尿病大鼠肾脏中SLC2A2基因的表达受肝细胞核因子-1α(HNF-1α)和肝细胞核因子-3β(HNF-3β)调控。
Mol Cell Endocrinol. 2009 Jun 16;305(1-2):63-70. doi: 10.1016/j.mce.2009.02.014. Epub 2009 Mar 4.
4
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J Membr Biol. 2009 Mar;228(2):63-9. doi: 10.1007/s00232-009-9159-3. Epub 2009 Feb 24.
5
Revised immunolocalization of the Na+-D-glucose cotransporter SGLT1 in rat organs with an improved antibody.利用改良抗体对大鼠器官中钠-葡萄糖共转运蛋白SGLT1进行的免疫定位研究
Am J Physiol Cell Physiol. 2008 Aug;295(2):C475-89. doi: 10.1152/ajpcell.00180.2008. Epub 2008 Jun 4.
6
T1R3 and gustducin in gut sense sugars to regulate expression of Na+-glucose cotransporter 1.肠道中的味觉受体1型成员3(T1R3)和味觉传导素感知糖类,以调节钠-葡萄糖协同转运蛋白1的表达。
Proc Natl Acad Sci U S A. 2007 Sep 18;104(38):15075-80. doi: 10.1073/pnas.0706678104. Epub 2007 Aug 27.
7
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Am J Physiol Gastrointest Liver Physiol. 2004 Jul;287(1):G151-61. doi: 10.1152/ajpgi.00480.2003. Epub 2004 Feb 26.
8
Excretion of sodium, potassium, chloride and carbon dioxide in human parotid saliva.人体腮腺唾液中钠、钾、氯和二氧化碳的排泄
Am J Physiol. 1954 Jul;178(1):155-9. doi: 10.1152/ajplegacy.1954.178.1.155.
9
Glucose sensing in the intestinal epithelium.肠道上皮中的葡萄糖感知
Eur J Biochem. 2003 Aug;270(16):3377-88. doi: 10.1046/j.1432-1033.2003.03721.x.
10
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J Physiol. 2002 Jul 1;542(Pt 1):53-60. doi: 10.1113/jphysiol.2002.018713.