Evidence map›Paper›PMID 36979798›Full record

ArticleBiomedicines2023

The Sympathetic Nervous System Regulates Sodium Glucose Co-Transporter 1 Expression in the Kidney.

Jennifer Matthews, Moira Hibbs, Lakshini Herat, Markus Schlaich, Vance Matthews

Open access · goldFull text read
In one paragraph

Article in Biomedicines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.6field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Jennifer MatthewsDobney Hypertension Centre, School of Biomedical Science-Royal Perth Hospital Unit, Royal Perth Hospital Research Foundation, University of Western Australia, Crawley, WA 6009, Australia.
Moira HibbsResearch Centre, Royal Perth Hospital, Perth, WA 6000, Australia.
Lakshini HeratDobney Hypertension Centre, School of Biomedical Science-Royal Perth Hospital Unit, Royal Perth Hospital Research Foundation, University of Western Australia, Crawley, WA 6009, Australia.ORCID 0000-0001-9818-006X
Markus SchlaichDobney Hypertension Centre, Medical School-Royal Perth Hospital Unit, Royal Perth Hospital Research Foundation, University of Western Australia, Crawley, WA 6009, Australia.ORCID 0000-0002-1765-0195
Vance MatthewsDobney Hypertension Centre, School of Biomedical Science-Royal Perth Hospital Unit, Royal Perth Hospital Research Foundation, University of Western Australia, Crawley, WA 6009, Australia.ORCID 0000-0001-9804-9344
The University of Western Australia · AURoyal Perth Hospital · AU

Funding

Royal Perth Hospital Research Foundation Dobney Chair (Schlaich)RPH Research Centre VMatthews2022
6 · The paper itself

Abstract

Hyperactivation of the sympathetic nervous system (SNS) has been demonstrated in various conditions including obesity, hypertension and type 2 diabetes. Elevated levels of the major neurotransmitter of the SNS, norepinephrine (NE), is a cardinal feature of these conditions. Increased levels of the sodium glucose cotransporter 1 (SGLT1) protein have been shown to occur in the parotid and submandibular glands of hypertensive rodents compared to normotensive controls. However, there was a need to examine SGLT1 expression in other tissues, such as the kidneys. Whether NE may directly affect SGLT1 protein expression has not yet been investigated, although such a link has been shown for sodium glucose cotransporter 2 (SGLT2). Hence, we aimed to determine (i) whether our murine model of neurogenic hypertension displays elevated renal SGLT1 expression and (ii) whether NE may directly promote elevations of SGLT1 in human proximal tubule (HK2) cells. We did indeed demonstrate that in vivo, in our mouse model of neurogenic hypertension, hyperactivation of the SNS promotes SGLT1 expression in the kidneys. In subsequent in vitro experiments in HK2 cells, we found that NE increased SGLT1 protein expression and translocation as assessed by both specific immunohistochemistry and/or a specific SGLT1 ELISA. Additionally, NE promoted a significant elevation in interleukin-6 (IL-6) levels which resulted in the promotion of SGLT1 expression and proliferation in HK2 cells. Our findings suggest that the SNS upregulates SGLT1 protein expression levels with potential adverse consequences for cardiometabolic control. SGLT1 inhibition may therefore provide a useful therapeutic target in conditions characterized by increased SNS activity, such as chronic kidney disease.

Indexed as

cellsdiabeteshypertensionkidneymiceSGLT1

Identifiers

PMID36979798
PMCPMC10045340
OpenAlexW4323565177

What OpenQuestion holds

Textfull text, public
LicenceCC BY
reference markers read1
measurements read30
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.