Evidence map›Paper›PMID 26818652›Full record

ArticleHypertension research : official journal of the Japanese Society of Hypertension2016

A sodium-glucose co-transporter 2 inhibitor empagliflozin prevents abnormality of circadian rhythm of blood pressure in salt-treated obese rats.

Yui Takeshige, Yoshihide Fujisawa, Asadur Rahman, Wararat Kittikulsuth, Daisuke Nakano, Hirohito Mori, Tsutomu Masaki, Koji Ohmori, Masakazu Kohno, Hiroaki Ogata and 1 more

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In one paragraph

Article in Hypertension research : official journal of the Japanese Society of Hypertension, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
6.4field-weighted citation impact, top 3% 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

34 citing papers in PubMed, 58 citations in OpenAlex.

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  13. SGLT2 inhibition effect on salt-induced hypertension, RAAS, and NaAmerican journal of physiology. Renal physiology · 2022
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  17. Molecular Mechanisms of SGLT2 Inhibitor on Cardiorenal Protection.International journal of molecular sciences · 2020
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Yui TakeshigeDepartment of Pharmacology, Faculty of Medicine, Kagawa University, Kagawa, Japan.
Yoshihide FujisawaLife Science Research Center, Faculty of Medicine, Kagawa University, Kagawa, Japan.
Asadur RahmanDepartment of Pharmacology, Faculty of Medicine, Kagawa University, Kagawa, Japan.
Wararat KittikulsuthDepartment of Pharmacology, Faculty of Medicine, Kagawa University, Kagawa, Japan.
Daisuke NakanoDepartment of Pharmacology, Faculty of Medicine, Kagawa University, Kagawa, Japan.
Hirohito MoriDepartment of Gastroenterology, Faculty of Medicine, Kagawa University, Kagawa, Japan.
Tsutomu MasakiDepartment of Gastroenterology, Faculty of Medicine, Kagawa University, Kagawa, Japan.
Koji OhmoriDepartment of Cardiology, Faculty of Medicine, Kagawa University, Kagawa, Japan.
Masakazu KohnoDepartment of Cardiology, Faculty of Medicine, Kagawa University, Kagawa, Japan.
Hiroaki OgataDivision of Nephrology, Department of Medicine, Showa University School of Medicine, Yokohama, Japan.
Akira NishiyamaDepartment of Pharmacology, Faculty of Medicine, Kagawa University, Kagawa, Japan.
Kagawa University · JPShowa University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Studies were performed to examine the effects of the selective sodium-glucose co-transporter 2 (SGLT2) inhibitor empagliflozin on urinary sodium excretion and circadian blood pressure in salt-treated obese Otsuka Long Evans Tokushima Fatty (OLETF) rats. Fifteen-week-old obese OLETF rats were treated with 1% NaCl (in drinking water), and vehicle (0.5% carboxymethylcellulose, n=10) or empagliflozin (10 mg kg(-1)per day, p.o., n=11) for 5 weeks. Blood pressure was continuously measured by telemetry system. Glucose metabolism and urinary sodium excretion were evaluated by oral glucose tolerance test and high salt challenge test, respectively. Vehicle-treated OLETF rats developed non-dipper type blood pressure elevation with glucose intolerance and insulin resistance. Compared with vehicle-treated animals, empagliflozin-treated OLETF rats showed an approximately 1000-fold increase in urinary glucose excretion and improved glucose metabolism and insulin resistance. Furthermore, empagliflozin prevented the development of blood pressure elevation with normalization of its circadian rhythm to a dipper profile, which was associated with increased urinary sodium excretion. These data suggest that empagliflozin elicits beneficial effects on both glucose homeostasis and hypertension in salt-replete obese states.

Indexed as

Sodium-Glucose Transporter 2 InhibitorsAnimalsBenzhydryl CompoundsBlood GlucoseBlood PressureCircadian RhythmGlucose Tolerance TestGlucosidesHomeostasisHypertensionHypoglycemic AgentsInsulin ResistanceObesityRatsRats, Inbred OLETFSodium Chloride, DietaryBenzhydryl CompoundsBlood GlucoseempagliflozinGlucosidesHypoglycemic AgentsSlc5a2 protein, mouseSodium Chloride, DietarySodium-Glucose Transporter 2Sodium-Glucose Transporter 2 Inhibitors

Identifiers

PMID26818652
OpenAlexW2342735140

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.