Evidence map›Paper›PMID 17679035›Full record

ArticleAmerican journal of hypertension2007

Therapeutic actions of allylmercaptocaptopril and captopril in a rat model of metabolic syndrome.

Paul Ernsberger, Janean L Johnson, Talma Rosenthal, David Mirelman, Richard J Koletsky

Open access · bronzeAbstract read
In one paragraph

Article in American journal of hypertension, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.6field-weighted citation impact, top 6% 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

15 citing papers in PubMed, 34 citations in OpenAlex.

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  7. Elevated Urinary T Helper 1 Chemokine Levels in Newly Diagnosed Hypertensive Obese Children.Journal of clinical research in pediatric endocrinology · 2015
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  15. The metabolic syndrome.Endocrine reviews · 2008
    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 3 institutions in 2 countries.

Paul ErnsbergerDepartment of Nutrition, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106-4906, USA. pre@po.cwru.edu
Janean L Johnson
Talma Rosenthal
David Mirelman
Richard J Koletsky
Case Western Reserve University · USTel Aviv University · ILWeizmann Institute of Science · IL

Funding

NEURONAL IMIDAZOLINE RECEPTORS IN CARDIOVASCULAR CONTROLR01HL044514 · NHLBI · CASE WESTERN RESERVE UNIVERSITY · PI ERNSBERGER, PAUL R · 1997 to 2004
$1.1M
NHLBI NIH HHS R01 HL044514
6 · The paper itself

Abstract

backgroundHypertension often coexists with hyperlipidemia, insulin resistance, and glucose intolerance in metabolic syndrome. Allylmercaptocaptopril is a conjugate of the angiotensin-converting enzyme inhibitor captopril with allicin, an active principle in garlic with multiple beneficial actions on metabolic-syndrome abnormalities. We sought to test the hypothesis that the conjugation of allicin to captopril may confer additional therapeutic actions in metabolic disease.

methodsWe compared allylmercaptocaptopril (53.5 mg/kg/day orally for 60 days) to an equimolar dose of captopril (40 mg/kg/day) in the spontaneously hypertensive, obese rat (SHROB) model.

resultsAllylmercaptocaptopril prevented progressive weight gain, without a detectable effect on food intake. Both captopril and allylmercaptocaptopril lowered blood pressure, but allylmercaptocaptopril was more effective. Allylmercaptocaptopril, but not captopril, improved cardiac hypertrophy, as indicated by heart weight and ventricular-wall thickness. Allylmercaptocaptopril improved, whereas captopril impaired, oral glucose tolerance after a fast. Triglycerides were decreased by both captopril and allylmercaptocaptopril. Total cholesterol and non-HDL cholesterol were reduced by captopril but not by allylmercaptocaptopril. The SHROB rats developed severe glomerulosclerosis and renal failure. Allylmercaptocaptopril showed significant nephro-protection, as indicated by reductions in urinary protein loss, urinary protein-to-creatinine ratio, and plasma creatinine. Captopril showed the same trends and also prevented the decline of creatinine clearance. Finally, both allylmercaptocaptopril and captopril reduced the basal level of lipolysis in isolated abdominal adipocytes, and restored the response to catecholamine stimulation.

conclusionsBoth captopril and allylmercaptocaptopril are effective in attenuating multiple abnormalities of metabolic syndrome. Allylmercaptocaptopril may have additional effectiveness on improving glucose tolerance, further lowering blood pressure, reducing cardiac hypertrophy, preventing weight gain, and protecting against renal disease.

Indexed as

Administration, OralAngiotensin-Converting Enzyme InhibitorsAnimalsBlood GlucoseBlood PressureCaptoprilDisease Models, AnimalDisulfidesDose-Response Relationship, DrugDrug CombinationsFemaleHypoglycemic AgentsInsulinMaleMetabolic SyndromeRatsallicinAngiotensin-Converting Enzyme InhibitorsBlood GlucoseCaptoprilDisulfidesDrug CombinationsHypoglycemic AgentsInsulinSulfinic Acids

Identifiers

PMID17679035
PMCPMC2930912
OpenAlexW2062744722

What OpenQuestion holds

Textmetadata
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.