Evidence map›Paper›PMID 40893718›Full record

ArticleARYA atherosclerosis2025

The mechanism of vascular adhesion molecule-1 in an ischemia-reperfusion cardia model.

Seyedamirhossein Zarei, Afshin Nazari, Farzaneh Chehelcheraghi, Mehdi Birjandi, Roxana Karbaschi

Abstract read
In one paragraph

Article in ARYA atherosclerosis, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Seyedamirhossein ZareiStudent Research Committee, School of Medicine, Lorestan University of Medical Sciences, Khorramabad, Iran.
Afshin NazariDepartment of Physiology and Pharmacology, School of Medicine, Cardiovascular Research Center, Lorestan University of Medical Sciences, Khorramabad, Lorestan, Iran.
Farzaneh ChehelcheraghiGastroenterology and Liver Diseases Research Center, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Mehdi BirjandiDepartment of Nutritional Health Research Center, School of Health and Nutrition, Lorestan University of Medical Sciences, Khorramabad, Iran.
Roxana KarbaschiFaculty of Nursing and Midwifery, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundVascular adhesion molecule-1 (VCAM-1) is involved in promoting inflammation within blood vessels, activating endothelial cells, and is a key factor in the progression of diabetic vasculopathy in rats with diabetes, contributing to the underlying pathophysiological processes. This study focused on the expression level of VCAM-1 in diabetic rats subjected to a six-week schedule of aerobic training and valerian supplements.

methodsFifty male Wistar rats' hearts were removed under deep anesthesia and were studied using Lutgendorf's apparatus. They were divided into five groups (10 each): Healthy control (C), Diabetic control (DC), Diabetic with valerian (DV), Diabetic with exercise (DE), and Diabetic with valerian and exercise (DVE). Diabetes was induced in the animals by administering a shot of STZ (50 mg/kg) in their abdominal area. Following confirmation of diabetes in the animals, moderate exercise five days a week, combined with intraperitoneal administration of 200 mg/kg/day of valerian, was maintained for six weeks. Heart tissue was obtained from diabetic cardiac ischemia-reperfusion model (CI/RM) injury (n=40) and control rats (n=10).

resultsVCAM-1 expression and histological parameters were not observed when comparing experimental and control groups. However, the exercise/valerian treatment (E + V) notably reduced the irregularity in cardiac tissue and increased the size of cardiomyocytes.

conclusionThese findings suggest that E + V extract could diminish the levels of diabetic cardiac complications. Also, it had a dual effect: it corrected cardiac tissue abnormalities and increased the size of cardiomyocytes, enhancing the overall structure and function of the heart. More research is needed to understand non-pharmacological complementary treatments in this area.

Indexed as

Cardiac Rats; Diabetic VasculopathyCardiomyocytesDiabetes MellitusEndothelial CellsMyocardial IschemiaValerianVascular Cell Adhesion Molecule-1

Identifiers

PMID40893718
PMCPMC12398703

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