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A key chemical triggers powerful muscle movements in the esophagus and stomach: new clues to digestive reactions and allergies

Researchers discovered that platelet-activating factor (PAF) triggers strong contractions in the esophagus and upper stomach, potentially linked to food allergies and acid reflux. PAF also causes rhythmic muscle movements in the colon, which may be connected to chronic digestive diseases.

SourceToho University·JournalBiological and Pharmaceutical Bulletin·TypeExperimental study·DateMay 20, 2025

Circulation: A new mechanism of early-onset atherosclerosis in a premature aging syndrome

Researchers at CNIC have identified endothelial-to-mesenchymal transition as a novel mechanism in premature atherosclerosis in progeria. The study proposes a new therapeutic target for this disease and highlights the importance of investigating rare diseases like progeria.

SourceCentro Nacional de Investigaciones Cardiovasculares Carlos III (F.S.P.)·JournalCirculation·TypeExperimental study·DateSep 10, 2024

New approach to the design of therapies that enhance the effect of cholesterol-lowering drugs

Researchers discovered that reducing cholesterol levels in mice with advanced atherosclerosis leads to a decrease in the number of smooth muscle-derived cells causing plaque growth, while preserving stabilizing cell types. This finding opens up new opportunities for targeted therapies.

SourceCentro Nacional de Investigaciones Cardiovasculares Carlos III (F.S.P.)·JournalNature Cardiovascular Research·TypeExperimental study·DateFeb 1, 2024

Researchers uncover why a gene mutant causes young children to have strokes

Researchers discovered that a mutation in the gene ACTA2 causes moyamoya disease and strokes in young children. The mutation leads to dysfunctional smooth muscle cells in arteries, resulting in blockages and increased risk of stroke. Understanding this mechanism could lead to new treatments for moyamoya disease.

SourceUniversity of Texas Health Science Center at Houston·JournalNature Cardiovascular Research·DateSep 28, 2023

Researchers uncover how a genetic mutation can cause individuals with normal cholesterol levels to develop coronary artery disease at a young age

A novel molecular pathway has been identified, explaining how a mutation in the ACTA2 gene can cause individuals in their 30s with normal cholesterol levels to develop coronary artery disease. The mutation leads to stress in smooth muscle cells, triggering the production of excess cholesterol and driving atherosclerotic plaque formation.

SourceUniversity of Texas Health Science Center at Houston·JournalEuropean Heart Journal·DateJul 7, 2023

A Mass General team is the first to trace a rare smooth muscle disorder to a single mutation in a non-coding gene

A Mass General team has identified a single mutation in a non-coding gene, MIR145-5p, as the source of multisystemic smooth muscle dysfunction syndrome, which had gone undiagnosed in a child for years. The discovery enabled physicians to initiate treatment and lessen the risk of future strokes.

SourceMassachusetts General Hospital·JournalJournal of Clinical Investigation·DateFeb 28, 2023

α-Ketoglutarate (AKG) as a nutritional supplement to enhance health and exercise performance

Research reveals that α-Ketoglutarate (AKG) supplementation promotes skeletal muscle mass, improves exercise endurance, and increases blood flow, making it a potential nutritional supplement for enhancing health and exercise performance. AKG also relaxes vascular smooth muscle, allowing tissues to receive abundant oxygen and nutrients.

SourceHigher Education Press·JournalLife Metabolism·TypeExperimental study·DateOct 24, 2022

Biased beta-agonists may provide better control of asthma and other obstructive lung diseases, drug discovery study shows

A University of South Florida Health-led team discovered a lead candidate that selectively relaxes airway smooth muscle cells with no detectable drug desensitization. The biased beta-agonist, C1-S, offers a therapeutic option for asthma and obstructive lung diseases without the rapid loss of effectiveness seen with traditional β-agonists.

SourceUniversity of South Florida (USF Health)·JournalProceedings of the National Academy of Sciences·TypeExperimental study·DateNov 22, 2021

Young innovators

Day's research develops layer-by-layer assembled nanoshells to deliver tumor suppressor miR-34a into cells, reducing cancer cell growth. Gleghorn discovers TRPV4 regulates airway development in fetal lungs, potentially leading to new therapeutic targets for bronchopulmonary dysplasia.

SourceUniversity of Delaware·JournalCellular and Molecular Bioengineering·DateOct 15, 2018

Can you smell through your lungs?

Researchers discovered two olfactory receptors in human lung tissue that regulate airway smooth muscle cell contraction. Activation of these receptors may help constrict or prevent airway constriction in diseases such as asthma and emphysema.

SourceFrontiers·JournalFrontiers in Physiology·DateNov 3, 2016

'Transient contractions' in urinary bladder may lead to therapeutic interventions for bladder dysfunction

Researchers have found that transient bladder contractions play a crucial role in sensing pressure and conveying information to sensory nerves. The frequency and rate of rise of these contractions may be fine-tuned by other cell types, offering potential targets for therapeutic intervention in urinary bladder dysfunction.

SourceRockefeller University Press·JournalJournal of General Physiology·DateMar 28, 2016

Severe asthma: Gallopamil confirmed as a therapeutic approach

Researchers from INSERM have demonstrated gallopamil's clinical efficacy in treating severe asthma by reducing bronchial smooth muscle mass and airway obstruction. The study involved 31 patients with severe asthma, who showed significant improvements in BSM thickness and asthma attacks after treatment.

SourceINSERM (Institut national de la santé et de la recherche médicale)·JournalAmerican Journal of Respiratory and Critical Care Medicine·DateFeb 19, 2015

Racing the clock to help young patients with old hearts

A study by University of Maryland researchers has identified a toxic protein that damages muscle cells inside the arteries of children with progeria, a rare genetic disorder. The discovery may help explain how cardiovascular disease develops in people aging normally and could lead to new treatments for the condition.

SourceUniversity of Maryland·JournalProceedings of the National Academy of Sciences·DateMay 19, 2014