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Profil bibliographique

Zahra Nourian

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

35Publications signalées
388Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

Cardiac electrophysiology and arrhythmiasIon channel regulation and functionNeuroscience and Neuropharmacology ResearchConnective tissue disorders researchMuscle Physiology and Disorders

Les publications récentes

Accès ouvert 2025 article OpenAlex

Small Arteries From Old Spontaneously Hypertensive Rats Exhibit Enhanced Endothelium‐Independent Vasodilatory Capacity and Reduced Stiffness

Francisco I. Ramirez‐Perez, Thomas J. Jurrissen, Marc A. Augenreich, Jorge A. Castorena‐Gonzalez et autres

OBJECTIVE: In conduit arteries, aging and hypertension are associated with stiffening characterized by increased cytoskeletal F-actin and endothelial dysfunction. Herein, we determined if this also happens at the level of the resistance vasculature. METHODS: We retrospectively compared the mechanical and structural characteristics …

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0 citations Microcirculation
Accès ouvert 2024 article OpenAlex

Right ventricular preload and afterload challenge induces contractile dysfunction and arrhythmia in isolated hearts of dystrophin‐deficient male mice

Andrew Behrmann, Jessica Cayton, Matthew R. Hayden, Michelle D. Lambert et autres

Abstract Duchenne muscular dystrophy (DMD) is an X‐linked recessive myopathy due to mutations in the dystrophin gene. Diaphragmatic weakness in DMD causes hypoventilation and elevated afterload on the right ventricle (RV). Thus, RV dysfunction in DMD develops early in disease progression. Herein, …

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1 citation Physiological Reports
Accès ouvert 2023 preprint OpenAlex

Combined Right Ventricular Preload and Afterload Challenge Induces Contractile Dysfunction and Ventricular Arrhythmia in an Age-dependent Manner in Isolated Hearts of Dystrophin-deficient Mice

Andrew Behrmann, Jessica Cayton, Matt Hayden, Michelle Lambert et autres

Abstract Duchenne muscular dystrophy (DMD) is an X-linked recessive myopathy due to mutations in the dystrophin gene. Diaphragmatic weakness in DMD causes restrictive lung disease and excessive afterload on the right ventricle (RV). Thus, RV dysfunction in DMD develops early in disease …

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0 citations bioRxiv (Cold Spring Harbor Laboratory)
Accès ouvert 2023 article OpenAlex

Calcium handling dysfunction and cardiac damage following acute ventricular preload challenge in the dystrophin-deficient mouse heart

V Haffner, Zahra Nourian, Erika M. Boerman, Michelle D. Lambert et autres

The mechanisms of cardiac disease progression in muscular dystrophy are complex and poorly understood. Using a transgenic mouse model with cardiomyocyte-specific expression of the GCaMP6f Ca2+ indicator, the present study provides further support for the Ca2+-overload hypothesis of disease progression and ventricular …

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7 citations American Journal of Physiology-Heart and Circulatory Physiology
Accès ouvert 2023 preprint OpenAlex

Atrial arrhythmogenesis in ex vivo aged mouse hearts with hypokalemia and right atrial stretch

Jessica Cayton, Zahra Nourian, Michelle Lambert, Zhenguo Liu et autres

Abstract Introduction Atrial Fibrillation (AF) and atrial flutter (AFL) are the two most common cardiac arrhythmias in the United States. While advanced age has been correlated to AF/AFL, the lack of an appropriate animal model has hindered progress on better understanding the …

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0 citations bioRxiv (Cold Spring Harbor Laboratory)
Accès ouvert 2023 article OpenAlex

Postnatal development of extracellular matrix and vascular function in small arteries of the rat

Zahra Nourian, Kwangseok Hong, Min Li, Jorge A. Castorena‐Gonzalez et autres

Introduction: Vascular extracellular matrix (ECM) is dominated by elastic fibers (elastin with fibrillin-rich microfibrils) and collagens. Current understanding of ECM protein development largely comes from studies of conduit vessels (e.g., aorta) while resistance vessel data are sparse. With an emphasis on elastin, …

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3 citations Frontiers in Pharmacology
2023 article OpenAlex

The potential role of matrix metalloproteinases on reducing small artery stiffness and improving vasodilation in old spontaneously hypertensive rats

Marc A. Augenreich, Thomas J. Jurrissen, Francisco I. Ramirez‐Perez, Jorge A. Castorena‐Gonzalez et autres

Arterial stiffening is a major risk factor for cardiovascular disease development and progression. Both hypertension and aging are associated with presence of microcirculation endothelial dysfunction, hypercontractility, and vascular stiffening. Reports suggest that while hypertension results in inward remodeling, aging is associated with …

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0 citations Physiology
2023 article OpenAlex

Right ventricular function in hearts of a mouse model of Duchenne muscular dystrophy following increased ventricular load

Michelle Lambert, Andrew Behrmann, Zahra Nourian, Keith Nyanyo et autres

Duchenne muscular dystrophy (DMD) is an X-linked recessive myopathy caused by mutations in the gene encoding dystrophin. Dystrophin is present in striated muscle cells and stabilizes the sarcolemma to mitigate contraction-induced damage. The main cause of death in DMD is cardiopulmonary failure …

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0 citations Physiology
Accès ouvert 2022 article OpenAlex

Modification of Fibronectin by Non-Enzymatic Glycation Impairs K+ Channel Function in Rat Cerebral Artery Smooth Muscle Cells

Yan Yang, Zahra Nourian, Min Li, Zhe Sun et autres

Fibronectin (FN) enhances K+ channel activity by integrin-mediated mechanisms. As vascular smooth muscle (VSM) K+ channels mediate vasodilation, we hypothesized that modification of fibronectin, via advanced non-enzymatic glycation, would alter signaling of this extracellular matrix protein through these channels. Bovine FN (1 …

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5 citations Frontiers in Physiology
2021 article OpenAlex

Ventricular Dysfunction and Calcium Handling Derangements in Isolated Hearts From Duchenne Muscular Dystrophy (DMD mdx‐4CV ) Mice Following Sustained Ventricular Preload

Vivian C. Onyali, Zahra Nourian, Laurin M. Hanft, Maike Krenz et autres

Duchenne muscular dystrophy (DMD) is the most common muscular dystrophy and is caused by mutations in the dystrophin gene. Subclinical signs of cardiac disease present early and usually progress to dilated cardiomyopathy in late stage DMD patients. Dystrophin deficiency associates with stretch‐induced …

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0 citations The FASEB Journal

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