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Zhenwu Zhuang, MD, MS

Senior Research Scientist in Medicine (Cardiology)
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Contact Info

Cardiovascular Medicine

& Radiology & Biomedical Imaging, 773C, 300 George Street

New Haven, CT 06511

United States

About

Titles

Senior Research Scientist in Medicine (Cardiology)

Biography

My research focuses on multi-modality cardiovascular, respiratory, and tumoral imaging to visualize and quantify angiogenesis, arteriogenesis, permeability, and organ function; this encompasses 4 common themes: developing novel contrast agents, applying new molecular probes, exploring new algorithms for imaging reconstruction, and finding new applications in myocardial infarction (MI), ischemic stroke, Alzheimer's disease (AD) or cardiac arrest (CA) models.

My significant efforts are directed at:

1. Ischemic stroke & Alzheimer's disease (AD)

2. Coronary microvascular disease

3. Cardiac arrest

I have a broad background in Radiology, Interventional Radiology, Molecular Imaging, and Translational Medicine, with specific training and expertise in multiple research areas, including my surgical and interventional skills, immunohistochemical staining, small animal imaging (microPET/microCT), and imaging analysis.

Appointments

Other Departments & Organizations

Education & Training

MS
Nanjing Medical College (1996)
MD
Nanjing Medical College (1989)

Research

Overview

Novel molecular imaging for early detection of microthrombi in the microvasculature. The exact mechanism and importance of coronary microvascular disease (MVD) under conditions of ischemic injury are still unclear. Based on two notions: 1) endothelial cells can be damaged, and platelets can be activated by photosensitizers irradiated by a specific wavelength of the laser in the heart of a mouse; 2) coagulation factor XIII is required for the impairment of microvascular function progress, we are establishing a novel animal model of MVD and applying non-invasive imaging strategy to monitor cross-linking thrombi formation dynamically and to document subsequent cardiac function in rodents following ischemic injury.

Molecular Imaging of Histone Deacetylase 6 Activity as an Epigenetic Biomarker in Ischemic Stroke. Cerebral ischemic injury is thought to result from a cascade of events ranging from energy depletion, excitotoxicity, oxidative stress, neuroinflammation, and programmed cell death to neuron survival and growth. Despite advances in genetic mechanisms, tissue plasminogen activator (tPA) infusion, or mechanical thrombectomy, the clinical outcome of ischemic stroke remains disappointing. Unlike genetic regulation, epigenetic dysregulation, which does not change the DNA sequence, could be a pathological hallmark of ischemic stroke, triggering multiple events at different stages after ischemic insult. HDAC6 is a unique histone deacetylase (HDAC) subtype that participates in multiple pathological events of ischemic stroke. In preliminary studies, we found that HDAC6 antigen and protein expression levels had increased in the ischemic region in the early stages of stroke in mice. We also found that an HDAC6 inhibitor, ACY-775, effectively mitigated infarct size and improved neurological recovery in mice. Based upon these initial results, we hypothesize that HDAC6 is a specific biomarker for the severity of cerebral ischemic injury and that suppression of HDAC6 activity can rescue neurons from hypoxic damage by an ischemic attack.

PET imaging of Pre-synaptic Vesicle Density for cognitive dysfunction in Cardiac Arrest.

Sudden cardiac arrest (CA) accounts for 50% of all cardiovascular deaths in the US. Despite advances in post-resuscitation care and management, only 10.8% of adult out-of-hospital CA (OHCA) victims survive hospital discharge, and up to 50% of survived patients exhibit cognitive deficits (learning/memory disabilities, executive function). It is well-accepted that cognitive dysfunction is associated with synaptic dysfunction and the inability to induce physiological long-term potentiation (LTP) in the CA1 region of the hippocampus after global ischemia. These deficits suggest that synaptic dysfunction in specific regions (such as the hippocampus or cortex) might be responsible for post-CA brain injury (PCABI). In addition, levels of impairment or recovery of neurologic function govern long-term outcomes after CA, and predicting the potential for recovery is a heavy burden for physicians and patients’ families. A sensitive and reliable in vivo approach to assessing the loss and partial restoration of synaptic function or density can provide early information on the severity of synaptic dysfunction, monitor neuron recovery, and predict the outcome.

Medical Subject Headings (MeSH)

Cardiology; Coronary Disease; Fibrinolysis; Genetic Therapy; Microscopy; Nanoparticles; Phenotype; Radiology, Interventional; Thrombosis

Research at a Glance

Yale Co-Authors

Frequent collaborators of Zhenwu Zhuang's published research.

Publications

2024

2022

2015

2013

2012

2011

Get In Touch

Contacts

Mailing Address

Cardiovascular Medicine

& Radiology & Biomedical Imaging, 773C, 300 George Street

New Haven, CT 06511

United States