AI Article Synopsis

  • - Pulmonary arterial hypertension (PAH) is a serious lung disease that currently has no cure, highlighting the need for new treatment options.
  • - The mouse hypoxia-induced PAH model is effective for studying the disease and testing new therapies, as it mimics human symptoms of PAH.
  • - This protocol provides detailed guidance on how to perform multiple intravenous injections and assess heart function in this model, addressing technical challenges that researchers face.

Article Abstract

Pulmonary arterial hypertension (PAH) is a progressive life-threatening disease, primarily affecting small pulmonary arterioles of the lung. Currently, there is no cure for PAH. It is important to discover new compounds that can be used to treat PAH. The mouse hypoxia-induced PAH model is a widely used model for PAH research. This model recapitulates human clinical manifestations of PAH Group 3 disease and is an important research tool to evaluate the effectiveness of new experimental therapies for PAH. Research using this model often requires the administration of compounds in mice. For a compound that needs to be given directly into the bloodstream, optimizing intravenous (IV) administration is a key part of the experimental procedures. Ideally, the IV injection system should permit multiple injections over a set time course. Although the mouse hypoxia-induced PAH model is very popular in many laboratories, it is technically challenging to perform multiple IV bolus dosing and invasive hemodynamic assessment in this model. In this protocol, we present step-by-step instructions on how to carry out multiple IV bolus dosing via mouse jugular vein and perform arterial and right ventricle catheterization for hemodynamic assessment in mouse hypoxia-induced PAH model.

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Source
http://dx.doi.org/10.3791/63839DOI Listing

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