It is possible to functionally detect pulmonary hypertension at an earlier time point, meaning that interventions could potentially take place sooner.

TOP INSIGHT
Oxidative stress and inflammation can lead to problems such as pulmonary hypertension - increased pressure in the blood vessels of the lung - which increases the mortality and long-term problems in infants.
Progress developing improved treatments for the disease has been limited in part by the lack of advanced imaging techniques to detect pulmonary hypertension and lung damage at earlier time points in animal models, which is important to test these potential new treatments. This model could also help researchers better understand how pulmonary hypertension develops, which is an important aspect of Shivanna's research. So the team set out to develop a mouse model of the disease that replicates many of the features observed in infants with the condition.
To induce oxidative stress and inflammation - two contributing factors of the development of the disease - the researchers exposed a group of newborn mice to 70 percent of oxygen or hyperoxia for 14 days, while a control group received 21 percent oxygen or regular air.
The mice exposed to hyperoxia developed lung oxidative stress, inflammation and lungs that resembled those typical of bronchopulmonary dysplasia and pulmonary hypertension in infants. Furthermore, echocardiography tests performed in the young mice showed that the animals had also developed pulmonary hypertension.
"It's important to understand not only the pathology, but also the functional aspect of pulmonary hypertension," said Shivanna. "This is where the echocardiography test, a non-invasive test that uses high frequency sound waves to take pictures of the heart, comes in."
Source-Eurekalert
MEDINDIA




Email










