Myogenic responsiveness is a regulator of cerebral blood flow autoregulation. Diseases disrupting this critical function can reduce perfusion and threaten the integrity of brain tissue. QP’s pre-clinical studies in heart failure and subarachnoid hemorrhage models identified a molecular mechanism underlying cerebral microvascular dysfunction that can be treated with a drug that is that is now being trialled in patients.
Learn about our
LYRIC-HF trial.
Total Peripheral Resistance (TPR) defines the resistance to blood flow created by the circulatory system - a key determinant of blood pressure alongside cardiac output. In the peripheral microcirculation, skeletal muscle resistance arteries govern 30-40% of TPR, representing a compelling target for therapies. QP identified a molecular mechanism driving TPR in skeletal arteries and is now screening targets to advance a novel treatment of arterial hypertension.