A unique molecular target, lead compounds, and established assay systems to assess new compounds to treat vascular stiffening.

About

Background The world health organization has recently identified hypertension as the number 1 risk factor for premature death in the world. As well, the population in many countries is rapidly aging leading to an increasing prevalence of hypertension. Isolated systolic hypertension is the most common form of hypertension in the elderly. It is associated with substantial mortality and morbidity. Although many anti-hypertensives exist, these treatments often fail to regulate the systolic blood pressure without lowering the diastolic pressure making treatment of isolated systolic hypertension difficult. Technology Overview Vascular stiffening with age and the deposition of collagen in the blood vessel wall is an important determinant of hypertension. The increased workload of the heart in this circumstance, due to aortic stiffening, results in left ventricular hypertrophy and chronic heart disease. Researchers at McMaster University target this vascular fibrosis induced by hypertension in the blood vessel wall to reverse the underlying pathology that drives blood pressure higher with aging. The researchers have a unique molecular target, Inositol- requiring enzyme 1 (IRE1)/X-box binding protein 1 spliced (XBP1s) mediated protein synthesis, lead compounds, and established assay systems in vitro and in vivo to assess the ability of novel compounds to inhibit the target.

Applications

• The technology will help to determine novel antihypertensives that prevent end organ damage and lower systolic hypertension in animal models. • This new knowledge is of particular importance to address the health needs of the aging population by preventing the end organ damage related to vascular fibrosis observed in this population.

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