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MAHE researchers discover origin of insulin effects on blood vessels

Published On : 11 Aug 2018   |  Reported By : Courtesy The Hindu   |  Pic On: Photo credit The Hindu


Manipal. (The Hindu): Scientists at the School of Life Sciences (SOLS), Manipal Academy of Higher Education (MAHE), have identified key genes influenced by inflammatory mediator, interleukin-6 (IL-6), on endothelial cells associated with insulin resistance.

“That could be the reason why Type 2 Diabetes (T2D) patients suffer from vascular diseases despite controlling the glucose levels by insulin or anti-diabetic drugs,” said Director, SOLS, K. Satyamoorthy, who is the group leader of the team.

A press release issued by MAHE here recently said that the extensive research was published in the scientific journal, “Laboratory Investigations”, a Springer-Nature journal.

Dr. Satyamoorthy said that the hypothesis behind morbidity associated with vascular diseases in T2D, even after strict control of glucose levels, is due to metabolic memory. “This is based on epigenetic mechanisms and can be regulated by several factors such as inflammation, hyperglycemia, or stress. Hence, studying these epigenetic mechanisms was important and it led to the discovery of new genes and mechanisms,” he said.

Normal levels of IL-6 produced by immune cells protect the body from pathogens during infections.

However, conditions such as diabetes are associated with sterile inflammation and where there is increased production of IL-6 levels, it leads to deleterious effects and may even cause insulin resistance.

Manjunath B. Joshi, primary scientist, added, “It has long been known that the inflammatory molecule IL-6 concentrations are high in serum of T2D patients and we were wondering how IL-6 influences endothelial cells and if there is a role in disturbing insulin function. Our work links high IL-6 levels with decreased insulin function and investigates underlying epigenetic mechanisms.”

Ashwath Balakrishnan, Ph.D scholar associated with the work at MAHE, said, “Epigenetic changes caused by key enzyme, DNMT1 is destabilised in response to IL-6 leading to disturbed production of nitric oxide and hence, insulin is unable to impart its normal function”.

Vinod Bhat, Vice-Chancellor of MAHE, said, “MAHE is supporting molecular genetics programme as there is plenty to discover to the benefit of patients. A majority of T2D subjects suffer from vascular diseases and it is important to study vascular endothelial cells to identify newer therapeutic interventions to restore the normal function of the endothelial cells. MAHE is in unique environment that researchers, clinical practitioners and public health experts can work together to bring about change in society on how diseases are managed in individuals”.







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