Researchers at the Children's Hospital Boston in the USA have discovered a mechanism for normalizing blood sugar that does not involve insulin and could offer a new therapeutic approach to both kinds of diabetes.
Reporting in Nature Medicine online on February 13, Umut Ozcan and colleagues in the Children's Division of Endocrinology show that a regulatory protein called XBP-1s, when activated artificially in the liver, can normalize high blood sugar in both lean, insulin-deficient type 1 diabetic mice and obese, insulin-resistant type 2 diabetic mice. This suggests that approaches aimed at increasing XBP-1s activity may benefit patients with either type of diabetes.
In previous work, Dr Ozcan's lab identified XBP-1s as a key to the body's sensitivity to insulin, and shown that its function is impaired in the presence of obesity. Initially, XBP-1s was thought to increase insulin sensitivity and normalize blood glucose by binding to DNA and relieving stress on the endoplasmic reticulum, a cellular organ that assembles and folds proteins. When XBP-1s was artificially activated, "blood sugars in obese mice with type 2 diabetes came down abruptly," Dr Ozcan says.
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
Copyright © The Pharma Letter 2024 | Headless Content Management with Blaze