Marine snail venom may improve insulin for diabetics

Insulin derived from the venom of marine cone snails may pave the way for a faster-acting drug to treat diabetes, scientists say.
Although moderately mobile, marine cone snails have perfected several strategies to capture prey. Some fish-hunting species release venom into the surrounding water. Within the plume of toxic venom, the fish succumbs to fast-acting insulin that renders it immobile.
As the fish flounders, the snail emerges from its shell to swallow the pacified victim whole. Researchers at University of Utah in the US detailed the function of cone snail insulins, bringing them one step closer to developing a faster-acting insulin to treat diabetes. “These snails have developed a strategy to hit and subdue their prey with up to 200 different compounds, one of which is insulin,” said Helena Safavi-Hemami, assistant professor at University of Utah. “Every now and then, we learn something unique from nature and millions of years of evolution,” said Safavi-Hemami. Insulin, a hormone produced by the pancreas to regulate blood sugar, consists of two segments called A and B chains.
The B cluster forms dimers and hexamers that allow the pancreas to store the hormone for later use. This segment is also necessary to activate the insulin receptors that signal the body to take up sugar from the blood. Insulin must undergo several conversions to decluster before it can lower blood sugar. A person with type 1 diabetes is unable to produce insulin and requires daily injections to manage their blood sugar. Despite decades of research, the manufactured insulin continues to contain the B chain in order to activate the receptor to lower blood sugar, delaying the drug’s effect by 3090 minutes.
Researchers examined the function of seven insulin sequences found in the venom from three species of cone snail Conus geographus, C tulipa and C kinoshitai.
Unexpectedly, each species produces insulin with slightly different structures. Despite these differences, each insulin is fast-acting because it lacks the sticky part of the B chain found in human insulin. (PTI)

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