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| | Pramlintide - Wikipedia, the free encyclopedia |
 | | It is derived from amylin, a hormone that is released into the bloodstream, in a similar pattern as insulin, after a meal. |
 | | By substituting for amylin, pramlintide aids in the absorption of glucose by slowing gastric emptying, promoting satiety, and the inhibiting inappropriate secretion of glucagon, a catabolic hormone that opposes the effects of insulin and amylin. |
 | | Since native human amylin is highly amyloidogenic and potentially toxic, the strategy for designing pramlintide was to substitute residues from rat amylin, which is not amyloidogenic (but would presumably retain clinical activity). |
| en.wikipedia.org /wiki/Pramlintide (293 words) |
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