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Generic name: Tolbutamide
Common names: Artosin, Novo-Butamide, Orinase.

A brand of Rastinon labelled as Tolbutamide is at Easy MD

MedicationStrengthQuantityPriceEasy MD
Tolbutamide500 mg10 tablets$59.98Order
Tolbutamide500 mg20 tablets$97.98Order
Tolbutamide500 mg30 tablets$137.98Order
Tolbutamide500 mg60 tablets$253.98Order
Tolbutamide500 mg90 tablets$369.98Order

All medications at Easy MD are generics.



Description: Rastinon (Tolbutamide) is used to treat type II (noninsulin-dependent) diabetes (formerly 'adult-onset'), particularly in people whose diabetes cannot be controlled by diet alone. Rastinon (Tolbutamide) lowers blood sugar by stimulating the pancreas to secrete insulin and helping the body use insulin efficiently. The pancreas must produce insulin for this drug to work. Rastinon (Tolbutamide) is not used to treat type I (insulin-dependent) diabetes (formerly 'juvenile-onset'). A doctor may prescribe Rastinon (Tolbutamide) for additional conditions. Click for more Rastinon details.


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HealthCare News

Heart Attack Damage Control

Background: A heart attack is not a simple event. It involves anoccluded (blocked) blood vessel or vessels in the heart muscle. Thisblockage results in oxygen deprivation which in turn stimulates the productionof a protein called vascular endothelial growth factor (VEGF). In the longrun, VEGF production is good because it promotes the growth of new blood vesselsthat can makea detouraround the blockagebut in the short run,VEGF causes vessels to leak andthat results in fluid buildup and tissuedamagein the heart muscle.

Study: Research in mice demonstrated that it is possible to limit theleaky effect of VEGF by blocking an enzyme called Src kinase. (The article inthe Journal of Clinical Investigation poetically referred to Src as a"myocardial shark"). Mice genetically deficient in Src or normal micetreated with pharmacological Src inhibitors showed minimal vascularpermeability, edema and platelet microthrombi following a heart attack. Thesemice exhibited not only dramatically reduced infarct volume early on, but also adecrease in fibrosis and mortality months after the injury. Importantly, asingle dose of an Src inhibitor given up to 6 hours after injury still providedcardiac protection.

Comment: All of this suggests that care must be exercised in the clinicaluse of VEGF to promote the growth of new blood vessels in the heart. And it alsosuggeststhat blockading Src may reduce tissue injury followingaheart attackand perhaps after similar events elsewhere in the body.Nowto go from mice to men.

Barbara K. Hecht,Ph.D.
Frederick Hecht, M.D.
Medical Editors, MedicineNet.com

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