Researchers at the University of Illinois at Chicago have developed a replacement drug that forestalls blood
clots without causing an increased risk of bleeding, a standard side effect of all antiplatelet medications
currently available. A new study published within the journal Science Translational Medicine describes the
drug and its delivery mechanisms and shows that the drug is additionally an efficient treatment for attack in
animal models. Xiaoping Du, UIC professor of pharmacology and regenerative medicine at the College of
Medicine, led the research. “Unfortunately, current antiplatelet medications prevent the blood coagulation
that cause attack and stroke but also disrupt platelets’ ability to prevent bleeding if a vessel is torn,” Du said.
“In some cases, severe bleeding can be life-threatening. The magic of this new drug is it prevents clots but
does not make people prone to bleeding, which other drugs have failed to do.” In a previous study, Du and
his colleagues identified a signaling mechanism that is important in the blood clotting process but not
required for platelets’ ability to adhere to a wound and prevent bleeding. Based on this finding, the
researchers derived a peptide to target the signaling mechanism and designed a nanoparticle that
successfully delivered the peptide into platelets.
Du said a attack can cause coronary failure and death in two alternative ways . One, from the initial
damage caused by the clot, which blocks blood flow and reduces oxygen supply. This typically is
treated by a procedure called angioplasty and a stent to open the artery, combined with
antiplatelet drugs to prevent it from clotting again. However, fresh blood flowing into the
damaged heart tissue following the reopening of the artery can trigger inflammation, causing
leaks and clots in small blood vessels and further damage to the heart, Du said. Xiaoping Du
(Photo:
Joshua Clark) “This is named reperfusion injury and this is often the second way a attack can
cause
coronary failure or death,” Du said. “We were hopeful that this new drug, which doesn't
cause vessel
leaks, would help limit reperfusion injury and reduce the prospect of coronary failure and death,
and our
hypothesis was proved correct — we saw very promising results from our study.” In the study,
among mice that received the treatment, administered as an injection, there was reduced
damage to the heart, reduced clotting and reduced inflammation.
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