Life Desk :
Scientists have found a new and safer antiplatelet drug based on snake venom. The newly designed molecule could help to prevent side effects like excessive bleeding, which is observed in the antiplatelet drugs used at present.
A new and safer antiplatelet drug from snake venom has been designed recently by a research team from the National Taiwan University.
Antiplatelet drugs are widely used to treat heart disease. They could help to prevent blood cells called platelets from clumping together and forming blood clots. However, excessive bleeding after injury is a serious side effect of current antiplatelet drugs.
‘A new antiplatelet drug from snake venom has been designed. It prevents excessive bleeding, a side effect associated with currently used drugs.’
The research team has now designed a drug which could interact with protein glycoprotein VI (GPVI) that is capable of sitting on the surface of the platelets.
The study was published in an an American Heart Association journal, Arteriosclerosis, Thrombosis and Vascular Biology.
Snake venom to develop drugs
The research team found that Trowaglerix, a protein in the venom of the Tropidolaemus waglerix snake has the ability to stimulate platelets in the formation of blood clots by fastening GPVI.
Previous studies have shown that platelets missing GPVI will not form blood clots in patients and may not lead to severe bleeding. More recently, scientists thought that blocking the GPVI could help to prevent blood clotting and also avoid the side effect of prolonged bleeding.
Designing new molecule
The research study is the first to design a molecule that is based on the structure of trowaglerix to block the GPVI activity.
The molecule was found to prevent the platelets from clotting when it was mixed with blood. When the new drug was administered to mice, it had a slower blood clot formation than the untreated mice.
What are Platelets?
Platelets are born in the bone marrow and are released into the circulating blood. Around an average of trillion platelets survive for a week in an adult patient.
They are actually capable of instantaneously plugging to the bleeding sites by sticking on to a wound that becomes activated locally and then attracting other circulating platelets to build an impermeable clump at the point of damage.
Antiplatelet drugs
Aspirin, used commonly to treat pain and fever, was found to be effective for the treatment of heart attacks due to its action on platelets.
Currently available antiplatelet drugs like abciximab is a monoclonal antibody that could act against the platelet membrane protein (GP IIb/IIIa complex) which initiates aggregation. This class of drugs is widely used for treating acute coronary syndromes.
Another class of antiplatelet drugs that were used are called ADP receptor antagonists like ticlopidine, clopidogrel to reduce the occlusion of coronary stents.
The new drugs could help to prevent vascular disease by improving or adding to the beneficial actions of aspirin.
However, currently available antiplatelet drugs target another protein called glycoprotein IIb/IIIa. These drugs were based on another protein that is found in the snake venom. But the reason for excessive bleeding as a side effect is not fully understood.
The novel molecule designed from snake venom could be efficient in developing a new, safer class of antiplatelet drugs with limited bleeding.
Further drug testing in animals and humans is required before it can be used in patients.
Jane Tseng, Ph.D., director and professor at Graduate Institute of Biomedical Electronics and Bioinformatics and Drug Research Center at the National Taiwan University, said, “In general, this type of molecule design does not last long in the body, so techniques like formulation or delivery system are likely needed to extend the exposure time in the human body.”
“The design must also be optimized to ensure that the molecule only interacts with GPVI and not other proteins which can cause unintended reactions.”
He also added that efforts to improve the molecule’s design are underway.
Source: Medindia
Scientists have found a new and safer antiplatelet drug based on snake venom. The newly designed molecule could help to prevent side effects like excessive bleeding, which is observed in the antiplatelet drugs used at present.
A new and safer antiplatelet drug from snake venom has been designed recently by a research team from the National Taiwan University.
Antiplatelet drugs are widely used to treat heart disease. They could help to prevent blood cells called platelets from clumping together and forming blood clots. However, excessive bleeding after injury is a serious side effect of current antiplatelet drugs.
‘A new antiplatelet drug from snake venom has been designed. It prevents excessive bleeding, a side effect associated with currently used drugs.’
The research team has now designed a drug which could interact with protein glycoprotein VI (GPVI) that is capable of sitting on the surface of the platelets.
The study was published in an an American Heart Association journal, Arteriosclerosis, Thrombosis and Vascular Biology.
Snake venom to develop drugs
The research team found that Trowaglerix, a protein in the venom of the Tropidolaemus waglerix snake has the ability to stimulate platelets in the formation of blood clots by fastening GPVI.
Previous studies have shown that platelets missing GPVI will not form blood clots in patients and may not lead to severe bleeding. More recently, scientists thought that blocking the GPVI could help to prevent blood clotting and also avoid the side effect of prolonged bleeding.
Designing new molecule
The research study is the first to design a molecule that is based on the structure of trowaglerix to block the GPVI activity.
The molecule was found to prevent the platelets from clotting when it was mixed with blood. When the new drug was administered to mice, it had a slower blood clot formation than the untreated mice.
What are Platelets?
Platelets are born in the bone marrow and are released into the circulating blood. Around an average of trillion platelets survive for a week in an adult patient.
They are actually capable of instantaneously plugging to the bleeding sites by sticking on to a wound that becomes activated locally and then attracting other circulating platelets to build an impermeable clump at the point of damage.
Antiplatelet drugs
Aspirin, used commonly to treat pain and fever, was found to be effective for the treatment of heart attacks due to its action on platelets.
Currently available antiplatelet drugs like abciximab is a monoclonal antibody that could act against the platelet membrane protein (GP IIb/IIIa complex) which initiates aggregation. This class of drugs is widely used for treating acute coronary syndromes.
Another class of antiplatelet drugs that were used are called ADP receptor antagonists like ticlopidine, clopidogrel to reduce the occlusion of coronary stents.
The new drugs could help to prevent vascular disease by improving or adding to the beneficial actions of aspirin.
However, currently available antiplatelet drugs target another protein called glycoprotein IIb/IIIa. These drugs were based on another protein that is found in the snake venom. But the reason for excessive bleeding as a side effect is not fully understood.
The novel molecule designed from snake venom could be efficient in developing a new, safer class of antiplatelet drugs with limited bleeding.
Further drug testing in animals and humans is required before it can be used in patients.
Jane Tseng, Ph.D., director and professor at Graduate Institute of Biomedical Electronics and Bioinformatics and Drug Research Center at the National Taiwan University, said, “In general, this type of molecule design does not last long in the body, so techniques like formulation or delivery system are likely needed to extend the exposure time in the human body.”
“The design must also be optimized to ensure that the molecule only interacts with GPVI and not other proteins which can cause unintended reactions.”
He also added that efforts to improve the molecule’s design are underway.
Source: Medindia
