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Erschienen in: CNS Drugs 11/2001

01.11.2001 | Leading Article

Reducing Bleeding Complications After Thrombolytic Therapy for Stroke

Clinical Potential of Metalloproteinase Inhibitors and Spin Trap Agents

verfasst von: Dr Paul A. Lapchak, Dalia M. Araujo

Erschienen in: CNS Drugs | Ausgabe 11/2001

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Abstract

Thrombolysis with alteplase (recombinant tissue plasminogen activator; rtPA) has proven to be beneficial for acute stroke management, despite the narrow window of opportunity for treatment and the increased risk of haemorrhage. Because of the latter, recent studies have attempted to identify compounds that may be given concomitantly with alteplase to reduce the haemorrhage rate
Matrix metalloproteinase (MMP) inhibitors have been proposed as potential combination therapy candidates because they prevent MMP-induced production of the cytokine tumour necrosis factor-α (TNFα), as well as membrane and vessel remodelling following ischaemia. Spin trap agents also have been put forward due to their free radical scavenging capabilities.
In the rabbit large clot embolism model, alteplase effectively lysed blood clots, whether or not other drugs were used in combination. However, haemorrhage rate also was increased compared with that in control animals. The alteplase-induced haemorrhage rate was reduced significantly by administration of the MMP inhibitor batimastat (BB-94) or the spin trap agent α-phenyl-N-t-butylnitrone (PBN). Other rodent studies have also demonstrated that PBN is effective in decreasing the haemorrhage rate following alteplase administration.
Overall, preclinical studies indicate that MMP inhibition or free radical scavenging in combination with alteplase may circumvent the high risk of haemorrhaging with alteplase.
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Metadaten
Titel
Reducing Bleeding Complications After Thrombolytic Therapy for Stroke
Clinical Potential of Metalloproteinase Inhibitors and Spin Trap Agents
verfasst von
Dr Paul A. Lapchak
Dalia M. Araujo
Publikationsdatum
01.11.2001
Verlag
Springer International Publishing
Erschienen in
CNS Drugs / Ausgabe 11/2001
Print ISSN: 1172-7047
Elektronische ISSN: 1179-1934
DOI
https://doi.org/10.2165/00023210-200115110-00001

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