alexa Effect of the Pleiotropic Drug CNB-001 on Tissue Plasmi
ISSN: 2155-9562

Journal of Neurology & Neurophysiology
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Research Article

Effect of the Pleiotropic Drug CNB-001 on Tissue Plasminogen Activator (tPA) Protease Activity in vitro: Support for Combination Therapy to Treat Acute Ischemic Stroke

Paul A Lapchak1,2* and Paul D Boitano1

1Departments of Neurology Advanced Health Sciences Pavilion, Los Angeles, USA

2Neurosurgery, Cedars-Sinai Medical Center, Advanced Health Sciences Pavilion, Los Angeles, USA

Corresponding Author:
Paul A Lapchak
Director of Translational Research
Cedars-Sinai Medical Center Professor
Department of Neurology & Neurosurgery
Advanced Health Sciences Pavilion, Suite 8305
127 S. San Vicente Blvd, Los Angeles, CA 90048, USA
Tel: 310-248-8188
Fax: 310-248-7568
E-mail: [email protected]

Received date: June 10, 2014; Accepted dat: June 24, 2014; Published date: June 30, 2014

Citation: Lapchak PA, Boitano PD (2014) Effect of the Pleiotropic Drug CNB-001 on Tissue Plasminogen Activator (tPA) Protease Activity in vitro: Support of Combination Therapy to Treat Acute Ischemic Stroke. J Neurol Neurophysiol 5:214. doi:10.4172/2155-9562.1000214

Copyright: © 2014 Lapchak PA, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

 

Abstract

Current state-of-the-art acute ischemic stroke clinical trials are designed to study neuroprotectants when
administered following thrombolysis; tissue plasminogen activator (tPA) is administered to patients within 3-4.5
hours of an ischemic event. Thus, in order to develop a novel neuroprotectant and move it forward to a clinical trial, it
is important to assess the effects of the drug on tPA’s proteolytic activity in vitro, prior to extensive in vivo analysis.
In this study, we determined if CNB-001 [4-((1E)-2-(5-(4-hydroxy-3-methoxystyryl-)-1-phenyl-1H-pyrazoyl-3-
yl)vinyl)-2-methoxy-phenol)], would affect, either enhance or inhibit tPA activity in vitro. In this tPA-inhibitor
(plasminogen activator inhibitor-1; PAI-1 and 2,7-Bis-(4-Amidinobenzylidene)-Cycloheptan-1-One Dihydrochloride;
tPA stop) controlled study, we used a chromogenic substrate (CH3SO2-D-hexahydrotyrosine-Gly-Arg-pnitroanilide•
AcOH) to study drug interactions in vitro, spectrophotometrically measuring protease released p-
Nitroaniline from the substrate.
We found that PAI-1 (0.25 μM) and tPA stop (5 μM) significantly (p<0.0001) inhibited substrate release, by 98.6%
and 83.4%, respectively, thus inhibiting tPA activity in vitro. In comparison, CNB-001 (0.7-7 μM) reduced tPA activity
by 28-32%, with an extrapolated IC50 value of 65.2-704 μM. Thus, although high concentrations of CNB-001 does
affects tPA activity in vitro, the study supports the use of CNB-001 in combination with tPA to treat stroke, However,
CNB-001 should be administered following thrombolysis to promote neuroprotection and repair.

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