Enhancement of vascular targeting by inhibitors of nitric oxide synthase

• Published in: International journal of radiation oncology, biology, physics Vol. 54; no. 5; p. 1532
• Main Authors: Davis, Peter D, Tozer, Gillian M, Naylor, Matthew A, Thomson, Peter, Lewis, Gemma, Hill, Sally A
• Format: Journal Article
• Language: English
• Published: United States 01-12-2002
• Subjects: Angiogenesis Inhibitors - therapeutic use; Animals; Antineoplastic Agents, Phytogenic - therapeutic use; Benzimidazoles - pharmacology; Enzyme Inhibitors - pharmacology; Fluorescent Dyes - pharmacology; Mice; Mice, Inbred CBA; Models, Chemical; Necrosis; Neovascularization, Pathologic; Nitric Oxide Synthase - antagonists & inhibitors; Stilbenes - therapeutic use; Time Factors; Tubulin - metabolism; Tumor Cells, Cultured
• ISSN: 0360-3016
• DOI: 10.1016/S0360-3016(02)03925-1

This study investigates the enhancement of the vascular targeting activity of the tubulin-binding agent combretastatin A4 phosphate (CA4P) by various inhibitors of nitric oxide synthases.
The syngeneic tumors CaNT and SaS growing in CBA mice were used for this study. Reduction in perfused vascular volume was measured by injection of Hoechst 33342 24 h after drug administration. Necrosis (hematoxylin and eosin stain) was assessed also at 24 h after treatment. Combretastatin A4 phosphate was synthesized by a modification of the published procedure and the nitric oxide synthase inhibitors L-NNA, L-NMMA, L-NIO, L-NIL, S-MTC, S-EIT, AMP, AMT, and L-TC, obtained from commercial sources.
A statistically significant augmentation of the reduction in perfused vascular volume by CA4P in the CaNT tumor was observed with L-NNA, AMP, and AMT. An increase in CA4P-induced necrosis in the same tumor achieved significance with L-NNA, L-NMMA, L-NIL, and AMT. CA4P induced little necrosis in the SaS tumor, but combination with the inhibitors L-NNA, L-NMMA, L-NIO, S-EIT, and L-TC was effective.
Augmentation of CA4P activity by nitric oxide synthase inhibitors of different structural classes supports a nitric oxide-related mechanism for this effect. L-NNA was the most effective inhibitor studied.