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Evidence that nitric oxide is an endogenous antiangiogenic mediator
Author(s) -
PipiliSynetos Eva,
Sakkoula Eleni,
Haralabopoulos G.,
Andriopoulou Paraskevi,
Peristeris P.,
Maragoudakis M.E.
Publication year - 1994
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1111/j.1476-5381.1994.tb14822.x
Subject(s) - mediator , nitric oxide , endogeny , chemistry , neuroscience , pharmacology , medicine , microbiology and biotechnology , biology , biochemistry , endocrinology
1 The involvement of nitric oxide (NO) in the regulation of angiogenesis was examined in the in vivo system of the chorioallantoic membrane (CAM) of the chick embryo and in the matrigel tube formation assay. 2 Sodium nitroprusside (SNP) (0.37–28 nmol/disc), which releases NO spontaneously, caused a dose‐dependent inhibition of angiogenesis in the CAM in vivo and reversed completely the angiogenic effects of α‐thrombin (6.7 nmol/disc) and the protein kinase C (PKC) activator 4‐β‐phorbol‐12‐myristate‐13‐acetate (PMA) (0.97 nmol/disc). In addition, SNP (28 × 10 −6 m ) stimulated the release of guanosine 3′‐5′‐cyclic monophosphate (cyclic GMP) from the CAM in vitro . 3 In the matrigel tube formation assay, an in vitro assay of angiogenesis, both SNP (1–3 × 10 −6 m ) and the cell permeable cyclic GMP analogue, Br‐cGMP (0.3–1.0 × 10 −3 m ) reduced tube formation. 4 The inhibitors of NO synthase, N G ‐monomethyl‐ l ‐arginine ( l ‐NMMA) (3.8–102 nmol/disc) and N G ‐nitro‐ l ‐arginine methylester ( l ‐NAME) (1.3–34.2 nmol/disc) stimulated angiogenesis in the CAM in vivo , in a dose‐dependent fashion. d ‐NMMA and d ‐NAME on the other hand had no effect on angiogenesis in this system. 5 l ‐Arginine (10.9 nmol/disc), although it had a modest antiangiogenic effect by itself, was capable of abolishing the angiogenic effects of l ‐NMMA (34.2 nmol/disc) and of l ‐NAME (3.8 nmol/disc). 6 Dexamethasone, an inhibitor of the induction of NO synthase, at 0.2–116.1 nmol/disc, stimulated angiogenesis in the CAM, whereas at 348.4–1161 nmol/disc it inhibited this process. Combination of 38.7 nmol/disc dexamethasone with l ‐NAME (9.3 nmol/disc) resulted in a potentiation of the angiogenic effect of the former. It appears therefore that both the constitutive and the inducible NO synthase may contribute to the NO‐mediated inhibition of angiogenesis. 7 Superoxide dismutase (SOD), which prevents the destruction of NO, at 300 i.u./disc had a modest antiangiogenic effect in the CAM, by itself. In addition, SOD, prevented α‐thrombin (6.7 nmol/disc) and PMA (0.97 nmol/disc) from stimulating angiogenesis in the CAM. 8 These results suggest that NO may be an endogenous antiangiogenic molecule of pathophysiological importance.