Bv. Venkataraman et al., DECAVANADATE POSSESSES ALPHA-ADRENERGIC AGONIST ACTIVITY AND A STRUCTURAL MOTIF COMMON WITH TRANS-BETA FORM OF NORADRENALINE, Molecular and cellular biochemistry, 169(1-2), 1997, pp. 27-36
Decavanadate, an inorganic polymer of vanadate, produced contraction o
f rat aortic rings at a relatively high concentration compared to phen
ylephrine, an agonist of alpha-adrenergic receptor. This effect was bl
ocked by two known alpha-adrenergic receptor antagonists, prazosin and
phenoxybenzamine. Decavanadate, formed by possible dimerization of V-
5 under acid conditions, possessed a structural feature of two pairs o
f unshared oxygen atoms at a distance of 3.12 Angstrom, not found in i
ts constituents of V-4 or V-5. A structural motif of O..O..O using suc
h oxygen atoms is recognized in decavanadate. This matches with a simi
lar motif of N..O..O that uses the essential amino and hydroxyl groups
of the side-chain and the m-hydroxyl group in trans-beta form of nora
drenaline. The interaction of such a structural motif with the membran
e receptor is likely to be the basis of the unusual noradrenaline-mimi
c action of decavanadate.