Tb. Creczynski-pasa et al., Complexes trans-[RuCl2(nic)(4)] and trans-[RuCl2(i-nic)(4)] as free radical scavengers, J INORG BIO, 86(2-3), 2001, pp. 587-594
This study evaluates the action of the new ruthenium complexes trans-RuCl2(
nic)(4)] (I) and trans-[RuCl2(i-nic)(4)] (II) as free radical scavengers. I
n our experiments, both compounds acted as scavengers of superoxide anion (
O-2(.-)), hydroxyl radicals (HO.) and nitrogen monoxide (formally known as
'nitric oxide'; NO.). In addition, complexes I and II potentiated the relea
se of NO. from S-nitroso-N-acetyl-DL-penicilamine (SNAP), a NO. donor. Comp
lex E, but not I, also decreased the nitrite levels in culture media of act
ivated macrophages. A hypsochromic shift of lambda (max) and a significant
change in half-wave potential (E-1/2) was observed when NO. was added to th
e Complex II. Thiobarbituric reactive substance (TBARS) levels were signifi
cantly reduced in rats treated for 1 week with Complex H plus tert-butylhyd
roperoxide, when compared to rats treated only with tert-butylhydroperoxide
. None of the complexes showed cytotoxicity. These findings support the sug
gestion that the new ruthenium complexes, especially trans-[RuCl2(i-nic)(4)
] or its derivatives, might provide potential therapeutic benefits in disor
ders where reactive nitrogen (RNS) or oxygen (ROS) species are involved. (C
) 2001 Elsevier Science B.V. All rights reserved.