R. Ramasamy et al., Attenuation of ischemia induced increases in sodium and calcium by the aldose reductase inhibitor Zopolrestat, CARDIO RES, 42(1), 1999, pp. 130-139
Citations number
38
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Objective: We have previously demonstrated that zopolrestat, an inhibitor o
f the enzyme aldose reductase, reduces ischemic injury in hearts from diabe
tic and non-diabetic rats. To further explore potential cardioprotective me
chanisms of zopolrestat, we measured changes in intracellular sodium, calci
um, and Na+,K+-ATPase activity in zopolrestat treated hearts during ischemi
a and reperfusion. Methods: Hearts from acute diabetic (Type I) and age-mat
ched control rats were isolated and retrogradely perfused. Hearts had eithe
r control perfusion or exposure to 1 mu M zopolrestat for 10 min, followed
by 20 min of global ischemia and 60 min of reperfusion. Changes in intracel
lular sodium and calcium were measured using Na-23 and F-19 magnetic resona
nce spectroscopy, respectively, while the activity of Na+,K+-ATPase was mea
sured using biochemical assays. Results: Zopolrestat blunted the rise in [N
a](i) during ischemia in both diabetic hearts and non-diabetic hearts. The
end-ischemic [Na](i) was 21.3+/-2.6 mM in the zopolrestat treated diabetics
and 25.9+/-2.3 in zopolrestat treated non-diabetics, versus 31.6+/-2.6 mM
and 32.9+/-2.8 mM in the untreated diabetics and untreated non-diabetics, r
espectively. (P=0.002). Similarly, the rise in [Ca](i) at the end of ischem
ia was significantly reduced in zopolrestat treated diabetic and non-diabet
ic hearts (P=0.005). Zopolrestat increased the activity of Na+,K+-ATPase in
diabetic hearts under baseline conditions (11.70+/-0.95 versus 7.28+/-0.98
mu mol/h/mg protein, P=0.005) as well as during ischemia and reperfusion.
Similar changes in Na+,K+-ATPase activity were also observed in non-diabeti
c hearts. Conclusions: The data provide additional support to the protectiv
e effects of zopolrestat and suggest that a possible mechanism of action ma
y be associated with the attenuation of the rise in [Na](i) and [Ca](i) dur
ing ischemia and reperfusion. (C) 1999 Elsevier Science B.V. All rights res
erved.