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CURATIVE ISOSORBIDE‐5‐MONONITRATE TREATMENT, IN OPPOSITION TO THE BENEFICIAL PREVENTIVE ONE, AGGRAVATES THE PROTHROMBOTIC AND PROCONSTRICTOR STATE IN CYCLOSPORINE‐INDUCED HYPERTENSIVE RATS
Author(s) -
Reis F,
Ponte L,
Rocha L,
TeixeiraLemos E,
Almeida L,
Alcobia T,
Lourenço M,
Palmeiro A,
FerrerAntunes CA,
CostaAlmeida C,
Teixeira F
Publication year - 2005
Publication title -
clinical and experimental pharmacology and physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.752
H-Index - 103
eISSN - 1440-1681
pISSN - 0305-1870
DOI - 10.1111/j.0305-1870.2005.04244.x
Subject(s) - medicine , thromboxane , thromboxane b2 , isosorbide mononitrate , lipid peroxidation , platelet , blood pressure , pharmacology , oxidative stress
SUMMARY 1. The aim of the present study was to evaluate the effect of preventive and curative isosorbide‐5‐mononitrate (Is‐5‐Mn) treatment on the development of hypertension, cGMP content, thromboxane (TX) A 2 /prostaglandin (PG) I 2 balance, the peripheral serotonergic system, platelet activation, lipid peroxidation and plasma lipids in cyclosporine A (CsA)‐induced hypertensive rats. 2. Control, CsA (5 mg/kg per day) and Is‐5‐Mn (150 mg/kg per day, b.i.d.) rat groups were treated orally over a period of 7 weeks. The preventive Is‐5‐Mn group (Is‐5‐Mn + CsA) was first treated for 2 weeks with Is‐5‐Mn, followed by 7 weeks with both drugs; the curative Is‐5‐Mn group (CsA + Is‐5‐Mn) was treated for a period of 7 weeks with CsA and with both drugs for an additional 5 weeks. The control group received oral vehicle. 3. Whereas in the group undergoing preventive treatment the CsA‐induced increase in blood pressure (BP), compared with the control group, was avoided, in the group undergoing curative treatment, the increase in BP was even higher. The decreased arterial cGMP content in the CsA group was prevented and reverted when Is‐Mn was administered either preventatively or curatively with CsA. Platelet TXA 2 production, although unaffected in the Is‐5‐Mn + CsA group, was significantly higher in the CsA + Is‐5‐Mn group compared with the group receiving CsA alone. Furthermore, plasma TXA 2 was reduced following preventive Is‐5‐Mn treatment, but was worsened in the group undergoing curative therapy. Aortic PGI 2 synthesis was identical in all groups. Consequently, the TXA 2 /PGI 2 ratio was only altered in the CsA + Is‐5‐Mn group, demonstrating a markedly higher value. In both groups treated simultaneously with CsA and Is‐5‐Mn, a higher platelet 5‐hydroxytryptamine (5‐HT) content was obtained compared with CsA treatment alone, but only preventive treatment with Is‐5‐Mn resulted in a significant reduction in plasma 5‐HT. Changes in ADP and collagen‐induced platelet aggregation paralleled those of plasma 5‐HT and TXA 2 : the hyperaggregation profile of the CsA group, although partially prevented, was not reverted by simultaneous treatment with Is‐5‐Mn and CsA. Lipid peroxidation and lipid profile values also worsened in the CsA + Is‐5‐Mn group compared with the group administered CsA alone. 4. In conclusion, the beneficial effects of concomitant Is‐5‐Mn and CsA treatment were demonstrated when Is‐5‐Mn was administered preventatively because not only was arterial hypertension prevented, but platelet aggregation and plasma TXA 2 and 5‐HT levels were also reduced. In contrast, following curative treatment, the BP, platelet/vascular vasoconstrictor balance, lipid peroxidation and plasma lipids were aggravated, recommending a judicious evaluation of the impact of nitrate therapy throughout the period of its administration.