Augmented thromboxane generation by mesenteric arteries from pancreatectomized diabetic dogs is coincident with the vascular tone enhancement evoked by Na arachidonate and prostacyclin

We studied the relationships between acrachidonic acid (AA) metabolism and contractile responses to Na arachidonate (NaA) and the prostaglandins (PGs) in mesenteric arteries isolated from sham-operated and totally pancreatectomized dogs. PGE2 and PGF2α produced a similar dose-dependent relaxation of...

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Autor principal: Sterin-Borda, L.
Otros Autores: Franchi, A.M, Borda, E.S, Castillo, E.D, Gimeno, M.F, Gimeno, A.L
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 1984
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Acceso en línea:Registro en Scopus
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LEADER 15485caa a22016097a 4500
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003 AR-BaUEN
005 20230518204939.0
008 190411s1984 xx ||||fo|||| 00| 0 eng|d
024 7 |2 scopus  |a 2-s2.0-0021162854 
024 7 |2 cas  |a 5,8,11,14 icosatetraynoic acid, 1191-85-1; acetylsalicylic acid, 493-53-8, 50-78-2, 53663-74-4, 53664-49-6, 63781-77-1; haloperidol, 52-86-8; imidazole, 1467-16-9, 288-32-4; indometacin, 53-86-1, 74252-25-8, 7681-54-1; insulin, 9004-10-8; nordihydroguaiaretic acid, 500-38-9; phentolamine, 50-60-2, 73-05-2; phentolamine mesylate, 65-28-1; prostacyclin, 35121-78-9, 61849-14-7; prostaglandin synthase, 39391-18-9, 59763-19-8, 9055-65-6; thromboxane, 66719-58-2; tranylcypromine, 13492-01-8, 155-09-9, 54-97-7; Arachidonic Acid, 506-32-1; Arachidonic Acids; Dinoprost, 551-11-1; Dinoprostone, 363-24-6; Epoprostenol, 35121-78-9; Prostaglandins; Prostaglandins E; Prostaglandins F; Thromboxanes 
040 |a Scopus  |b spa  |c AR-BaUEN  |d AR-BaUEN 
030 |a EJPHA 
100 1 |a Sterin-Borda, L. 
245 1 0 |a Augmented thromboxane generation by mesenteric arteries from pancreatectomized diabetic dogs is coincident with the vascular tone enhancement evoked by Na arachidonate and prostacyclin 
260 |c 1984 
270 1 0 |m Gimeno, A.L.; Centro de Estudios Farmacológicos y de Principios Naturales (CEFAPRIN), Instituto de Biología y Medicina Experimental, Consejo Nacional de Investigaciones Cientificas y Tecnicas de la Republica Argentina (CONICET), Serrano 665/69, 1414 Buenos Aires, Argentina 
506 |2 openaire  |e Política editorial 
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504 |a Aznavoorian, Utsunomiya, Krausz, Cohn, Shepro, Hechtman, Prostacyclin inhibits 5-hydroxytryptamine release but stimulates thromboxane synthesis during cardiopulmonary bypass (1983) Prostaglandins, 25, p. 557 
504 |a Belo, Talesnik, Coronary vasoconstrictor and vasodilator actions of arachidonic acid in the isolated perfused heart of the rat (1982) Br. J. Pharmacol., 75, p. 768 
504 |a Borda, Del C. Agostini, Sterin-Speziale, Gimeno, Gimeno, Spontaneous contractile activity of isolated ovarian human vein. Influence of PGI2 (1979) Prostaglandins, 18, p. 829 
504 |a Borda, Sterin-Borda, Gimeno, Lazzari, Gimeno, The stimulatory effect of prostacyclin (PGI2) on isolated rabbit and rat aorta is probably associated to the generation of a thromboxane A2 (TXA2)-‘like material’ (1983) Arch. Int. Pharmacodyn., 261, p. 79 
504 |a Carreras, Chamone, Klerck, Vermylen, Decreased vascular PGI2 in diabetic rats. Stimulation of PGI2 release in normal and diabetic rats by the antithrombotic compounds Bay 6575 (1980) Thromb. Res., 19, p. 663 
504 |a Christlieb, Janka, Kraus, Gleason, Icadas-Cabral, Aiello, Cabral, Solano, Vascular reactivity to angiotensin II and to norepinephrine in diabetic subjects (1976) Diabetes, 25, p. 268 
504 |a Colwell, Chambere, Laimin, Increased platelet aggregation in early diabetes (1975) Diabetes, 24, p. 684 
504 |a Dusting, Moncada, Vane, Prostacyclin is the endogenous metabolite responsible for relaxation of coronary arteries induced by arachidonic acid (1977) Prostaglandins, 13, p. 3 
504 |a Ellis, Oelz, Roberts, Payne, Sweetman, Nies, Dates, Coronary arterial smooth muscle contraction by a substance released from platelets. Evidence that it is TXA2 (1976) Science, 193, p. 1135 
504 |a Feigen, Chapnick, Hyman, King, Maroscalvo, Kadowitz, Peripheral vasodilator effects of prostaglandins. Comparison of 6-keto PGE1 with PGI2 and escape from PGE2 in mesenteric vascular bed (1980) J. Pharmacol. Exp. Ther., 217, p. 528 
504 |a Ganda, Pathogenesis of macrovascular disease in the human diabetes (1980) Diabetes, 29, p. 931 
504 |a Gerrard, Stuart, Rao, Steffes, Mauer, Brown, White, Alteration in the balance of prostaglandin and thromboxane synthesis in diabetic rats (1980) J. Lab. Clin. Med., 95, p. 950 
504 |a Gimeno, Sterin-Borda, Borda, Lazzari, Gimeno, Human plasma transforms PGI2 into a platelet antiaggregatory substance which contracts isolated bovine coronary arteries (1980) Prostaglandins, 9, p. 907 
504 |a Gimeno, Sterin-Borda, Borda, Del Castillo, Gimeno, Arachidonate evokes constriction of coronary and mesenteric arteries isolated from diabetic dogs (1983) Advances in Prostaglandin, Thromboxane and Leukotriene Research, 12, p. 235. , B. Samuelsson, R. Paoletti, P. Ramwell, Raven Press, New York 
504 |a Gryglewski, Prostaglandin and thromboxane biosynthesis inhibitors (1977) Naunyn-Schmiedeb. Arch. Pharmacol., 297, p. 585 
504 |a Gryglewski, Bunting, Moncada, Flower, Vane, Arterial walls are protected against deposition of platelet thrombin by a substance (PGX), which they may from prostaglandin endoperoxide (1976) Prostaglandins, 12, p. 685 
504 |a Halushka, Rogers, Loadholt, Colwell, Increased platelet thromboxane synthesis in diabetes mellitus (1981) J. Lab. Clin. Med., 97, p. 87 
504 |a Hamberg, On the formation of thromboxane B2 and 12L-hydroxy-5,8,10,14-eicosatetraenoic (12 OH-20:4) in tissues from guinea pig (1976) Biochim. Biophys. Acta, 431, p. 651 
504 |a Hamberg, Samuelsson, Prostaglandin endoperoxides. Novel transformation of arachidonic acid in human platelets (1974) Proc. Natl. Acad. Sci. U.S.A., 71, p. 3400 
504 |a Hamberg, Svensson, Samuelsson, Thromboxanes a new group of biologically active compounds derived from prostaglandin endoperoxides (1975) Proceedings of the National Academy of Sciences, 72, p. 2991 
504 |a Ingerman-Wojenski, Silver, Smith, Macarale, Bovine endothelial cells in culture produce thromboxane as well as prostacyclin (1981) J. Clin. Invest., 67, p. 1292 
504 |a Karper, Pritchard, Jr., Merola, Panganamala, Alterations of the prostacyclin-thromboxane ratio in streptozotocin induced diabetics rats (1982) Prostaglandins, Leukotrienes and Medicine, 8, p. 93 
504 |a Moncada, Biological importance of prostacyclin (1982) Br. J. Pharmacol., 76, p. 31 
504 |a Moncada, Bunting, Mullane, Thorazood, Vane, Imidazole: a selective inhibitor of thromboxane synthetase (1977) Prostaglandins, 13, p. 611 
504 |a Moncada, Gryglewski, Bunting, Vane, An enzyme isolated from arteries transforms prostaglandin endoperoxides to an unstable substance that inhibits platelet aggregation (1976) Nature (London), 263, p. 663 
504 |a Needleman, Kulkerni, Raz, Coronary tone modulation, formation and actions of prostaglandins endoperoxides and thromboxanes (1977) Science, 195, p. 409 
504 |a Nugteren, Jouvenaz, Dutilh, Determinations of prostaglandins and other products of arachidonate oxygenation in perfusates and during platelet aggregation (1978) Acta Biol. Med. Germ., 27, p. 701 
504 |a Owen, Carrier, Alteration in vascular smooth muscle sensitivity to vasoconstrictor agents by streptozotocin-induced diabetes (1979) Proc. West. Pharmacol. Soc., 22, p. 363 
504 |a Rosen, Schrör, Increased prostacyclin release from perfused hearts of acutely diabetic rats (1980) Diabetologia, 18, p. 391 
504 |a Roth, Riebel, Lefer, Vascular responsiveness and eicosanoid production in diabetic rats (1983) Diabetología, 24, p. 372 
504 |a Salzman, Salmon, Moncada, Prostacyclin and thromboxane A2 synthesis by rabbit pulmonary artery (1980) J. Pharmacol. Exp. Ther., 215, p. 240 
504 |a Schrör, Moncada, Obatuba, Vane, Transformation of arachidonic acid and prostaglandin endoperoxides by the guinea pig heart Formation of RCS and prostacyclin (1978) European Journal of Pharmacology, 47, p. 103 
504 |a Sterin-Borda, Borda, Del Castillo, Gimeno, Gimeno, Mechanism of coronary vasoconstriction induced by Na arachidonate in experimental diabetic dogs (1982) Experientia, 38, p. 835 
504 |a Sterin-Borda, Borda, Gimeno, Lazzari, Del Castillo, Gimeno, Contractile activity and prostacyclin generation in isolated coronary arteries from diabetic dogs (1982) Diabetología, 22, p. 56 
504 |a Sterin-Borda, Canga, Borda, Gimeno, Gimeno, Inotropic effect of PGI2 on isolated rat atria at different contraction frequency (1980) Naunyn-Schmiedeb. Arch. Pharmacol., 313, p. 95 
504 |a Tuvemo, Strandberg, Hamberg, Samuelsson, Formation and action of prostaglandin endoperoxides in the isolated human umbilical artery (1976) Acta Physiol. Scand., 96, p. 145 
504 |a Urgoiti, Houssay, Rietti, Hypophyseal and adrenal factors essential for ketoacidosis of pancreatectomized dogs (1963) Diabetes, 12, p. 301 
504 |a Vane, Inhibition of prostaglandin synthesis as a mechanism of action for aspirin-like dugs (1971) Nature New Biol., 231, p. 232 
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504 |a Wicks, Rose, Johnson, Ramwell, Kot, Vascular responses to arachidonic acid in the perfused canine lung (1976) Circ. Res., 38, p. 167 
504 |a Wolfe, Rostworowski, Manku, Measurement of prostaglandin synthesis and release from rat aortic tissue and from the perfused mesenteric artery by gas chromatographic mass spectrometric methods (1979) Prostacyclin, p. 113. , J.R. Vaner, S. Bergström, Raven Press, New York 
504 |a Wong, Malik, Desiderio, McGiff, Sun, Hepatic metabolism of prostacyclin in the rabbit: formation of a potent novel inhibitor of platelet aggregation (1980) Biophys. Res. Commun., 93, p. 486 
520 3 |a We studied the relationships between acrachidonic acid (AA) metabolism and contractile responses to Na arachidonate (NaA) and the prostaglandins (PGs) in mesenteric arteries isolated from sham-operated and totally pancreatectomized dogs. PGE2 and PGF2α produced a similar dose-dependent relaxation of mesenteric arteries from normal and diabetic dogs. On the contrary, NaA and prostacyclin (PGI2) enhanced the resting basal tone of arteries from pancreatectomized animals but depressed it in arteries from intact normal control or from sham-operated groups. Inhibitors of thromboxane A2 (TXA2) biosynthesis abolished in vitro the vasoconstricting effect of NaA and PGI2 in diabetics whereas inhibitors of PGI2 biosynthesis blocked the vasodilating influence of NaA in normal mesenteric vessels. Additionally, antagonists of cycooxygenase activity prevented both the vasoconstricting and the vasodilating actions of NaA in normal and in diabetic arteries, respectively, as well as the PGI2 tone enhancement in vessels from diabetics. In arteries from pancreatectomized animals treated with insulin, PGI2 induced a biphasic (constriction and relaxation) effect of a magnitude between that of effects seen in normal controls or sham-operated and those in untreated diabetic animals. The basal radioconversion of exogenous [1-14C]AA, showed that mesenteric arteries from diabetic dogs generated more TXB2 than did vessels from intact normal control or sham-operated dogs. Moreover, in the presence of exogenous PGI2, the vascular production of TXB2 from AA in the diabetic group was significantly greater than that of preparations not exposed to PGI2. The % conversion of AA into PGI2 (assessed as 6-oxo-PGF1α) was similar in normal controls, in sham-operated and in diabetic vessels. Insulin given in vivo abolished the greater basal conversion of AA into TBX2 by mesenteric arteries from diabetic dogs and significantly attenuated the enhanced prostacyclin-evoked generation of thromboxane. The present results strongly suggest that the abnormal constricting response evoked by NaA and PGI2 in mesenteric arteries from diabetic dogs could be related to the generation of TXA2 by vessel walls. © 1984.  |l eng 
536 |a Detalles de la financiación: Consejo Nacional de Investigaciones Científicas y Técnicas 
536 |a Detalles de la financiación: * This work was supported by grants (6638) from the Consejo Nacional de lnvestigaciones Cientificas y T6cnicas de la Repfiblica Argentina (CONICET) and by the Fundaci6n Alberto J. Roemmers, Buenos Aires, Argentina. 
593 |a Centro de Estudios Farmacológicos y de Principios Naturales (CEFAPRIN), Instituto de Biología y Medicina Experimental, Consejo Nacional de Investigaciones Cientificas y Tecnicas de la Republica Argentina (CONICET), Serrano 665/69, 1414 Buenos Aires, Argentina 
690 1 0 |a 6-OXO-PGF1Α 
690 1 0 |a ARACHIDONIC ACID 
690 1 0 |a ARTERIES 
690 1 0 |a CYCLOOXYGENASE 
690 1 0 |a INSULIN 
690 1 0 |a LIPOXYGENASE 
690 1 0 |a MESENTERIC VESSELS 
690 1 0 |a PANCREATECTOMIZED DOGS 
690 1 0 |a PROSTACYCLIN 
690 1 0 |a PROSTAGLANDINS 
690 1 0 |a THROMBOXANE 
690 1 0 |a VASOCONSTRICTION 
690 1 0 |a VASODILATION 
690 1 0 |a 5,8,11,14 ICOSATETRAYNOIC ACID 
690 1 0 |a ACETYLSALICYLIC ACID 
690 1 0 |a ARACHIDONIC ACID C 14 
690 1 0 |a HALOPERIDOL 
690 1 0 |a IMIDAZOLE 
690 1 0 |a INDOMETACIN 
690 1 0 |a INSULIN 
690 1 0 |a NORDIHYDROGUAIARETIC ACID 
690 1 0 |a PHENTOLAMINE 
690 1 0 |a PHENTOLAMINE MESYLATE 
690 1 0 |a PROSTACYCLIN 
690 1 0 |a PROSTAGLANDIN SYNTHASE 
690 1 0 |a RADIOISOTOPE 
690 1 0 |a THROMBOXANE 
690 1 0 |a TRANYLCYPROMINE 
690 1 0 |a UNCLASSIFIED DRUG 
690 1 0 |a ANIMAL MODEL 
690 1 0 |a ARTICLE 
690 1 0 |a DIABETES MELLITUS 
690 1 0 |a DOG 
690 1 0 |a DRUG EFFICACY 
690 1 0 |a ENDOCRINE SYSTEM 
690 1 0 |a MESENTERIC ARTERY 
690 1 0 |a NONHUMAN 
690 1 0 |a PANCREAS RESECTION 
690 1 0 |a PERIPHERAL VASCULAR SYSTEM 
690 1 0 |a ANIMALS 
690 1 0 |a ARACHIDONIC ACID 
690 1 0 |a ARACHIDONIC ACIDS 
690 1 0 |a DIABETES MELLITUS, EXPERIMENTAL 
690 1 0 |a DINOPROST 
690 1 0 |a DINOPROSTONE 
690 1 0 |a DOGS 
690 1 0 |a EPOPROSTENOL 
690 1 0 |a MESENTERIC ARTERIES 
690 1 0 |a MUSCLE TONUS 
690 1 0 |a MUSCLE, SMOOTH, VASCULAR 
690 1 0 |a PANCREATECTOMY 
690 1 0 |a PROSTAGLANDINS 
690 1 0 |a PROSTAGLANDINS E 
690 1 0 |a PROSTAGLANDINS F 
690 1 0 |a THROMBOXANES 
690 1 0 |a VASOCONSTRICTION 
650 1 7 |2 spines  |a DIABETES 
650 1 7 |2 spines  |a PANCREAS 
653 0 0 |a haldol; regitine 
700 1 |a Franchi, A.M. 
700 1 |a Borda, E.S. 
700 1 |a Castillo, E.D. 
700 1 |a Gimeno, M.F. 
700 1 |a Gimeno, A.L. 
773 0 |d 1984  |g v. 103  |h pp. 211-221  |k n. 3-4  |p Eur. J. Pharmacol.  |x 00142999  |w (AR-BaUEN)CENRE-1772  |t European Journal of Pharmacology 
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856 4 0 |u https://hdl.handle.net/20.500.12110/paper_00142999_v103_n3-4_p211_SterinBorda  |y Handle 
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