Hypertension (Dallas, Tex. : 1979) · 2004
Hypertension and insulin resistance are not directly related in obese dogs.
СтатьяПоддержка службы здравоохранения СШАНазвание и аннотация: Перевод в очереди
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Rocchini Albert P, Yang John Q, Gokee Amy
Аннотация
In dogs fed a high-fat diet, we determined whether there was a direct relation between obesity-induced insulin resistance and obesity-induced hypertension. Thirty-six adult mongrel dogs were chronically instrumented and assigned to receive either a high-fat diet alone (n=7) or a high-fat diet combined with a low-sodium diet plus furosemide (n=6), prazosin plus atenolol (n=7), clonidine (n=10), or aspirin (n=6). Blood pressure, heart rate, and body weight were measured daily. Insulin resistance was assessed with a single-dose euglycemic hyperinsulinemic clamp (2 mU x kg(-1) x min(-1)) before and after 1, 3, and 6 weeks of the high-fat diet. The low-salt diet plus furosemide, prazosin plus atenolol, and clonidine treatments prevented the hypertension associated with feeding the dogs a high-fat diet. Only clonidine treatment totally prevented the development of insulin resistance, and high-dose aspirin, known to prevent insulin resistance by inhibition of the activity of IkappaB kinase-beta, decreased the degree of insulin resistance by almost 70%. However, aspirin had no effect on the development of hypertension. We conclude that obesity-induced hypertension and obesity-induced insulin resistance are not directly related. In addition, there is a suggestion that insulin resistance in this experimental model is mediated through the central and or peripheral alpha2-adrenoceptors, whereas hypertension is mediated through the alpha1- and or beta-adrenoceptors.
Предметные рубрики MeSH
Adrenergic beta-AntagonistsAnimalsAspirinAtenololBlood GlucoseClonidineDiet, Sodium-RestrictedDietary FatsDogsFemaleFurosemideHemodynamicsHypertensionI-kappa B KinaseInsulinInsulin ResistanceMaleModels, AnimalModels, BiologicalObesityPrazosinProtein Serine-Threonine KinasesReceptors, Adrenergic, beta-1Receptors, Adrenergic, beta-2Sympathetic Nervous System