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首页> 外文期刊>The Journal of Veterinary Medical Science >Renal Effects of Medetomidine in Isoflurane-Anesthetized Dogs with Special Reference to Its Diuretic Action
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Renal Effects of Medetomidine in Isoflurane-Anesthetized Dogs with Special Reference to Its Diuretic Action

机译:美托咪定对异氟烷麻醉狗的利尿作用,特别是其利尿作用

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References(34) Cited-By(8) Renal effects of the selective α2-adrenoceptor agonist, medetomidine, were investigated in anesthetized dogs. Animals were administered medetomidine 20 and 40 μg/kg intravenously (IV) and 80 μg/kg intramuscularly (IM) or 1 ml of saline IV. Urine and blood samples were collected before and at 30, 60, 90 and 120 min following medetomidine injection. Mean arterial blood pressure (MABP), renal blood flow (RBF), glomerular filtration rate (GFR), urine volume (Uv), urine osmolality (Uosm), free water clearance (CH2O), fractional clearance of sodium (FNa), plasma osmolality (Posm), plasma glucose levels and plasma antidiuretic hormone (ADH) concentrations were measured. The results showed that IV administration of medetomidine initially increased MABP 5-15 min followed by long-lasting decrease. The initial hypertension was not observed after IM administration, which was accompanied by a more profound hypotensive effects. RBF, GFR, Uv, CH2O increased after IV injection and decreased after IM. Medetomidine increased FNa and Posm and decreased Uosm. Plasma glucose levels initially increased and subsequently decreased. Plasma ADH concentration was decreased by IV injection but increased by IM administration. Our data imply that: 1) IV administration of medetomidine at dose rates of 20 and 40 μg/kg results in profound diuresis up to 2 hr; 2) Suppression of ADH release from the CNS is one of the mechanisms of medetomidine-induced diuresis although it may not be the principal one.
机译:参考文献(34)被引用的By(8)在麻醉犬中研究了选择性α2-肾上腺素受体激动剂美托咪定的肾脏作用。给动物静脉内(IV)给予美托咪定20和40μg/ kg,肌肉内(IM)给予80μg/ kg美托咪定或1 ml生理盐水IV。在美托咪定注射之前和之后30、60、90和120分钟收集尿液和血液样本。平均动脉血压(MABP),肾血流量(RBF),肾小球滤过率(GFR),尿量(Uv),尿渗透压(Uosm),游离水清除率(CH2O),钠清除率(FNa),血浆测量了渗透压(Posm),血浆葡萄糖水平和血浆抗利尿激素(ADH)浓度。结果表明,美托咪定的静脉给药最初使MABP增加5-15分钟,然后持续减少。 IM给药后未观察到最初的高血压,并伴有更深刻的降压作用。静脉注射后,RBF,GFR,Uv,CH2O升高,IM后降低。美托咪定增加FNa和Posm并降低Uosm。血浆葡萄糖水平最初升高,随后降低。静脉注射可降低血浆ADH浓度,而IM则可提高血浆ADH浓度。我们的数据表明:1)以20和40μg/ kg的剂量静脉内注射美托咪定可导致长达2个小时的利尿。 2)抑制CNS释放ADH是美托咪定诱导利尿的机制之一,尽管它可能不是主要的机制。

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