首页> 外文期刊>American Journal of Physiology >Renal interstitial adenosine metabolism during ischemia in dogs.
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Renal interstitial adenosine metabolism during ischemia in dogs.

机译:犬缺血期间的肾间质腺苷代谢。

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摘要

The present study was conducted to determine the metabolism of renal interstitial adenosine under resting conditions and during ischemia. By using a microdialysis method with HPLC-fluorometric analysis, renal interstitial concentrations of adenosine, inosine, and hypoxanthine were assessed in pentobarbital-anesthetized dogs. Average basal renal interstitial concentrations of adenosine, inosine, and hypoxanthine were 0.18 +/- 0.04, 0.31 +/- 0.05, and 0.35 +/- 0.05 micromol/l, respectively. Local inhibition of adenosine kinase with iodotubercidin (10 micromol/l in perfusate) or inhibition of adenosine deaminase with erythro-9-(2-hydroxy-3-nonyl)adenine (EHNA; 100 micromol/l in perfusate) did not change adenosine concentrations in the nonischemic kidneys (0.18 +/- 0.04 and 0.24 +/- 0.05 micromol/l, respectively). On the other hand, treatment with iodotubercidin+EHNA significantly increased adenosine concentration (0.52 +/- 0.07 micromol/l) with significant decreases in inosine and hypoxanthine levels (0.13 +/- 0.03 and 0.19 +/- 0.04 micromol/l, respectively). During 30 min of ischemia, adenosine, inosine, and hypoxanthine were significantly increased to 0.76 +/- 0.29, 2.14 +/- 0.45, and 21.8 +/- 4.7 micromol/l, respectively. The treatment with iodotubercidin did not alter ischemia-induced increase in adenosine (0.84 +/- 0.18 micromol/l); however, EHNA alone markedly enhanced adenosine accumulation (13.54 +/- 2.16 micromol/l), the value of which was not augmented by an addition of iodotubercidin (15.80 +/- 1.24 micromol/l). In contrast, ischemia-induced increases in inosine and hypoxanthine were inversely diminished by the treatment with iodotubercidin+EHNA (0.90 +/- 0.20 and 9.86 +/- 1.96 micromol/l, respectively). These results suggest that both adenosine kinase and adenosine deaminase contribute to the metabolism of renal interstitial adenosine under resting conditions, whereas adenosine produced during ischemia is mainly metabolized by adenosine deaminase and the rephosphorylation of adenosine by adenosine kinase is small.sent
机译:进行本研究以确定在静止状态和局部缺血期间肾间质腺苷的代谢。通过采用微透析方法和HPLC荧光分析,评估了戊巴比妥麻醉犬的肾间质中腺苷,肌苷和次黄嘌呤的浓度。腺苷,肌苷和次黄嘌呤的平均基础肾脏间质浓度分别为0.18 +/- 0.04、0.31 +/- 0.05和0.35 +/- 0.05 micromol / l。碘苯哌丁啶(在灌流液中为10微摩尔/升)对腺苷激酶的局部抑制,或用erythro-9-(2-羟基-3-壬基)腺嘌呤(EHNA;灌流液中为100微摩尔/升)抑制腺苷脱氨酶不会改变腺苷浓度在非缺血性肾脏中(分别为0.18 +/- 0.04和0.24 +/- 0.05 micromol / l)。另一方面,用碘代结核菌素+ EHNA处理可显着增加腺苷浓度(0.52 +/- 0.07微摩尔/升),而肌苷和次黄嘌呤水平则显着降低(分别为0.13 +/- 0.03和0.19 +/- 0.04微摩尔/升)。 。在缺血的30分钟内,腺苷,肌苷和次黄嘌呤分别显着增加至0.76 +/- 0.29、2.14 +/- 0.45和21.8 +/- 4.7微摩尔/升。碘苯哌丁啶的治疗没有改变缺血引起的腺苷增加(0.84 +/- 0.18微摩尔/升)。然而,单独使用EHNA可以显着增强腺苷的积累(13.54 +/- 2.16微摩尔/升),而碘苯丁菊酯(15.80 +/- 1.24微摩尔/升)并不能增加其值。相比之下,缺血诱导的肌苷和次黄嘌呤的增加通过碘代结核菌素+ EHNA(分别为0.90 +/- 0.20和9.86 +/- 1.96 micromol / l)的治疗而被逆向减少。这些结果表明,在静止状态下,腺苷激酶和腺苷脱氨酶均参与肾间质腺苷的代谢,而缺血期间产生的腺苷主要由腺苷脱氨酶代谢,腺苷激酶对腺苷的再磷酸化作用很小。

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