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猪在输注多巴酚丁胺时心肌脂肪酸摄取增加,同时丙二酰辅酶A水平降低。

Increased cardiac fatty acid uptake with dobutamine infusion in swine is accompanied by a decrease in malonyl CoA levels.

作者信息

Hall J L, Lopaschuk G D, Barr A, Bringas J, Pizzurro R D, Stanley W C

机构信息

Section of Cardiovascular Pharmacology, Syntex Discovery Research, PaloAlto, CA 94304, USA.

出版信息

Cardiovasc Res. 1996 Nov;32(5):879-85.

PMID:8944819
Abstract

OBJECTIVE

Malonyl CoA is an important regulator of fatty acid oxidation in the heart secondary to its ability to inhibit carnitine palmitoyltransferase 1 (CPT 1). Malonyl CoA is produced from acetyl CoA in a reaction catalyzed by acetyl CoA carboxylase (ACC). In this study we determined if alterations in malonyl CoA regulation of fatty acid metabolism are involved in the increase in energy transduction seen following an increase in cardiac work.

METHODS

Anesthetized, open-chest, domestic swine were subjected to a 30 min control period followed by a 30 min treatment period with either dobutamine (15 micrograms.kg-1. min-1 i.v.) (n = 6) or saline (n = 6).

RESULTS

Heart rate, left ventricular peak dp/dt, and MVO2, were significantly increased in the dobutamine group compared to the saline group during the treatment period. Free fatty acid and glucose uptake were increased 210 and 248%, respectively, in the dobutamine group during the treatment period. Malonyl CoA content was decreased by 55% (from 0.40 +/- 0.05 to 0.18 +/- 0.12 nmol/g wet wt; P < 0.05) with dobutamine treatment, but was not affected by saline treatment. ACC activity was not significantly different between groups (0.31 +/- 0.02 vs. 0.30 +/- 0.04 nmol. min-1. mg protein-1, respectively). The activity of AMP-dependent protein kinase (AMPK), which phosphorylates and inactivates ACC, was also not significantly different in the dobutamine hearts compared to the saline hearts (322 +/- 26 vs. 338 +/- 39 pmol. min-1. mg protein-1, respectively).

CONCLUSION

The increased cardiac work following dobutamine infusion is accompanied by a decrease in malonyl CoA levels and an increase in fatty acid uptake. However, the decrease in malonyl CoA cannot be explained by a decrease in ACC activity.

摘要

目的

丙二酰辅酶A是心脏脂肪酸氧化的重要调节因子,这归因于其抑制肉碱棕榈酰转移酶1(CPT 1)的能力。丙二酰辅酶A由乙酰辅酶A在乙酰辅酶A羧化酶(ACC)催化的反应中生成。在本研究中,我们确定了丙二酰辅酶A对脂肪酸代谢的调节改变是否参与了心脏工作增加后能量转导的增强。

方法

对麻醉的、开胸的家猪进行30分钟的对照期,随后用多巴酚丁胺(15微克·千克⁻¹·分钟⁻¹静脉注射)(n = 6)或生理盐水(n = 6)进行30分钟的治疗期。

结果

在治疗期,多巴酚丁胺组的心率、左心室峰值dp/dt和MVO2相比生理盐水组显著增加。在治疗期,多巴酚丁胺组的游离脂肪酸和葡萄糖摄取分别增加了210%和248%。多巴酚丁胺治疗使丙二酰辅酶A含量降低了55%(从0.40±0.05降至0.18±0.12纳摩尔/克湿重;P < 0.05),但生理盐水治疗未对其产生影响。两组间ACC活性无显著差异(分别为0.31±0.02与0.30±0.04纳摩尔·分钟⁻¹·毫克蛋白⁻¹)。与生理盐水组心脏相比,多巴酚丁胺组心脏中使ACC磷酸化并使其失活 的AMP依赖蛋白激酶(AMPK)活性也无显著差异(分别为322±26与338±39皮摩尔·分钟⁻¹·毫克蛋白⁻¹)。

结论

多巴酚丁胺输注后心脏工作增加伴随着丙二酰辅酶A水平降低和脂肪酸摄取增加。然而,丙二酰辅酶A的降低不能用ACC活性降低来解释。

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