Wilson Christopher R, Tran Mai K, Salazar Katrina L, Young Martin E, Taegtmeyer Heinrich
Department of Internal Medicine, Division of Cardiology, University of Texas Medical School at Houston, University of Texas Health Science Center at Houston, 6431 Fannin, MSB 1.246, Houston, TX 77030, USA.
Biochem J. 2007 Sep 15;406(3):457-67. doi: 10.1042/BJ20070392.
Obesity and diabetes are associated with increased fatty acid availability in excess of muscle fatty acid oxidation capacity. This mismatch is implicated in the pathogenesis of cardiac contractile dysfunction and also in the development of skeletal-muscle insulin resistance. We tested the hypothesis that 'Western' and high fat diets differentially cause maladaptation of cardiac- and skeletal-muscle fatty acid oxidation, resulting in cardiac contractile dysfunction. Wistar rats were fed on low fat, 'Western' or high fat (10, 45 or 60% calories from fat respectively) diet for acute (1 day to 1 week), short (4-8 weeks), intermediate (16-24 weeks) or long (32-48 weeks) term. Oleate oxidation in heart muscle ex vivo increased with high fat diet at all time points investigated. In contrast, cardiac oleate oxidation increased with Western diet in the acute, short and intermediate term, but not in the long term. Consistent with fatty acid oxidation maladaptation, cardiac power decreased with long-term Western diet only. In contrast, soleus muscle oleate oxidation (ex vivo) increased only in the acute and short term with either Western or high fat feeding. Fatty acid-responsive genes, including PDHK4 (pyruvate dehydrogenase kinase 4) and CTE1 (cytosolic thioesterase 1), increased in heart and soleus muscle to a greater extent with feeding a high fat diet compared with a Western diet. In conclusion, we implicate inadequate induction of a cassette of fatty acid-responsive genes, and impaired activation of fatty acid oxidation, in the development of cardiac dysfunction with Western diet.
肥胖和糖尿病与脂肪酸供应增加有关,且脂肪酸供应超过了肌肉脂肪酸氧化能力。这种不匹配与心脏收缩功能障碍的发病机制有关,也与骨骼肌胰岛素抵抗的发展有关。我们检验了这样一个假设,即“西方”饮食和高脂肪饮食会不同程度地导致心脏和骨骼肌脂肪酸氧化适应不良,从而导致心脏收缩功能障碍。将Wistar大鼠分别喂食低脂、“西方”或高脂肪(分别来自脂肪的热量为10%、45%或60%)饮食,喂养时间为急性(1天至1周)、短期(4 - 8周)、中期(16 - 24周)或长期(32 - 48周)。在所研究的所有时间点,高脂肪饮食均可使离体心肌中的油酸氧化增加。相比之下,西方饮食在急性、短期和中期可使心脏油酸氧化增加,但在长期则不然。与脂肪酸氧化适应不良一致,仅长期西方饮食会使心脏功能下降。相比之下,比目鱼肌的油酸氧化(离体)仅在急性和短期西方或高脂肪喂养时增加。与西方饮食相比,高脂肪饮食喂养时,心脏和比目鱼肌中包括PDHK4(丙酮酸脱氢酶激酶4)和CTE1(胞质硫酯酶1)在内的脂肪酸反应性基因增加的程度更大。总之,我们认为西方饮食导致心脏功能障碍的过程中,脂肪酸反应性基因盒的诱导不足以及脂肪酸氧化的激活受损。