Durmus N, Toylu A, Evcim S, Soner B C, Demir O, Kahraman E, Demir T, Irer B, Gidener S, Atabey N, Esen A
Department of Pharmacology, Faculty of Medicine, Dokuz Eylul University, Izmir, Turkey.
Department of Medical Biology, Faculty of Medicine, University of Akdeniz, Izmir, Turkey.
Int J Impot Res. 2017 May;29(3):115-119. doi: 10.1038/ijir.2017.5. Epub 2017 Mar 16.
Hyperlipidemia is an important risk factor for atherosclerosis and is frequently seen in patients with erectile dysfunction (ED). This study was designed to evaluate whether the acute effect of native low-density lipoprotein (nLDL) on intracavernosal pressure (ICP) is reversible and related to plasma asymmetrical dimethylarginine (ADMA), endogenous inhibition of endothelial nitric oxide synthase (eNOS) levels and eNOS expression in cavernous tissues. Hyperlipidemia was induced by a single dose of intravenous 4 mg kg nLDL. Experiments were performed 72 h (72H), 2 weeks (2W) and 8 weeks (8W) after nLDL injection. Endothelium-dependent relaxations, the ratio of ICP to mean arterial pressure (MAP; ICP/MAP), plasma ADMA levels and eNOS mRNA and protein levels were evaluated. The ICP/MAP ratio decreased in both the 2W and 8W groups. Endothelium-dependent relaxation responses to acetylcholine in the rat thoracic aorta were damaged in the 8W group. Plasma ADMA levels increased in the 8W group. mRNA expression of eNOS decreased in a time-dependent manner, whereas the protein expression increased. These results suggest that acute nLDL injection-induced impairments in erectile functions during an 8-week period are irreversible and might be related to an increase in ADMA levels and changes in the regulation of the eNOS/NO pathway.
高脂血症是动脉粥样硬化的重要危险因素,在勃起功能障碍(ED)患者中很常见。本研究旨在评估天然低密度脂蛋白(nLDL)对海绵体内压(ICP)的急性作用是否可逆,以及是否与血浆不对称二甲基精氨酸(ADMA)、内皮型一氧化氮合酶(eNOS)的内源性抑制水平和海绵体组织中eNOS的表达有关。通过单次静脉注射4mg/kg nLDL诱导高脂血症。在nLDL注射后72小时(72H)、2周(2W)和8周(8W)进行实验。评估内皮依赖性舒张、ICP与平均动脉压的比值(MAP;ICP/MAP)、血浆ADMA水平以及eNOS mRNA和蛋白水平。2W和8W组的ICP/MAP比值均降低。8W组大鼠胸主动脉对乙酰胆碱的内皮依赖性舒张反应受损。8W组血浆ADMA水平升高。eNOS的mRNA表达呈时间依赖性下降,而蛋白表达增加。这些结果表明,急性注射nLDL在8周内引起的勃起功能损害是不可逆的,可能与ADMA水平升高以及eNOS/NO途径调节的变化有关。