Moraga Fernando A, Miranda Giselle, López Vasthi, Vallejos Carmen, Silva Daniel
Laboratory of Physiology, Hypoxia and Vascular Function, Department of Biomedical Science, Faculty of Medicine, Universidad Católica del Norte, Coquimbo, Chile .
High Alt Med Biol. 2018 Jun;19(2):149-155. doi: 10.1089/ham.2017.0012. Epub 2018 Mar 22.
Moraga, Fernando A., Giselle Miranda, Vasthi López, Carmen Vallejos, and Daniel Silva. Chronic intermittent hypobaric hypoxia (4600 M) attenuates pulmonary vasodilation induced by acetylcholine or sodium nitroprusside. High Alt Med Biol. 19:149-155, 2018.
Previous studies performed in rats exposed to chronic intermittent hypobaric hypoxia (CIHH), at a simulated altitude of 4600 m, showed reduced nitric oxide (NO) production, increased arginase activity, and increased oxidative stress. However, studies on vascular function are scarce. Our aim was to measure plasma nitrate and nitrite (NOx) concentration and study pulmonary vascular function in rats exposed to CIHH in the presence of potassium chloride (KCl), acetylcholine (Ach), and sodium nitroprusside (SNP).
Thirty male Wistar rats were divided into two groups: A control group (normoxia (N), n = 10) and a CIHH group (2N × 2H × 30 days, n = 20). CIHH exposure was performed in a hypobaric chamber at 428 Torr (4600 m). Noninvasive systolic blood pressure (SBP), heart rate, and body weight (BW) were measured. Blood samples were obtained to measure NOx levels and hematocrit (Hct). CIHH animals that gained BW and presented a Hct <20% and maintained SBP were classified as tolerant, and animals that lost >30% of their BW, increased Hct and SBP >20% were classified as intolerant. Animals were sacrificed and small pulmonary arteries (SPA) were obtained to perform concentration-response curves to KCl, Ach, and SNP.
Intolerant rats (30%) had decreased NOx levels. SPA had a larger vasocontraction response to KCl and a lower dilation response to SNP in the SPA compared to tolerant and control animals. In addition, SPA had a lower dilatation response to Ach compared with the control. Together, these results show that CIHH alters endothelium-dependent vasodilation.
莫拉加,费尔南多·A.,吉赛尔·米兰达,瓦斯蒂·洛佩斯,卡门·巴列霍斯,以及丹尼尔·席尔瓦。慢性间歇性低压缺氧(4600米)减弱乙酰胆碱或硝普钠诱导的肺血管舒张。《高原医学与生物学》。第19卷:第149 - 155页,2018年。
先前在模拟海拔4600米的环境中对暴露于慢性间歇性低压缺氧(CIHH)的大鼠进行的研究表明,一氧化氮(NO)生成减少、精氨酸酶活性增加以及氧化应激增加。然而,关于血管功能的研究很少。我们的目的是测量血浆硝酸盐和亚硝酸盐(NOx)浓度,并研究在存在氯化钾(KCl)、乙酰胆碱(Ach)和硝普钠(SNP)的情况下暴露于CIHH的大鼠的肺血管功能。
30只雄性Wistar大鼠分为两组:对照组(常氧(N),n = 10)和CIHH组(2天常氧×2天缺氧×30天,n = 20)。在428托(4600米)的低压舱中进行CIHH暴露。测量无创收缩压(SBP)、心率和体重(BW)。采集血样以测量NOx水平和血细胞比容(Hct)。体重增加、Hct < 20%且SBP维持稳定的CIHH动物被归类为耐受型,体重减轻> 30%、Hct升高且SBP升高> 20%的动物被归类为不耐受型。处死动物并获取小肺动脉(SPA)以进行对KCl、Ach和SNP的浓度 - 反应曲线实验。
不耐受型大鼠(30%)的NOx水平降低。与耐受型和对照组动物相比,SPA对KCl的血管收缩反应更大,对SNP的舒张反应更低。此外,与对照组相比,SPA对Ach的舒张反应更低。总之,这些结果表明CIHH会改变内皮依赖性血管舒张。