Sieber-Ruckstuhl N S, Meli M L, Boretti F S, Gönczi E, Lutz H, Reusch C E
Clinic for Small Animal Internal Medicine, Clinical Laboratory, Vetsuisse Faculty University of Zurich, Zurich, Switzerland.
Horm Metab Res. 2007 Aug;39(8):548-54. doi: 10.1055/s-2007-985142.
The 11beta-hydroxysteroid dehydrogenase (11beta-HSD) exists in two isoforms, 11beta-HSD1 and 11beta-HSD2. 11beta-HSD1 generates active cortisol from cortisone and appears to be involved in insulin resistant states. 11beta-HSD2 protects the mineralocorticoid receptor from inappropriate activation by glucocorticoids and is important to prevent sodium retention and hypertension. The purposes of the present study were to develop two real-time PCR assays to assess 11beta-HSD1 and 11beta-HSD2 mRNA expression and to evaluate the tissue distribution of the two isoforms in dogs. Thirteen different tissues of 10 healthy dogs were evaluated. Both real-time PCR assays were highly specific, sensitive and reproducible. Highest 11beta-HSD1 mRNA expression was seen in liver, lung, and renal medulla; highest 11beta-HSD2 mRNA expression in renal cortex, adrenal gland, and renal medulla. Higher 11beta-HSD1 than 11beta-HSD2 mRNA levels were found in all tissues except adrenal gland, colon, and rectum. Our results demonstrate that the basic tissue distribution of 11beta-HSD1 and 11beta-HSD2 in dogs corresponds to that in humans and rodents. In a next step 11beta-HSD1 and 11beta-HSD2 expression should be assessed in diseases like obesity, hypercortisolism, and hypertension to improve our knowledge about 11beta-HSD activity, to evaluate the dog as a model for humans and to potentially find new therapeutic options.
11β-羟基类固醇脱氢酶(11β-HSD)有两种同工型,即11β-HSD1和11β-HSD2。11β-HSD1可将可的松转化为活性皮质醇,似乎与胰岛素抵抗状态有关。11β-HSD2可保护盐皮质激素受体免受糖皮质激素的不当激活,对预防钠潴留和高血压很重要。本研究的目的是开发两种实时PCR检测方法,以评估11β-HSD1和11β-HSD2的mRNA表达,并评估这两种同工型在犬体内的组织分布。对10只健康犬的13种不同组织进行了评估。两种实时PCR检测方法均具有高度特异性、敏感性和可重复性。11β-HSD1的mRNA在肝脏、肺和肾髓质中表达最高;11β-HSD2的mRNA在肾皮质、肾上腺和肾髓质中表达最高。除肾上腺、结肠和直肠外,所有组织中11β-HSD1的mRNA水平均高于11β-HSD2。我们的结果表明,犬体内11β-HSD1和11β-HSD2的基本组织分布与人类和啮齿动物的相似。下一步,应在肥胖、皮质醇增多症和高血压等疾病中评估11β-HSD1和11β-HSD2的表达,以增进我们对11β-HSD活性的了解,评估犬作为人类模型的价值,并有可能找到新的治疗方法。