Reiter Martina, Walf Vanessa M, Christians Arne, Pfaffl Michael W, Meyer Heinrich H D
Physiology Weihenstephan, Technische Universität München, Weihenstephaner Berg 3, 85354 Freising, Germany.
Anal Chim Acta. 2007 Mar 14;586(1-2):73-81. doi: 10.1016/j.aca.2006.10.049. Epub 2006 Nov 7.
With this feasibility study a first step towards a new monitoring system for hormonal treatments was done. Screening of regulation and function of anabolic sex steroids via modified gene expression of mRNA in various tissues could be a new approach to trace treatments with unknown drugs or newly combined cocktails. In the study, uterus, liver and muscle tissue from 24 cycling heifers were taken after the animals were treated either with Melengestrol Acetate (MGA), Finaplix-H (200 mg Trenbolone Acetate) or Ralgro (36 mg Zeranol) for 56 days. In every treatment group always two heifers were given 1-fold, 3-fold and 10-fold doses of the standard preparation, the control group without any treatment consisted of two animals. The different tissue gene expression profiles were investigated via the candidate gene approach. Totally 57 candidate genes were selected according to their functionality by screening the actual literature and composed to functional groups: angiogenesis, apoptosis, cell cycle, endocrine factors, energy metabolism, inflammatory factors, muscle function, oncogenes, protein metabolism and transcription factors. Gene expression was measured using quantitative real-time RT-PCR (qRT-PCR) technology. From 24 tested candidate genes in the liver, 17 showed a significant regulation. Eight genes were influenced by MGA, 9 by Finaplix-H, and 4 by Ralgro. For the muscle tissue 19 genes were tested with the result that in the neck muscle 11 genes were regulated and in the hind limb muscle 8 genes. In the neck 5 genes were affected by MGA, 6 by Finaplix-H and 3 by Ralgro. Only 2 genes were influenced by MGA in the hind limb muscle. Finaplix-H affected 6 and Ralgro 4 genes. In the uterus 29 target genes were tested and 13 were significantly influenced by the anabolic sex steroids. Under Finaplix-H treatment eight target genes were regulated and Ralgro and MGA showed a significant regulation in four target genes. The highest gene expression changes under anabolic treatment were observed in the uterus. The analyzed genes showed significant regulations but further studies, testing different animal husbandry conditions will be needed to identify meaningful expression patterns for the different tissues. With the investigation of the regulation and possible function of anabolic sex steroids via gene expression, a preparatory work for the development of an expression pattern for drug screening was made.
通过这项可行性研究,朝着建立一种新的激素治疗监测系统迈出了第一步。通过各种组织中mRNA的基因表达修饰来筛选合成代谢性类固醇的调节和功能,可能是一种追踪未知药物或新组合药物鸡尾酒治疗的新方法。在该研究中,对24头处于发情周期的小母牛进行处理,分别用醋酸美仑孕酮(MGA)、法尼普利-H(200mg醋酸群勃龙)或拉格罗(36mg玉米赤霉醇)处理56天,之后采集子宫、肝脏和肌肉组织。在每个治疗组中,总是有两头小母牛分别给予标准制剂1倍、3倍和10倍剂量,未接受任何处理的对照组由两头动物组成。通过候选基因方法研究不同组织的基因表达谱。通过筛选现有文献,根据其功能共选择了57个候选基因,并将其组成功能组:血管生成、细胞凋亡、细胞周期、内分泌因子、能量代谢、炎症因子、肌肉功能、癌基因、蛋白质代谢和转录因子。使用定量实时RT-PCR(qRT-PCR)技术测量基因表达。在肝脏中检测的24个候选基因中,有17个显示出显著调节。8个基因受MGA影响,9个受法尼普利-H影响,4个受拉格罗影响。对于肌肉组织,检测了19个基因,结果显示颈部肌肉中有11个基因受到调节,后肢肌肉中有8个基因受到调节。在颈部,5个基因受MGA影响,6个受法尼普利-H影响,3个受拉格罗影响。在后肢肌肉中,只有2个基因受MGA影响。法尼普利-H影响6个基因,拉格罗影响4个基因。在子宫中检测了29个靶基因,其中13个受合成代谢性类固醇显著影响。在法尼普利-H处理下,8个靶基因受到调节,拉格罗和MGA在4个靶基因中显示出显著调节。在合成代谢治疗下,子宫中观察到最高的基因表达变化。分析的基因显示出显著调节,但需要进一步研究,测试不同的畜牧条件,以确定不同组织中有意义的表达模式。通过基因表达研究合成代谢性类固醇的调节和可能功能,为开发用于药物筛选的表达模式做了前期工作。