口服生物场能量处理专利试验制剂对维生素d3缺乏症大鼠模型维生素d3代谢产物水平的改善

Jana S
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引用次数: 0

摘要

本实验评估了意识能量治疗(Trivedi效应®)对新型专利试验配方的影响,雄性Sprague Dawley (SD)大鼠喂养维生素D3缺乏症饮食(VDD),以估计肾组织中维生素D3代谢物。一种新的专有测试配方由几种矿物质(镁、锌、铜、钙、硒和铁)、维生素(抗坏血酸、吡哆醇HCl、α生育酚、氰钴胺素和胆钙化醇)、人参提取物、β-胡萝卜素和分离大麻二酚组成。新试验配方分为两部分;一部分被定义为未经处理的测试配方,而另一部分测试配方和动物接受了著名生物场能量治疗师Mahendra Kumar Trivedi先生的生物场能量治疗。生物场能量处理测试配方组(G5)、生物场能量处理本身(G6)和生物场能量处理测试配方(G7)组预处理15天的25-OH维生素d3水平显著提高了21%、22.9%和11.5%。分别与疾病对照组(G2)比较。此外,与G2相比,G6组的125 -(OH) 2 d3水平升高了55%。此外,与G4组相比,G6组肾脏中CYP24A的表达增加了13.9%,而G5、G6、G7(第15天生物场能量处理试验配方)和G8(第15天生物场能量处理本身加生物场能量处理试验配方)组肾脏中CYP27B的表达分别显著增加了17.6%、18.6%、10.1%和15.6%。与G2组相比,G6组和G7组维生素D受体(VDR)表达量分别显著增加69.5%和31%。总的来说,结果显示维生素d3代谢产物的可用性显著改善,这可能有助于维生素d3缺乏症患者保持良好的骨骼健康和免疫力。因此,结果表明,生物场能量治疗组本身和/或生物场能量治疗试验配方组的疾病进展和与疾病相关的所有其他并发症/症状显著减缓。G6、G7、G8、G9)与疾病组比较。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Improvement of Vitamin D 3 Metabolites Level after Oral Administration of the Biofield Energy Treated Proprietary Test Formulation in Vitamin D 3 Deficiency Diet (VDD) Induced Rat Model
The present experiment was evaluated to study of the effect of Consciousness Energy Healing Treatment (the Trivedi Effect ® ) on novel proprietary test formulation in male Sprague Dawley (SD) rats, fed with vitamin D3 deficiency diet (VDD) for the estimation of vitamin D3 metabolites in kidney tissue. A novel proprietary test formulation was formulated with a few minerals (magnesium, zinc, copper, calcium, selenium, and iron), vitamins (ascorbic acid, pyridoxine HCl, alpha tocopherol, cyanocobalamin, and cholecalciferol), Panax ginseng extract, β-carotene, and cannabidiol isolate. The novel test formulation was divided into two parts; one part was defined as the untreated test formulation, while the other part of the test formulation and the animals received Biofield Energy Healing Treatment by a renowned Biofield Energy Healer, Mr. Mahendra Kumar Trivedi. 25-OH vitamin D 3 level was significantly increased in the Biofield Energy Treated test formulation group (G5), Biofield Energy Treatment per se (G6), and 15-days pre-treatment of the Biofield Energy Treated test formulation (G7) groups by 21%, 22.9%, and 11.5%, respectively as compared with the disease control group (G2). Additionally, the level of 1,25-(OH) 2 D 3 was increased by 55% in the G6 group as compared with the G2. Further, the expression of CYP24A in kidney was increased by 13.9% in the G6 group, while CYP27B expression in kidney was significantly increased by 17.6%, 18.6%, 10.1%, and 15.6% in the G5, G6, G7 (Biofield Energy Treated test formulation from day -15), and G8 (Biofield Energy Treatment per se plus Biofield Energy Treated test formulation from day -15) groups, respectively as compared with the G4 group. Vitamin D receptor (VDR) expression was significantly increased by 69.5% and 31% in the G6 and G7 groups, respectively as compared with the G2 group. Overall, the results showed significant improvement of the availability of vitamin D 3 metabolites, that could be helpful for the vitamin D 3 deficiency persons to maintain good bone health and immunity. Therefore, the results suggest that there was significant slowdown in the disease progression and disease related all other complications/symptoms in the Biofield Energy Treatment group per se and/or Biofield Energy Treated Test formulation groups ( viz . G6, G7, G8, and G9) comparatively with the disease group.
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