Wouter R. P. H. van de Worp, Jan Theys, Cecile J. A. Wolfs, Frank Verhaegen, Annemie M. W. J. Schols, Ardy van Helvoort, Ramon C. J. Langen
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Here, we investigated the therapeutic effect of an intervention diet consisting of a specific combination of high protein, leucine, fish oil, vitamin D, galacto-oligosaccharides, and fructo-oligosaccharides on the development and progression of cachexia in an orthotopic lung cancer mouse model.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>Eleven-week-old male 129S2/Sv mice were orthotopically implanted with 344P lung epithelial tumour cells or vehicle (control). Seven days post-implantation tumour-bearing (TB) mice were allocated to either intervention- or isocaloric control diet. Cachexia was defined as 5 days of consecutive body weight loss, after which mice were euthanized for tissue analyses.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>TB mice developed cachexia accompanied by significant loss of skeletal muscle mass and epididymal fat mass compared with sham operated mice. The cachectic endpoint was significantly delayed (46.0 ± 15.2 vs. 34.7 ± 11.4 days), and the amount (−1.57 ± 0.62 vs. −2.13 ± 0.57 g) and progression (−0.26 ± 0.14 vs. −0.39 ± 0.11 g/day) of body weight loss were significantly reduced by the intervention compared with control diet. Moreover, systemic inflammation (pentraxin-2 plasma levels) and alterations in molecular markers for proteolysis and protein synthesis, indicative of muscle atrophy signalling in TB-mice, were suppressed in skeletal muscle by the intervention diet.</p>\n </section>\n \n <section>\n \n <h3> Conclusions</h3>\n \n <p>Together, these data demonstrate the potential of this multinutrient intervention, targeting multiple components of cachexia, as integral part of lung cancer management.</p>\n </section>\n </div>","PeriodicalId":48911,"journal":{"name":"Journal of Cachexia Sarcopenia and Muscle","volume":null,"pages":null},"PeriodicalIF":9.4000,"publicationDate":"2024-07-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11446694/pdf/","citationCount":"0","resultStr":"{\"title\":\"Targeted nutritional intervention attenuates experimental lung cancer cachexia\",\"authors\":\"Wouter R. P. 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Here, we investigated the therapeutic effect of an intervention diet consisting of a specific combination of high protein, leucine, fish oil, vitamin D, galacto-oligosaccharides, and fructo-oligosaccharides on the development and progression of cachexia in an orthotopic lung cancer mouse model.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>Eleven-week-old male 129S2/Sv mice were orthotopically implanted with 344P lung epithelial tumour cells or vehicle (control). Seven days post-implantation tumour-bearing (TB) mice were allocated to either intervention- or isocaloric control diet. Cachexia was defined as 5 days of consecutive body weight loss, after which mice were euthanized for tissue analyses.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>TB mice developed cachexia accompanied by significant loss of skeletal muscle mass and epididymal fat mass compared with sham operated mice. The cachectic endpoint was significantly delayed (46.0 ± 15.2 vs. 34.7 ± 11.4 days), and the amount (−1.57 ± 0.62 vs. −2.13 ± 0.57 g) and progression (−0.26 ± 0.14 vs. −0.39 ± 0.11 g/day) of body weight loss were significantly reduced by the intervention compared with control diet. 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引用次数: 0
摘要
背景:恶病质是一种在非小细胞肺癌患者中发病率很高的综合征,会损害患者的生活质量,降低患者对癌症治疗的耐受性和反应性,从而导致生存率下降。最佳营养护理是治疗恶病质的关键,也是多模式疗法的推荐基石。在此,我们研究了由高蛋白、亮氨酸、鱼油、维生素 D、半乳糖寡糖和果糖寡糖的特定组合组成的干预饮食对正位肺癌小鼠模型中恶病质的发生和发展的治疗效果:11周大的雄性129S2/Sv小鼠被正位植入344P肺上皮肿瘤细胞或载体(对照组)。植入后七天,肿瘤携带(TB)小鼠被分配到干预饮食或等热量对照饮食中。连续5天体重下降即为恶病质,之后小鼠被安乐死以进行组织分析:结果:与假手术小鼠相比,肺结核小鼠出现恶病质,并伴有骨骼肌质量和附睾脂肪质量的显著下降。与对照组相比,干预后小鼠的恶病质终点明显推迟(46.0 ± 15.2 天 vs. 34.7 ± 11.4 天),体重下降的数量(-1.57 ± 0.62 克 vs. -2.13 ± 0.57 克)和进展(-0.26 ± 0.14 克 vs. -0.39 ± 0.11 克/天)明显减少。此外,干预饮食还抑制了骨骼肌中的全身炎症(五肽-2 血浆水平)以及蛋白质分解和蛋白质合成分子标志物的改变,这些都表明结核病小鼠肌肉萎缩的信号:总之,这些数据证明了这种针对恶病质多种成分的多营养素干预方法的潜力,是肺癌治疗不可或缺的一部分。
Targeted nutritional intervention attenuates experimental lung cancer cachexia
Background
Cachexia, a syndrome with high prevalence in non-small cell lung cancer patients, impairs quality of life and reduces tolerance and responsiveness to cancer therapy resulting in decreased survival. Optimal nutritional care is pivotal in the treatment of cachexia and a recommended cornerstone of multimodal therapy. Here, we investigated the therapeutic effect of an intervention diet consisting of a specific combination of high protein, leucine, fish oil, vitamin D, galacto-oligosaccharides, and fructo-oligosaccharides on the development and progression of cachexia in an orthotopic lung cancer mouse model.
Methods
Eleven-week-old male 129S2/Sv mice were orthotopically implanted with 344P lung epithelial tumour cells or vehicle (control). Seven days post-implantation tumour-bearing (TB) mice were allocated to either intervention- or isocaloric control diet. Cachexia was defined as 5 days of consecutive body weight loss, after which mice were euthanized for tissue analyses.
Results
TB mice developed cachexia accompanied by significant loss of skeletal muscle mass and epididymal fat mass compared with sham operated mice. The cachectic endpoint was significantly delayed (46.0 ± 15.2 vs. 34.7 ± 11.4 days), and the amount (−1.57 ± 0.62 vs. −2.13 ± 0.57 g) and progression (−0.26 ± 0.14 vs. −0.39 ± 0.11 g/day) of body weight loss were significantly reduced by the intervention compared with control diet. Moreover, systemic inflammation (pentraxin-2 plasma levels) and alterations in molecular markers for proteolysis and protein synthesis, indicative of muscle atrophy signalling in TB-mice, were suppressed in skeletal muscle by the intervention diet.
Conclusions
Together, these data demonstrate the potential of this multinutrient intervention, targeting multiple components of cachexia, as integral part of lung cancer management.
期刊介绍:
The Journal of Cachexia, Sarcopenia and Muscle is a peer-reviewed international journal dedicated to publishing materials related to cachexia and sarcopenia, as well as body composition and its physiological and pathophysiological changes across the lifespan and in response to various illnesses from all fields of life sciences. The journal aims to provide a reliable resource for professionals interested in related research or involved in the clinical care of affected patients, such as those suffering from AIDS, cancer, chronic heart failure, chronic lung disease, liver cirrhosis, chronic kidney failure, rheumatoid arthritis, or sepsis.