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两代补充鱼油对Walker 256癌性恶病质诱导的大鼠巨噬细胞功能变化的影响。

Effect of fish oil supplementation for 2 generations on changes in macrophage function induced by Walker 256 cancer cachexia in rats.

作者信息

Folador Alessandra, Hirabara Sandro M, Bonatto Sandro J R, Aikawa Júlia, Yamazaki Ricardo K, Curi Rui, Fernandes Luiz C

机构信息

Department of Physiology and Biophysics, Institute de Biomedical Sciences, University of São Paulo, São Paulo, SP, Brazil.

出版信息

Int J Cancer. 2007 Jan 15;120(2):344-50. doi: 10.1002/ijc.22333.

DOI:10.1002/ijc.22333
PMID:17066422
Abstract

The effect of coconut fat (rich in medium saturated fatty acids) or fish oil (rich in omega-3 polyunsaturated fatty acids) supplementation for 2 generations on tumor growth, cancer cachexia, animal survival and macrophage function was investigated in Walker 256 tumor-bearing rats. Female Wistar rats were supplemented with coconut fat or fish oil prior to mating and then throughout pregnancy and gestation. Both supplementations were daily and orally given at 1 g per kg body weight as a single bolus. Same treatment was performed by the 2 following generations. At 90 days of age, male offspring (50%) from F2 generation were subcutaneously inoculated with 2 x 10(7) Walker 256 tumor cells. At 14 days after tumor implantation, rats not supplemented displayed cancer cachexia characterized by loss of body weight, hypoglycemia, hyperlacticidemia, hypertriglyceridemia, decreased food intake and depletion of glycogen stores in the liver and skeletal muscles. Supplementation with coconut fat did not affect these parameters. However, supplementation with fish oil decreased tumor growth (59%), prevented body weight loss and food intake reduction and attenuated cancer cachexia. In addition, fish oil increased animal survival up to 20 days (from 25% in rats not supplemented to 67% in rats supplemented with fish oil) and improved macrophage function characterized by increased phagocytosis capacity and production of hydrogen peroxide and nitric oxide. These results suggest that fish oil supplementation for 2 generations improves macrophage function in association to reduced tumor growth and attenuated cancer cachexia, maintaining food intake and increasing animal survival.

摘要

在荷Walker 256肿瘤大鼠中,研究了连续两代补充富含中链饱和脂肪酸的椰子油或富含ω-3多不饱和脂肪酸的鱼油对肿瘤生长、癌症恶病质、动物存活及巨噬细胞功能的影响。雌性Wistar大鼠在交配前、整个孕期及哺乳期补充椰子油或鱼油。两种补充剂均每日经口给予,剂量为1 g/kg体重,单次灌胃。随后的两代进行相同处理。F2代90日龄雄性后代(50%)皮下接种2×10(7)个Walker 256肿瘤细胞。肿瘤接种后14天,未补充的大鼠出现癌症恶病质,表现为体重减轻、低血糖、高乳酸血症、高甘油三酯血症、食物摄入量减少以及肝脏和骨骼肌糖原储备耗竭。补充椰子油对这些参数无影响。然而,补充鱼油可使肿瘤生长减缓(59%),防止体重减轻和食物摄入量减少,并减轻癌症恶病质。此外,鱼油可使动物存活期延长20天(未补充大鼠的存活率为25%,补充鱼油大鼠的存活率为67%),并改善巨噬细胞功能,表现为吞噬能力增强以及过氧化氢和一氧化氮生成增加。这些结果表明,连续两代补充鱼油可改善巨噬细胞功能,同时减少肿瘤生长、减轻癌症恶病质,维持食物摄入量并提高动物存活率。

相似文献

1
Effect of fish oil supplementation for 2 generations on changes in macrophage function induced by Walker 256 cancer cachexia in rats.两代补充鱼油对Walker 256癌性恶病质诱导的大鼠巨噬细胞功能变化的影响。
Int J Cancer. 2007 Jan 15;120(2):344-50. doi: 10.1002/ijc.22333.
2
Cancer cachexia and tumor growth reduction in Walker 256 tumor-bearing rats supplemented with N-3 polyunsaturated fatty acids for one generation.连续一代补充 N-3 多不饱和脂肪酸对 Walker 256 荷瘤大鼠癌症恶病质及肿瘤生长的影响
Nutr Cancer. 2003;46(1):52-8. doi: 10.1207/S15327914NC4601_07.
3
Chronic supplementation with shark liver oil for reducing tumor growth and cachexia in walker 256 tumor-bearing rats.长期补充鲨鱼肝油可减少 Walker 256 荷瘤大鼠的肿瘤生长和恶病质。
Nutr Cancer. 2011 Nov;63(8):1307-15. doi: 10.1080/01635581.2011.607540. Epub 2011 Oct 7.
4
Effect of fish oil supplementation for two generations on changes of lymphocyte function induced by Walker 256 cancer cachexia in rats.两代鱼油补充对 Walker 256 癌性恶病质诱导的淋巴细胞功能变化的影响。
Nutr Cancer. 2009;61(5):670-9. doi: 10.1080/01635580902825548.
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Fish oil supplementation in F1 generation associated with naproxen, clenbuterol, and insulin administration reduce tumor growth and cachexia in Walker 256 tumor-bearing rats.在给予萘普生、克伦特罗和胰岛素的情况下,F1代大鼠补充鱼油可减少Walker 256荷瘤大鼠的肿瘤生长和恶病质。
J Nutr Biochem. 2004 Jun;15(6):358-65. doi: 10.1016/j.jnutbio.2004.02.002.
6
Glucose metabolism by lymphocytes, macrophages, and tumor cells from Walker 256 tumor-bearing rats supplemented with fish oil for one generation.用鱼油补充一代的荷Walker 256肿瘤大鼠的淋巴细胞、巨噬细胞和肿瘤细胞的葡萄糖代谢。
Cell Biochem Funct. 2008 Dec;26(8):874-80. doi: 10.1002/cbf.1520.
7
Ratio of n6 to n-3 fatty acids in the diet affects tumor growth and cachexia in Walker 256 tumor-bearing rats.饮食中n6与n-3脂肪酸的比例会影响荷Walker 256肿瘤大鼠的肿瘤生长和恶病质。
Nutr Cancer. 2005;53(2):194-201. doi: 10.1207/s15327914nc5302_8.
8
Fish oil alters T-lymphocyte proliferation and macrophage responses in Walker 256 tumor-bearing rats.鱼油改变Walker 256荷瘤大鼠的T淋巴细胞增殖和巨噬细胞反应。
Nutrition. 2006 Apr;22(4):425-32. doi: 10.1016/j.nut.2005.11.001. Epub 2006 Feb 10.
9
Maternal nutritional supplementation with fish oil and/or leucine improves hepatic function and antioxidant defenses, and minimizes cachexia indexes in Walker-256 tumor-bearing rats offspring.给母鼠补充鱼油和/或亮氨酸可改善肝功能和抗氧化防御能力,并最大限度地减少 Walker-256 肿瘤荷瘤大鼠后代的恶病质指标。
Nutr Res. 2018 Mar;51:29-39. doi: 10.1016/j.nutres.2017.12.003. Epub 2017 Dec 28.
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Lifelong exposure to dietary fish oil alters macrophage responses in Walker 256 tumor-bearing rats.终生摄入膳食鱼油会改变Walker 256荷瘤大鼠的巨噬细胞反应。
Cell Immunol. 2004 Sep-Oct;231(1-2):56-62. doi: 10.1016/j.cellimm.2004.12.001. Epub 2005 Jan 20.

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Nutr Diabetes. 2017 Mar 13;7(3):e245. doi: 10.1038/nutd.2016.47.
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Antitumor and anti-cachectic effects of shark liver oil and fish oil: comparison between independent or associative chronic supplementation in Walker 256 tumor-bearing rats.
鲨鱼肝油和鱼油的抗肿瘤和抗恶病质作用:在 Walker 256 荷瘤大鼠中分别或联合进行慢性补充的比较。
Lipids Health Dis. 2013 Oct 16;12:146. doi: 10.1186/1476-511X-12-146.