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1
In vivo gene therapy for hyperlipidemia: phenotypic correction in Watanabe rabbits by hepatic delivery of the rabbit LDL receptor gene.高脂血症的体内基因治疗:通过肝脏递送兔低密度脂蛋白受体基因对渡边兔进行表型矫正
J Clin Invest. 1995 Feb;95(2):768-73. doi: 10.1172/JCI117725.
2
High dose of fluvastatin sodium (XU62-320), a new inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A reductase, lowers plasma cholesterol levels in homozygous Watanabe-heritable hyperlipidemic rabbits.高剂量的氟伐他汀钠(XU62 - 320),一种新型的3 - 羟基 - 3 - 甲基戊二酰辅酶A还原酶抑制剂,可降低纯合子渡边遗传性高脂血症兔的血浆胆固醇水平。
Biochim Biophys Acta. 1995 Oct 26;1259(1):99-104. doi: 10.1016/0005-2760(95)00155-6.
3
Long-term lowering of plasma cholesterol levels in LDL-receptor-deficient WHHL rabbits by gene therapy.
Mol Ther. 2004 Apr;9(4):548-56. doi: 10.1016/j.ymthe.2004.01.015.
4
Familial hypercholesterolemia: molecular, biochemical, and clinical characterization of a French-Canadian pediatric population.家族性高胆固醇血症:法裔加拿大儿科人群的分子、生化及临床特征
Pediatrics. 1995 Aug;96(2 Pt 1):239-46.
5
Retroviral vector-mediated in vivo expression of low-density-lipoprotein receptors in the Watanabe heritable hyperlipidemic rabbit.逆转录病毒载体介导低密度脂蛋白受体在渡边遗传性高脂血症兔体内的表达
Somat Cell Mol Genet. 1991 May;17(3):287-301. doi: 10.1007/BF01232823.
6
Apolipoprotein A-I and lecithin:cholesterol acyltransferase transfer induce cholesterol unloading in complex atherosclerotic lesions.载脂蛋白 A-I 和卵磷脂胆固醇酰基转移酶转移诱导复杂动脉粥样硬化病变中的胆固醇卸载。
Gene Ther. 2009 Jun;16(6):757-65. doi: 10.1038/gt.2009.8. Epub 2009 Feb 26.
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Adenoviral delivery of low-density lipoprotein receptors to hyperlipidemic rabbits: receptor expression modulates high-density lipoproteins.向高脂血症兔腺病毒介导递送低密度脂蛋白受体:受体表达调节高密度脂蛋白。
Metabolism. 1996 Dec;45(12):1447-57. doi: 10.1016/s0026-0495(96)90172-9.
8
Enhanced plasma cholesterol lowering effect of retrovirus-mediated LDL receptor gene transfer to WHHL rabbit liver after improved surgical technique and stimulation of hepatocyte proliferation by combined partial liver resection and thymidine kinase--ganciclovir treatment.在改进手术技术并通过联合部分肝切除术和胸苷激酶-更昔洛韦治疗刺激肝细胞增殖后,逆转录病毒介导的低密度脂蛋白受体基因转移至WHHL兔肝脏可增强血浆胆固醇降低效果。
Gene Ther. 1999 Jan;6(1):34-41. doi: 10.1038/sj.gt.3300796.
9
Unexpected inhibition of cholesterol 7 alpha-hydroxylase by cholesterol in New Zealand white and Watanabe heritable hyperlipidemic rabbits.胆固醇对新西兰白兔和渡边遗传性高脂血症兔胆固醇7α-羟化酶的意外抑制作用
J Clin Invest. 1995 Apr;95(4):1497-504. doi: 10.1172/JCI117821.
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Temporary amelioration of hyperlipidemia in low density lipoprotein receptor-deficient rabbits transplanted with genetically modified hepatocytes.移植转基因肝细胞的低密度脂蛋白受体缺陷兔高脂血症的短暂改善
Proc Natl Acad Sci U S A. 1990 Nov;87(21):8437-41. doi: 10.1073/pnas.87.21.8437.

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Improved extracellular vesicle-based mRNA delivery for familial hypercholesterolemia treatment.改善基于细胞外囊泡的 mRNA 递送来治疗家族性高胆固醇血症。
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Exosome-based gene therapy for familial hypercholesterolemia in a mouse model.基于外泌体的家族性高胆固醇血症基因治疗在小鼠模型中的研究。
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Episomal Nonviral Gene Therapy Vectors Slow Progression of Atherosclerosis in a Model of Familial Hypercholesterolemia.游离型非病毒基因治疗载体减缓家族性高胆固醇血症模型中动脉粥样硬化的进展。
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Restoration of Physiologically Responsive Low-Density Lipoprotein Receptor-Mediated Endocytosis in Genetically Deficient Induced Pluripotent Stem Cells.在基因缺陷的诱导多能干细胞中恢复生理反应性低密度脂蛋白受体介导的内吞作用
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6
LDLR-Gene therapy for familial hypercholesterolaemia: problems, progress, and perspectives.家族性高胆固醇血症的低密度脂蛋白受体基因治疗:问题、进展与展望
Int Arch Med. 2010 Dec 13;3:36. doi: 10.1186/1755-7682-3-36.
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Long-term physiologically regulated expression of the low-density lipoprotein receptor in vivo using genomic DNA mini-gene constructs.利用基因组 DNA 小基因构建物在体内长期生理性调节低密度脂蛋白受体的表达。
Mol Ther. 2010 Feb;18(2):317-26. doi: 10.1038/mt.2009.249. Epub 2009 Oct 27.
8
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A bovine papillomavirus-1 based vector restores the function of the low-density lipoprotein receptor in the receptor-deficient CHO-ldlA7 cell line.一种基于牛乳头瘤病毒1型的载体可恢复受体缺陷型CHO-ldlA7细胞系中低密度脂蛋白受体的功能。
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10
Gene therapy to promote thromboresistance: local overexpression of tissue plasminogen activator to prevent arterial thrombosis in an in vivo rabbit model.促进抗血栓形成的基因治疗:组织纤溶酶原激活剂在体内兔模型中的局部过表达以预防动脉血栓形成。
Proc Natl Acad Sci U S A. 1999 Feb 2;96(3):1065-70. doi: 10.1073/pnas.96.3.1065.

本文引用的文献

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Competitive inhibition of 3-hydroxy-3-methylglutaryl coenzyme A reductase by ML-236A and ML-236B fungal metabolites, having hypocholesterolemic activity.ML-236A和ML-236B真菌代谢产物对3-羟基-3-甲基戊二酰辅酶A还原酶的竞争性抑制作用,具有降胆固醇活性。
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CHOLESTYRAMINE RESIN THERAPY FOR HYPERCHOLESTEREMIA: CLINICAL AND METABOLIC STUDIES.考来烯胺树脂治疗高胆固醇血症:临床与代谢研究
JAMA. 1965 Apr 26;192:289-93. doi: 10.1001/jama.1965.03080170017004.
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THE INHERITANCE OF ESSENTIAL FAMILIAL HYPERCHOLESTEROLEMIA.家族性高胆固醇血症的遗传
Am J Med. 1964 Sep;37:402-7. doi: 10.1016/0002-9343(64)90196-2.
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Familial hypercholesterolemia, xanthomatosis and coronary heart disease.家族性高胆固醇血症、黄瘤病与冠心病。
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Assessment of recombinant adenoviral vectors for hepatic gene therapy.用于肝脏基因治疗的重组腺病毒载体评估
Hum Gene Ther. 1993 Aug;4(4):403-9. doi: 10.1089/hum.1993.4.4-403.
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Hepatic gene therapy: adenovirus enhancement of receptor-mediated gene delivery and expression in primary hepatocytes.肝脏基因治疗:腺病毒增强受体介导的基因递送及在原代肝细胞中的表达
Proc Natl Acad Sci U S A. 1993 Mar 15;90(6):2122-6. doi: 10.1073/pnas.90.6.2122.
7
Hypercholesterolemia in low density lipoprotein receptor knockout mice and its reversal by adenovirus-mediated gene delivery.低密度脂蛋白受体基因敲除小鼠的高胆固醇血症及其通过腺病毒介导的基因递送的逆转。
J Clin Invest. 1993 Aug;92(2):883-93. doi: 10.1172/JCI116663.
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Long-term correction of mouse dystrophic degeneration by adenovirus-mediated transfer of a minidystrophin gene.通过腺病毒介导的小肌营养不良蛋白基因转移对小鼠营养不良性变性进行长期矫正。
Nat Genet. 1993 Oct;5(2):130-4. doi: 10.1038/ng1093-130.
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In vivo correction of low density lipoprotein receptor deficiency in the Watanabe heritable hyperlipidemic rabbit with recombinant adenoviruses.
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10
In vivo hepatic gene therapy: complete albeit transient correction of factor IX deficiency in hemophilia B dogs.体内肝脏基因治疗:血友病B犬中因子IX缺乏症的完全纠正,尽管是短暂的。
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高脂血症的体内基因治疗:通过肝脏递送兔低密度脂蛋白受体基因对渡边兔进行表型矫正

In vivo gene therapy for hyperlipidemia: phenotypic correction in Watanabe rabbits by hepatic delivery of the rabbit LDL receptor gene.

作者信息

Li J, Fang B, Eisensmith R C, Li X H, Nasonkin I, Lin-Lee Y C, Mims M P, Hughes A, Montgomery C D, Roberts J D

机构信息

Department of Cell Biology, Baylor College of Medicine, Houston, Texas 77030.

出版信息

J Clin Invest. 1995 Feb;95(2):768-73. doi: 10.1172/JCI117725.

DOI:10.1172/JCI117725
PMID:7860759
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC295550/
Abstract

Elevations of plasma total or LDL cholesterol are major risk factors for cardiovascular disease. Efforts directed at preventing and treating cardiovascular disease have often focused on reducing the levels of these substances in the blood. The Watanabe Heritable Hyperlipidemic Rabbit, which has exceedingly high plasma cholesterol levels resulting from an LDL receptor deficiency, provides an excellent animal model for testing new treatments. A recombinant adenoviral vector containing the rabbit LDL receptor cDNA was administered to Watanabe rabbits. Plasma total cholesterol levels in the treated animals were reduced from 825.5 +/- 69.8 (mean +/- SD) to 247.3 +/- 61.5 mg/dl 6 d after infusion. These animals also demonstrated a 300-400% increase in plasma levels of HDL cholesterol and apo AI 10 d after treatment. As a result, the LDL:HDL ratio exhibited a dramatic decrease. Because only the rabbit LDL receptor gene was used for treatment, the results strongly suggest that the elevations of plasma HDL cholesterol and apo AI were secondary to a reduction in plasma total cholesterol in the treated animals. These results suggest an inverse relationship between plasma LDL and HDL cholesterol levels and imply that reduction of LDL cholesterol levels may have a beneficial effect on plasma HDL cholesterol.

摘要

血浆总胆固醇或低密度脂蛋白胆固醇升高是心血管疾病的主要危险因素。预防和治疗心血管疾病的努力通常集中在降低血液中这些物质的水平上。渡边遗传性高脂血症兔由于低密度脂蛋白受体缺乏而具有极高的血浆胆固醇水平,为测试新疗法提供了一个极好的动物模型。将含有兔低密度脂蛋白受体cDNA的重组腺病毒载体给予渡边兔。输注6天后,治疗动物的血浆总胆固醇水平从825.5±69.8(平均值±标准差)降至247.3±61.5mg/dl。治疗10天后,这些动物的血浆高密度脂蛋白胆固醇和载脂蛋白AI水平也提高了300 - 400%。结果,低密度脂蛋白:高密度脂蛋白比值显著降低。由于仅使用兔低密度脂蛋白受体基因进行治疗,结果强烈表明治疗动物血浆高密度脂蛋白胆固醇和载脂蛋白AI的升高是血浆总胆固醇降低的继发结果。这些结果表明血浆低密度脂蛋白和高密度脂蛋白胆固醇水平之间存在负相关关系,并暗示降低低密度脂蛋白胆固醇水平可能对血浆高密度脂蛋白胆固醇有有益影响。