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[3-羟基-3-甲基戊二酰辅酶A还原酶抑制剂普伐他汀和辛伐他汀对造血祖细胞集落形成的影响]

[Effect of the inhibitors of 3-hydroxy-3-methylglutaryl coenzyme-A reductase, pravastatin and simvastatin, on colony formation by hematopoietic progenitor cells].

作者信息

Kunitama M, Komatsu N, Miura Y

机构信息

Department of Medicine, Jichi Medical School.

出版信息

Rinsho Ketsueki. 1996 Nov;37(11):1314-7.

PMID:8960668
Abstract

The inhibitors of 3-hydroxy-3-methylglutaryl-coenzyme-A (HMG-CoA) reductase, pravastatin and simvastatin, are widely used clinically as anti-hypercholesterolemic drugs. To determine whether these drugs affect hematopoiesis, we examined the effect of the drugs on colony formation by human bone marrow cells. Simvastatin strongly inhibited both erythroid and granulocyte-macrophage colony formation by total or CD34-positive bone marrow cells at the concentration of 10 microM, which is about 100-1,000 fold higher than the pharmacologically effective level. On the other hand, the inhibitory effect of pravastatin was much weaker than that of simvastatin. These findings show that these drugs, especially pravastatin have little effect on hematopoiesis.

摘要

3-羟基-3-甲基戊二酰辅酶A(HMG-CoA)还原酶抑制剂普伐他汀和辛伐他汀在临床上被广泛用作抗高胆固醇血症药物。为了确定这些药物是否影响造血作用,我们检测了它们对人骨髓细胞集落形成的影响。辛伐他汀在10微摩尔浓度时强烈抑制总骨髓细胞或CD34阳性骨髓细胞的红系和粒-巨噬细胞集落形成,该浓度比药理有效水平高约100-1000倍。另一方面,普伐他汀的抑制作用比辛伐他汀弱得多。这些发现表明这些药物,尤其是普伐他汀对造血作用几乎没有影响。

相似文献

1
[Effect of the inhibitors of 3-hydroxy-3-methylglutaryl coenzyme-A reductase, pravastatin and simvastatin, on colony formation by hematopoietic progenitor cells].[3-羟基-3-甲基戊二酰辅酶A还原酶抑制剂普伐他汀和辛伐他汀对造血祖细胞集落形成的影响]
Rinsho Ketsueki. 1996 Nov;37(11):1314-7.
2
A comparison of the effect of the 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors simvastatin, lovastatin and pravastatin on leukaemic and normal bone marrow progenitors.3-羟基-3-甲基戊二酰辅酶A(HMG-CoA)还原酶抑制剂辛伐他汀、洛伐他汀和普伐他汀对白血病和正常骨髓祖细胞作用的比较。
Leuk Lymphoma. 1997 Feb;24(5-6):533-7. doi: 10.3109/10428199709055590.
3
Pharmacological profile of a novel synthetic inhibitor of 3-hydroxy-3-methylglutaryl-coenzyme A reductase.一种新型3-羟基-3-甲基戊二酰辅酶A还原酶合成抑制剂的药理学特性
Arzneimittelforschung. 1997 Aug;47(8):904-9.
4
Effects of different inhibitors of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase, pravastatin sodium and simvastatin, on sterol synthesis and immunological functions in human lymphocytes in vitro.3-羟基-3-甲基戊二酰辅酶A(HMG-CoA)还原酶的不同抑制剂普伐他汀钠和辛伐他汀对人淋巴细胞体外胆固醇合成及免疫功能的影响。
Immunopharmacology. 1996 Aug;34(1):51-61. doi: 10.1016/0162-3109(96)00108-7.
5
Inhibition of rat brain prostaglandin D synthase by 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors.3-羟基-3-甲基戊二酰辅酶A还原酶抑制剂对大鼠脑前列腺素D合酶的抑制作用
Biochem Int. 1990 Nov;22(4):601-5.
6
Potential risk of myopathy by HMG-CoA reductase inhibitors: a comparison of pravastatin and simvastatin effects on membrane electrical properties of rat skeletal muscle fibers.HMG-CoA还原酶抑制剂引发肌病的潜在风险:普伐他汀与辛伐他汀对大鼠骨骼肌纤维膜电特性影响的比较
J Pharmacol Exp Ther. 1995 Dec;275(3):1490-6.
7
Pravastatin inhibited the cholesterol synthesis in human hepatoma cell line Hep G2 less than simvastatin and lovastatin, which is reflected in the upregulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase and squalene synthase.普伐他汀对人肝癌细胞系Hep G2胆固醇合成的抑制作用小于辛伐他汀和洛伐他汀,这体现在3-羟基-3-甲基戊二酰辅酶A还原酶和角鲨烯合酶的上调。
Biochem Pharmacol. 1993 Jun 9;45(11):2203-8. doi: 10.1016/0006-2952(93)90190-8.
8
Transport mechanism of 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors at the blood-brain barrier.3-羟基-3-甲基戊二酰辅酶A还原酶抑制剂在血脑屏障的转运机制。
J Pharmacol Exp Ther. 1993 Dec;267(3):1085-90.
9
Determination of the HMG-CoA reductase inhibitors simvastatin, lovastatin, and pravastatin in plasma by gas chromatography/chemical ionization mass spectrometry.采用气相色谱/化学电离质谱法测定血浆中HMG-CoA还原酶抑制剂辛伐他汀、洛伐他汀和普伐他汀。
Biol Mass Spectrom. 1993 Jan;22(1):1-8. doi: 10.1002/bms.1200220102.
10
Compactin and simvastatin, but not pravastatin, induce bone morphogenetic protein-2 in human osteosarcoma cells.洛伐他汀和辛伐他汀可诱导人骨肉瘤细胞产生骨形态发生蛋白-2,但普伐他汀则不能。
Biochem Biophys Res Commun. 2000 May 19;271(3):688-92. doi: 10.1006/bbrc.2000.2697.

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Clin Drug Investig. 1998;16(2):172-4. doi: 10.2165/00044011-199816020-00011.