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丹曲林对大鼠肺泡巨噬细胞中L-精氨酸转运和一氧化氮合酶的抑制作用。

The inhibition by dantrolene of L-arginine transport and nitric oxide synthase in rat alveolar macrophages.

作者信息

Chou T C, Li C Y, Wu C C, Yen M H, Ding Y A

机构信息

Graduate Institute of Medical Sciences and Department of Medical Research, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan, Republic of China.

出版信息

Anesth Analg. 1998 May;86(5):1065-9. doi: 10.1097/00000539-199805000-00031.

Abstract

UNLABELLED

Dantrolene decreases the free cytosolic Ca2+ level via inhibition of calcium release from the sacroplasmic reticulum. However, the effect of dantrolene on L-arginine transport and nitric oxide synthase (NOS) activity is still unknown. In this study, we examined the effects of dantrolene on L-arginine transport and activity of inducible nitric oxide synthase (iNOS) induced by lipopolysaccharide (LPS) and interferon gamma (IFN-gamma) in rat alveolar macrophages. Incubation of cells with LPS (1 microg/mL) and IFN-gamma (100 u/mL) for 24 h resulted in significant increases in nitrite production and L-arginine transport. In the presence of dantrolene (100 microM) or inhibitors of NOS, such as aminoguanidine (100 microM), N(G)-monomethyl-L-arginine (100 microM), the nitrite production and L-arginine transport were significantly inhibited compared with that in the LPS + IFN-gamma group. Furthermore, the results of kinetic analysis indicate that the suppression of L-arginine transport by dantrolene was caused by selective decrease of the velocity of transport (Vmax) without affecting the affinity (Km) for L-arginine. In addition, dantrolene also attenuated the activity of iNOS in a dose-dependent manner. We conclude that the mechanisms by which dantrolene attenuated NO synthesis may be associated with the inhibition of availability of L-arginine by reducing the affinity for L-arginine, accompanied by a parallel decrease of the activity of iNOS.

IMPLICATIONS

In this study, we demonstrated that dantrolene, a drug that reduces the intracellular Ca2+ level, can inhibit L-arginine availability and inducible nitric oxide synthase activity in macrophages. Our finding may provide a novel therapeutic approach using dantrolene to prevent hypotension associated with an activation of inducible nitric oxide synthase in endotoxemia.

摘要

未标记

丹曲林通过抑制肌浆网释放钙来降低游离胞浆钙离子水平。然而,丹曲林对L-精氨酸转运和一氧化氮合酶(NOS)活性的影响仍不清楚。在本研究中,我们检测了丹曲林对脂多糖(LPS)和干扰素γ(IFN-γ)诱导的大鼠肺泡巨噬细胞中L-精氨酸转运和诱导型一氧化氮合酶(iNOS)活性的影响。用LPS(1微克/毫升)和IFN-γ(100单位/毫升)孵育细胞24小时导致亚硝酸盐生成和L-精氨酸转运显著增加。与LPS + IFN-γ组相比,在丹曲林(100微摩尔)或NOS抑制剂如氨基胍(100微摩尔)、N(G)-单甲基-L-精氨酸(100微摩尔)存在的情况下,亚硝酸盐生成和L-精氨酸转运受到显著抑制。此外,动力学分析结果表明,丹曲林对L-精氨酸转运的抑制是由于转运速度(Vmax)选择性降低而不影响对L-精氨酸的亲和力(Km)。此外,丹曲林还以剂量依赖的方式减弱了iNOS的活性。我们得出结论,丹曲林减弱NO合成的机制可能与通过降低对L-精氨酸的亲和力来抑制L-精氨酸的可用性有关,同时iNOS活性平行降低。

启示

在本研究中,我们证明了丹曲林这种降低细胞内钙离子水平的药物,可以抑制巨噬细胞中L-精氨酸的可用性和诱导型一氧化氮合酶活性。我们的发现可能为使用丹曲林预防内毒素血症中与诱导型一氧化氮合酶激活相关的低血压提供一种新的治疗方法。

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