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巯基试剂N-乙基马来酰亚胺对利血平与嗜铬粒细胞膜中儿茶酚胺转运体结合的影响。

Effects of the sulfhydryl reagent N-ethylmaleimide on reserpine binding to the catecholamine transporter in chromaffin granule membranes.

作者信息

Deupree J D, Hitchcock J J

机构信息

Department of Pharmacology, University of Nebraska College of Medicine, Omaha 68105.

出版信息

Cell Mol Neurobiol. 1988 Jun;8(2):217-24. doi: 10.1007/BF00711247.

Abstract
  1. Catecholamines are transported into chromaffin granules via a carrier-mediated, active-transport process which is inhibited by micromolar concentrations of the sulfhydryl reagent, N-ethylmaleimide (NEM). Reserpine is a very potent, competitive inhibitor of the catecholamine transporter and can be used to investigate the characteristics of the catecholamine transporter. 2. The purpose of this study was to determine whether [3H]reserpine binding to the catecholamine transporter present in chromaffin granule membranes isolated from bovine adrenal glands was also inhibited by NEM and, if so, whether this was a direct or an indirect effect of NEM on the catecholamine transporter. 3. Both [3H]norepinephrine transport into and [3H]reserpine binding to the chromaffin granule ghosts isolated from bovine adrenal glands are inhibited by NEM, with IC50 values of 0.63 +/- 0.02 and 2.8 +/- 0.66 microM, respectively. 4. Mg and ATP protected both the [3H]norepinephrine transport into the ghosts and the [3H]reserpine binding to the transporter from inhibition by NEM, shifting the IC50 values to 260 +/- 43 and 120 +/- 29 microM, respectively. 5. NEM inhibition of the catecholamine transport and reserpine binding appears to be due to an action on the proton translocator associated with the Mg ATPase enzyme rather than a direct action on the catecholamine transporter since (a) the concentration of NEM required to inhibit formation of a membrane potential is similar to that required to inhibit [3H]norepinephrine transport into and [3H]reserpine binding to the ghosts and (b) Mg and ATP protected the proton translocation and [3H]norepinephrine transport into the ghosts, and [3H]reserpine binding to the ghosts, from inhibition by NEM.(ABSTRACT TRUNCATED AT 250 WORDS)
摘要
  1. 儿茶酚胺通过一种载体介导的主动转运过程被转运到嗜铬颗粒中,该过程会被微摩尔浓度的巯基试剂N - 乙基马来酰亚胺(NEM)抑制。利血平是一种非常有效的儿茶酚胺转运体竞争性抑制剂,可用于研究儿茶酚胺转运体的特性。2. 本研究的目的是确定从牛肾上腺分离的嗜铬颗粒膜中存在的儿茶酚胺转运体与[3H]利血平的结合是否也会被NEM抑制,如果是,这是NEM对儿茶酚胺转运体的直接作用还是间接作用。3. NEM抑制了从牛肾上腺分离的嗜铬颗粒膜泡对[3H]去甲肾上腺素的摄取以及[3H]利血平与膜泡的结合,IC50值分别为0.63±0.02和2.8±0.66微摩尔。4. 镁离子和ATP保护了膜泡对[3H]去甲肾上腺素的摄取以及[3H]利血平与转运体的结合不被NEM抑制,将IC50值分别转移至260±43和120±29微摩尔。5. NEM对儿茶酚胺转运和利血平结合的抑制作用似乎是由于其对与镁ATP酶相关的质子转运体的作用而非对儿茶酚胺转运体的直接作用,因为(a)抑制膜电位形成所需的NEM浓度与抑制[3H]去甲肾上腺素摄取以及[3H]利血平与膜泡结合所需的浓度相似,并且(b)镁离子和ATP保护了质子转运以及[3H]去甲肾上腺素摄取和[3H]利血平与膜泡的结合不被NEM抑制。(摘要截选至250字)

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