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本文引用的文献

1
High affinity dextromethorphan binding sites in guinea pig brain: further characterization and allosteric interactions.豚鼠脑中高亲和力右美沙芬结合位点:进一步的特性表征和变构相互作用
J Pharmacol Exp Ther. 1988 Nov;247(2):424-31.
2
Autoradiographic localization of sigma receptor binding sites in guinea pig and rat central nervous system with (+)3H-3-(3-hydroxyphenyl)-N-(1-propyl)piperidine.用(+)³H-3-(3-羟基苯基)-N-(1-丙基)哌啶对豚鼠和大鼠中枢神经系统中σ受体结合位点进行放射自显影定位。
J Neurosci. 1986 Jun;6(6):1757-70. doi: 10.1523/JNEUROSCI.06-06-01757.1986.
3
1,3-Di(2-[5-3H]tolyl)guanidine: a selective ligand that labels sigma-type receptors for psychotomimetic opiates and antipsychotic drugs.
Proc Natl Acad Sci U S A. 1986 Nov;83(22):8784-8. doi: 10.1073/pnas.83.22.8784.
4
Regulation of sigma-receptors: high- and low-affinity agonist states, GTP shifts, and up-regulation by rimcazole and 1,3-Di(2-tolyl)guanidine.σ受体的调节:高亲和力和低亲和力激动剂状态、GTP 转换以及利莫唑和 1,3 - 二(2 - 甲苯基)胍的上调作用
J Neurochem. 1989 Sep;53(3):779-88. doi: 10.1111/j.1471-4159.1989.tb11773.x.
5
Multiple affinity binding states of the sigma receptor: effect of GTP-binding protein-modifying agents.σ受体的多种亲和结合状态:GTP结合蛋白修饰剂的作用
Mol Pharmacol. 1989 Oct;36(4):512-7.
6
A sigma-like binding site in rat pheochromocytoma (PC12) cells: decreased affinity for (+)-benzomorphans and lower molecular weight suggest a different sigma receptor form from that of guinea pig brain.大鼠嗜铬细胞瘤(PC12)细胞中的一个类西格玛结合位点:对(+)-苯并吗啡烷亲和力降低及分子量较低表明其西格玛受体形式与豚鼠脑不同。
Brain Res. 1990 Sep 17;527(2):244-53. doi: 10.1016/0006-8993(90)91143-5.
7
Sigma receptors: biology and function.
Pharmacol Rev. 1990 Dec;42(4):355-402.
8
Labeling by [3H]1,3-di(2-tolyl)guanidine of two high affinity binding sites in guinea pig brain: evidence for allosteric regulation by calcium channel antagonists and pseudoallosteric modulation by sigma ligands.用[3H]1,3 - 二(2 - 甲苯基)胍标记豚鼠脑中的两个高亲和力结合位点:钙通道拮抗剂的变构调节及西格玛配体的拟变构调节的证据
Mol Pharmacol. 1991 Feb;39(2):222-32.
9
The human sigma site, which resembles that in NCB20 cells, may correspond to a low-affinity site in guinea pig brain.
Neurosci Lett. 1991 Oct 14;131(2):233-6. doi: 10.1016/0304-3940(91)90621-y.
10
[3H]DTG and [3H](+)-3-PPP label pharmacologically distinct sigma binding sites in guinea pig brain membranes.[3H]DTG和[3H](+)-3-PPP标记豚鼠脑膜中药理学性质不同的σ结合位点。
Eur J Pharmacol. 1991 Jan 25;193(1):21-7. doi: 10.1016/0014-2999(91)90195-v.

豚鼠和大鼠脑膜中的多个西格玛结合位点:G蛋白相互作用。

Multiple sigma binding sites in guinea-pig and rat brain membranes: G-protein interactions.

作者信息

Connick J H, Hanlon G, Roberts J, France L, Fox P K, Nicholson C D

机构信息

Department of Pharmacology, Organon Laboratories Limited, Newhouse, Lanarkshire.

出版信息

Br J Pharmacol. 1992 Nov;107(3):726-31. doi: 10.1111/j.1476-5381.1992.tb14514.x.

DOI:10.1111/j.1476-5381.1992.tb14514.x
PMID:1361872
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1907754/
Abstract
  1. Evidence is accumulating for multiple sigma (sigma) sites in the mammalian CNS. 2. We have addressed this problem and have examined sigma site - G-protein coupling in guinea-pig and rat brain membranes. 3. Ditolylorthoguanidine (DTG), (+)-3-(3-hydroxyphenyl)-N-1-(propyl)piperidine (3PPP) and dextromethorphan displaced [3H]-DTG (3.4 nM) with low Hill slopes of 0.5, 0.6 and 0.6, respectively in guinea-pig brain membranes. 4. In the presence of 5'-guanylylimidodiphosphate (Gpp(NH)p; 100 microM), the specific binding of [3H]-DTG was reduced by 36.7%, the Hill slope of 3PPP was increased to near unity, the ability of dextromethorphan to displace DTG was virtually abolished and the Hill slope for DTG remained low (0.7), indicating the presence of at least two binding sites. These data indicate that although Gpp(NH)p removes a dextromethorphan high affinity site, two DTG selective sites remain in the presence of Gpp(NH)p. 5. The present study suggests that DTG binds to at least three sites in guinea-pig brain membranes, at least one of which is G-protein linked. 6. In rat brain membranes, DTG displaced itself (3.4 nM) with a Hill slope near 1. 3PPP displacement of [3H]-DTG was comparable with the guinea-pig (Hill slope 0.5) and displaced from more than 1 site. Dextromethorphan did not displace [3H]-DTG at concentrations below 10 microM. 7. The heterogeneity of sigma sites appears to be less in rat than in guinea-pig brain membranes.
摘要
  1. 哺乳动物中枢神经系统中存在多个σ位点的证据正在不断积累。2. 我们已经着手解决这个问题,并研究了豚鼠和大鼠脑膜中σ位点与G蛋白的偶联。3. 在豚鼠脑膜中,二邻甲苯基胍(DTG)、(+)-3-(3-羟苯基)-N-1-(丙基)哌啶(3PPP)和右美沙芬分别以0.5、0.6和0.6的低希尔系数取代[3H]-DTG(3.4 nM)。4. 在5'-鸟苷酰亚胺二磷酸(Gpp(NH)p;100μM)存在的情况下,[3H]-DTG的特异性结合降低了36.7%,3PPP的希尔系数增加到接近1,右美沙芬取代DTG的能力几乎完全丧失,而DTG的希尔系数仍然很低(0.7),这表明至少存在两个结合位点。这些数据表明,尽管Gpp(NH)p去除了右美沙芬的高亲和力位点,但在Gpp(NH)p存在的情况下,仍存在两个DTG选择性位点。5. 本研究表明,DTG在豚鼠脑膜中至少与三个位点结合,其中至少一个位点与G蛋白相连。6. 在大鼠脑膜中,DTG以接近1的希尔系数取代自身(3.4 nM)。3PPP对[3H]-DTG的取代与豚鼠相当(希尔系数0.5),且从多个位点取代。在浓度低于10μM时,右美沙芬不能取代[3H]-DTG。7. σ位点的异质性在大鼠脑膜中似乎比在豚鼠脑膜中要小。