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某些多胺刺激腹膜和胸膜肥大细胞时,纯化介质对其敏感性和最大反应的影响及差异。

Difference in, and influence of the purification medium on, sensitivity and maximum response of peritoneal and pleural mast cells stimulated by certain polyamines.

作者信息

Botana L M, Espinosa J, Eleno N, Segura C, Fernández-Otero P

出版信息

Agents Actions. 1985 Jul;16(5):342-5. doi: 10.1007/BF01982870.

DOI:10.1007/BF01982870
PMID:2413740
Abstract

The actions of the polyamines compound 48/80, poly-l-lysine and polymyxin B on rat pleural and peritoneal mast cell secretion have been studied. Unpurified pleural mast cells released more histamine than peritoneal mast cells when stimulated by submaximal concentrations of compound 48/80 and poly-l-lysine, but the same profile of response was observed with polymyxin B in both populations. Dose-response studies of peritoneal and pleural mast cells purified with Percoll and Ficoll and stimulated by polymyxin B showed a decreased sensitivity and decreased maximum response of peritoneal cells when Percoll was used. The maximal response of pleural cells and the sensitivity of peritoneal cells were affected only slightly by Ficoll.

摘要

已对多胺化合物48/80、聚-L-赖氨酸和多粘菌素B对大鼠胸膜和腹膜肥大细胞分泌的作用进行了研究。当用次最大浓度的化合物48/80和聚-L-赖氨酸刺激时,未纯化的胸膜肥大细胞比腹膜肥大细胞释放更多的组胺,但在两个细胞群体中,多粘菌素B刺激时观察到相同的反应模式。用Percoll和Ficoll纯化并用多粘菌素B刺激的腹膜和胸膜肥大细胞的剂量反应研究表明,当使用Percoll时,腹膜细胞的敏感性降低,最大反应降低。Ficoll对胸膜细胞的最大反应和腹膜细胞的敏感性影响较小。

相似文献

1
Difference in, and influence of the purification medium on, sensitivity and maximum response of peritoneal and pleural mast cells stimulated by certain polyamines.某些多胺刺激腹膜和胸膜肥大细胞时,纯化介质对其敏感性和最大反应的影响及差异。
Agents Actions. 1985 Jul;16(5):342-5. doi: 10.1007/BF01982870.
2
Rat pleural and peritoneal mast cells stimulated at different cellular levels: difference in and influence of purification media.在不同细胞水平刺激的大鼠胸膜和腹膜肥大细胞:纯化介质的差异及影响
Int Arch Allergy Immunol. 1993;100(3):234-9. doi: 10.1159/000236417.
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[Isolation of mastocytes from rat peritoneal fluid using continuous Ficoll gradients].[利用连续Ficoll梯度从大鼠腹腔液中分离肥大细胞]
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引用本文的文献

1
Nonimmunological release of histamine from rat mast cells elicited by antineoplastic agents: effect of drug combinations.抗肿瘤药物引发大鼠肥大细胞组胺的非免疫性释放:药物组合的影响
Cancer Chemother Pharmacol. 1992;30(6):487-90. doi: 10.1007/BF00685603.
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Non-immunological release of histamine from rat mast cells elicited by antineoplastic agents.抗肿瘤药物引发大鼠肥大细胞组胺的非免疫性释放。
Cancer Chemother Pharmacol. 1992;29(6):495-8. doi: 10.1007/BF00684855.

本文引用的文献

1
Isolation of rat peritoneal mast cells by centrifugation on density gradients of Percoll.通过在Percoll密度梯度上离心分离大鼠腹膜肥大细胞。
J Immunol Methods. 1980;39(1-2):135-45. doi: 10.1016/0022-1759(80)90302-6.
2
Some studies on the release of histamine from mast cells treated with polymyxin.关于用多粘菌素处理肥大细胞后组胺释放的一些研究。
Agents Actions. 1984 Apr;14(3-4):379-85. doi: 10.1007/BF01973833.
3
[Secretory activity of mast cells in the presence of cholinergic agonists].[胆碱能激动剂存在下肥大细胞的分泌活性]
Rev Esp Fisiol. 1983 Dec;39(4):441-5.
4
Mast cell heterogeneity.肥大细胞异质性
Monogr Allergy. 1983;18:124-8.
5
Agents that release histamine from mast cells.可从肥大细胞释放组胺的介质。
Annu Rev Pharmacol Toxicol. 1983;23:331-51. doi: 10.1146/annurev.pa.23.040183.001555.
6
Competitive inhibition of 48/80-induced histamine release by benzalkonium chloride and its analogs and the polyamine receptor in mast cells.苯扎氯铵及其类似物对48/80诱导的肥大细胞组胺释放的竞争性抑制作用以及多胺受体的作用
J Pharmacol Exp Ther. 1982 Sep;222(3):652-7.
7
A comparative study of histamine secretion from rat peritoneal and pleural mast cells.大鼠腹膜肥大细胞和胸膜肥大细胞组胺分泌的比较研究。
Agents Actions. 1982 Apr;12(1-2):186-8. doi: 10.1007/BF01965141.
8
Evidence against a role of cyclic nucleotides in the regulation of anaphylactic histamine release in isolated rat mast cells.关于环核苷酸在离体大鼠肥大细胞过敏性组胺释放调节中作用的反对证据。
Acta Physiol Scand. 1981 May;112(1):47-56. doi: 10.1111/j.1748-1716.1981.tb06781.x.
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A comparison of the histamine-releasing properties of rat pleural and peritoneal mast cells.大鼠胸膜和腹膜肥大细胞组胺释放特性的比较。
Immunology. 1980 Oct;41(2):271-8.
10
Release of histamine from rat mast cells: a comparison of the effects of 48-80 and two antigen systems.大鼠肥大细胞组胺的释放:48-80与两种抗原系统作用的比较
Fed Proc. 1969 Sep-Oct;28(5):1716-20.