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人类肥大细胞和嗜碱性粒细胞对肌肉松弛剂反应的异质性。

Heterogeneity of human mast cells and basophils in response to muscle relaxants.

作者信息

Stellato C, de Paulis A, Cirillo R, Mastronardi P, Mazzarella B, Marone G

机构信息

Division of Clinical Immunology, Second School of Medicine, University of Naples Federico II, Italy.

出版信息

Anesthesiology. 1991 Jun;74(6):1078-86. doi: 10.1097/00000542-199106000-00016.

Abstract

The authors studied the effects of increasing concentrations 10(-5)-10(-3) M) of four muscle relaxants (succinylcholine, d-tubocurarine, vecuronium, and atracurium) on histamine release from peripheral blood basophils and mast cells isolated from human lung parenchyma, skin tissues, and heart fragments. Basophil granulocytes released less than 5% of their histamine content when incubated with any one of the muscle relaxants tested. In contrast, mast cells showed a significant heterogeneity in response to different muscle relaxants. Succinylcholine did not induce histamine release from any type of mast cell, and only high concentrations of d-tubocurarine (10(-3) M) caused histamine release from skin and lung mast cells. Vecuronium concentration-dependently induced histamine release from skin and lung--but not from heart mast cells--to a maximum of 7.2 +/- 2.1% and 4.9 +/- 1.4%, respectively. Atracurium concentration-dependently caused significant histamine release from skin and lung mast cells to a maximum of 46.2 +/- 15.1% and 30.6 +/- 6.0%, respectively. Atracurium (5 x 10(-5) - 2 x 10(-4) M) also induced histamine release from heart mast cells. The histamine release process from both lung and skin mast cells caused by atracurium and vecuronium was extremely rapid (t1/2 = less than 1 min). The releasing activity of atracurium and vecuronium on lung and skin mast cells was not reduced, and not abolished, by lowering the temperature of the incubation buffer to 22 degrees C and 4 degrees C. Extracellular calcium did not affect the capacity of atracurium and vecuronium to induce histamine release from lung and skin mast cells.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

作者研究了四种肌松药(琥珀酰胆碱、d - 筒箭毒碱、维库溴铵和阿曲库铵)浓度增加(10⁻⁵ - 10⁻³M)时,对从人肺实质、皮肤组织和心脏碎片中分离出的外周血嗜碱性粒细胞和肥大细胞组胺释放的影响。与任何一种受试肌松药孵育时,嗜碱性粒细胞释放的组胺含量不到其组胺总量的5%。相比之下,肥大细胞对不同肌松药的反应存在显著异质性。琥珀酰胆碱不会诱导任何类型的肥大细胞释放组胺,只有高浓度的d - 筒箭毒碱(10⁻³M)会导致皮肤和肺肥大细胞释放组胺。维库溴铵浓度依赖性地诱导皮肤和肺肥大细胞释放组胺——但不诱导心脏肥大细胞释放组胺——释放量分别最高可达7.2±2.1%和4.9±1.4%。阿曲库铵浓度依赖性地导致皮肤和肺肥大细胞显著释放组胺,释放量分别最高可达46.2±15.1%和30.6±6.0%。阿曲库铵(5×10⁻⁵ - 2×10⁻⁴M)也会诱导心脏肥大细胞释放组胺。阿曲库铵和维库溴铵引起的肺和皮肤肥大细胞组胺释放过程极其迅速(t1/2<1分钟)。将孵育缓冲液温度降至22℃和4℃时,阿曲库铵和维库溴铵对肺和皮肤肥大细胞的释放活性并未降低,也未消除。细胞外钙不影响阿曲库铵和维库溴铵诱导肺和皮肤肥大细胞释放组胺的能力。(摘要截选至250字)

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