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1
Inflammatory mediators and modulators release in organ culture from rabbit skin lesions produced in vivo by sulfur mustard. II. Evans blue dye experiments that determined the rates of entry and turnover of serum protein in developing and healing lesions.炎症介质和调节剂在体内由芥子气所致兔皮肤损伤的器官培养中的释放。II. 伊文思蓝染料实验测定血清蛋白在正在形成和愈合损伤中的进入和周转速率。
Am J Pathol. 1985 Oct;121(1):28-38.
2
Inflammatory mediators and modulators released in organ culture from rabbit skin lesions produced in vivo by sulfur mustard. I. Quantitative histopathology; PMN, basophil, and mononuclear cell survival; and unbound (serum) protein content.通过芥子气在体内诱导产生的兔皮肤损伤在器官培养中释放的炎性介质和调节剂。I. 定量组织病理学;中性粒细胞、嗜碱性粒细胞和单核细胞存活情况;以及未结合(血清)蛋白含量。
Am J Pathol. 1985 Oct;121(1):15-27.
3
Inflammatory mediators and modulators released in organ culture from rabbit skin lesions produced in vivo by sulfur mustard. III. Electrophoretic protein fractions, trypsin-inhibitory capacity, alpha 1-proteinase inhibitor, and alpha 1- and alpha 2-macroglobulin proteinase inhibitors of culture fluids and serum.在体内由硫芥产生的兔皮肤损伤的器官培养物中释放的炎性介质和调节剂。III. 培养液和血清的电泳蛋白组分、胰蛋白酶抑制能力、α1-蛋白酶抑制剂以及α1和α2-巨球蛋白蛋白酶抑制剂
Am J Pathol. 1987 Jan;126(1):148-63.
4
Proteases released in organ culture by acute dermal inflammatory lesions produced in vivo in rabbit skin by sulfur mustard: hydrolysis of synthetic peptide substrates for trypsin-like and chymotrypsin-like enzymes.硫芥在兔皮肤体内产生急性皮肤炎性损伤后,在器官培养中释放的蛋白酶:对胰蛋白酶样和糜蛋白酶样酶的合成肽底物的水解作用
Inflammation. 1988 Aug;12(4):311-34. doi: 10.1007/BF00915768.
5
Chemotactic factors released in culture by intact developing and healing skin lesions produced in rabbits by the irritant sulfur mustard.由刺激性芥子气在兔身上造成的完整的正在发展和愈合的皮肤损伤在培养物中释放的趋化因子。
Inflammation. 1997 Apr;21(2):251-67. doi: 10.1023/a:1027378422627.
6
Cytokine, chemokine, and matrix metalloproteinase response after sulfur mustard injury to weanling pig skin.硫芥损伤断奶仔猪皮肤后细胞因子、趋化因子和基质金属蛋白酶的反应
J Biochem Mol Toxicol. 2002;16(6):263-72. doi: 10.1002/jbt.10050.
7
Pathogenesis of skin lesions caused by sulfur mustard.芥子气所致皮肤损伤的发病机制。
Fundam Appl Toxicol. 1984 Apr;4(2 Pt 2):S71-83. doi: 10.1016/0272-0590(84)90139-8.
8
Extracellular collagenase, proteoglycanase and products of their activity, released in organ culture by intact dermal inflammatory lesions produced by sulfur mustard.细胞外胶原酶、蛋白聚糖酶及其活性产物,由硫芥产生的完整皮肤炎性损伤在器官培养中释放。
J Invest Dermatol. 1990 Dec;95(6):717-26. doi: 10.1111/1523-1747.ep12514523.
9
Ocular injuries following sulfur mustard exposure--pathological mechanism and potential therapy.芥子气暴露后的眼部损伤——病理机制与潜在治疗方法
Toxicology. 2009 Sep 1;263(1):59-69. doi: 10.1016/j.tox.2008.10.026. Epub 2008 Nov 17.
10
Mediators, initiating the inflammatory response, released in organ culture by full-thickness human skin explants exposed to the irritant, sulfur mustard.介质,引发炎症反应,由暴露于刺激性物质芥子气的全层人皮肤外植体在器官培养中释放。
J Invest Dermatol. 1991 Jun;96(6):888-97. doi: 10.1111/1523-1747.ep12475292.

引用本文的文献

1
Skin Models Used to Define Mechanisms of Action of Sulfur Mustard.用于定义硫芥作用机制的皮肤模型。
Disaster Med Public Health Prep. 2023 Oct 18;17:e551. doi: 10.1017/dmp.2023.177.
2
Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.基于基因组学和流行病学的人群结构研究中的全基因组关联分析对白细胞和血小板特征的多民族研究。
BMC Genomics. 2021 Jun 9;22(1):432. doi: 10.1186/s12864-021-07745-5.
3
Albumin as a marker of plasma transudation in experimental skin lesions.白蛋白作为实验性皮肤损伤中血浆渗出的标志物。
Int J Legal Med. 2004 Oct;118(5):282-8. doi: 10.1007/s00414-004-0460-5.
4
Chemotactic factors released in culture by intact developing and healing skin lesions produced in rabbits by the irritant sulfur mustard.由刺激性芥子气在兔身上造成的完整的正在发展和愈合的皮肤损伤在培养物中释放的趋化因子。
Inflammation. 1997 Apr;21(2):251-67. doi: 10.1023/a:1027378422627.
5
The cytokines NAP-1 (IL-8), MCP-1, IL-1 beta, and GRO in rabbit inflammatory skin lesions produced by the chemical irritant sulfur mustard.由化学刺激物芥子气引起的兔炎症性皮肤损伤中的细胞因子NAP-1(白细胞介素-8)、单核细胞趋化蛋白-1、白细胞介素-1β和生长调节致癌基因。
Inflammation. 1996 Jun;20(3):293-318. doi: 10.1007/BF01488205.
6
Inflammatory mediators and modulators released in organ culture from rabbit skin lesions produced in vivo by sulfur mustard. I. Quantitative histopathology; PMN, basophil, and mononuclear cell survival; and unbound (serum) protein content.通过芥子气在体内诱导产生的兔皮肤损伤在器官培养中释放的炎性介质和调节剂。I. 定量组织病理学;中性粒细胞、嗜碱性粒细胞和单核细胞存活情况;以及未结合(血清)蛋白含量。
Am J Pathol. 1985 Oct;121(1):15-27.
7
Proteases released in organ culture by acute dermal inflammatory lesions produced in vivo in rabbit skin by sulfur mustard: hydrolysis of synthetic peptide substrates for trypsin-like and chymotrypsin-like enzymes.硫芥在兔皮肤体内产生急性皮肤炎性损伤后,在器官培养中释放的蛋白酶:对胰蛋白酶样和糜蛋白酶样酶的合成肽底物的水解作用
Inflammation. 1988 Aug;12(4):311-34. doi: 10.1007/BF00915768.
8
Inflammatory mediators and modulators released in organ culture from rabbit skin lesions produced in vivo by sulfur mustard. III. Electrophoretic protein fractions, trypsin-inhibitory capacity, alpha 1-proteinase inhibitor, and alpha 1- and alpha 2-macroglobulin proteinase inhibitors of culture fluids and serum.在体内由硫芥产生的兔皮肤损伤的器官培养物中释放的炎性介质和调节剂。III. 培养液和血清的电泳蛋白组分、胰蛋白酶抑制能力、α1-蛋白酶抑制剂以及α1和α2-巨球蛋白蛋白酶抑制剂
Am J Pathol. 1987 Jan;126(1):148-63.

本文引用的文献

1
Protein inhibitors of proteinases.蛋白酶的蛋白质抑制剂。
Annu Rev Biochem. 1980;49:593-626. doi: 10.1146/annurev.bi.49.070180.003113.
2
Endogenous anti-inflammatory factors.内源性抗炎因子
Biochem Pharmacol. 1984 Jun 1;33(11):1705-14. doi: 10.1016/0006-2952(84)90337-x.
3
Pathogenesis of skin lesions caused by sulfur mustard.芥子气所致皮肤损伤的发病机制。
Fundam Appl Toxicol. 1984 Apr;4(2 Pt 2):S71-83. doi: 10.1016/0272-0590(84)90139-8.
4
Formation of human plasma kinin.人血浆激肽的形成。
N Engl J Med. 1974 Sep 5;291(10):509-15. doi: 10.1056/NEJM197409052911008.
5
Inflammatory mediators and modulators released in organ culture from rabbit skin lesions produced in vivo by sulfur mustard. I. Quantitative histopathology; PMN, basophil, and mononuclear cell survival; and unbound (serum) protein content.通过芥子气在体内诱导产生的兔皮肤损伤在器官培养中释放的炎性介质和调节剂。I. 定量组织病理学;中性粒细胞、嗜碱性粒细胞和单核细胞存活情况;以及未结合(血清)蛋白含量。
Am J Pathol. 1985 Oct;121(1):15-27.
6
Functional anatomy of the lymphatic fluids and pathways.淋巴液和淋巴途径的功能解剖学。
Lymphology. 1975 Jun;8(2):49-56.
7
Partial characterization of a cell-directed inhibitor of leukotaxis in human serum.人血清中一种细胞导向的白细胞趋化抑制剂的部分特性研究
J Lab Clin Med. 1977 Jan;89(1):190-9.
8
Extravascular albumin.血管外白蛋白
N Engl J Med. 1979 Aug 30;301(9):497-8. doi: 10.1056/NEJM197908303010909.
9
Mechanisms of edema formation in myxedema--increased protein extravasation and relatively slow lymphatic drainage.黏液性水肿中水肿形成的机制——蛋白质外渗增加和淋巴引流相对缓慢。
N Engl J Med. 1979 Aug 30;301(9):460-5. doi: 10.1056/NEJM197908303010902.
10
The interstitial-lymphatic flow system.组织间隙-淋巴液流动系统
Int Rev Physiol. 1979;18:215-60.

炎症介质和调节剂在体内由芥子气所致兔皮肤损伤的器官培养中的释放。II. 伊文思蓝染料实验测定血清蛋白在正在形成和愈合损伤中的进入和周转速率。

Inflammatory mediators and modulators release in organ culture from rabbit skin lesions produced in vivo by sulfur mustard. II. Evans blue dye experiments that determined the rates of entry and turnover of serum protein in developing and healing lesions.

作者信息

Harada S, Dannenberg A M, Kajiki A, Higuchi K, Tanaka F, Pula P J

出版信息

Am J Pathol. 1985 Oct;121(1):28-38.

PMID:4050975
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1888044/
Abstract

Extravasated serum seems to be the major modulator of the local inflammatory response, because it provides both proinflammatory and antiinflammatory components. This report describes the rates of entry and turnover of extravasated serum protein in dermal inflammatory lesions produced by the military vesicant sulfur mustard (SM). Rabbits, bearing SM skin lesions, were given an intravenous injection of Evans blue dye, so that at the time of sacrifice, 2 hours later, their skin lesions were 2 hours and 1,2,3,6, and 10 days of age. Evans blue labels serum albumin, a representative serum protein. By multiplying the amount of Evans blue contained in the lesions by a factor that converted micrograms of Evans blue into milligrams of serum protein, the authors could estimate the 2-hour rate of entry of serum protein into these lesions. Serum protein in the lesions was both bound and unbound. The unbound protein was extractable from the lesions into the culture fluids, and, electrophoretically, was similar in composition to serum protein. Grossly edematous peak lesions (1 day of age) contained 7.8 mg of unbound serum protein per square centimeter of skin. Healing lesions (6 and 10 days of age) contained about 4.5 mg/sq cm, and normal skin about 1.7 mg/sq cm. Lesions 1 day of age had the highest rate of serum albumin entry, and about 36% of this Evans-blue-labeled protein was unbound, ie, extractable into the culture fluids. Lesions 3 and 6 days of age had a rate of serum albumin entry that was roughly half that of 1-day lesions, and only about 13% of this entering protein was unbound. Normal skin had a very low rate of serum albumin entry, and only 8% of this entering protein was unbound. The turnover rate of the unbound (extractable) serum protein could be estimated from the 2-hour entry rate of the Evans-blue-labeled albumin and the total protein in the culture fluids. In 1-day lesions, about 25% of the serum protein in the culture fluids was protein which had entered during the last 2 hours, so that 100% of this unbound protein should have been replaced once in 8 hours. In contrast, in 3- and 6-day lesions, this unbound serum protein should have been replaced once in about 35 hours, and in normal skin once in 80 hours. Evans-blue-labeled serum albumin continuously entered both the bound and unbound compartments of the SM lesions, even during the healing stages.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

外渗血清似乎是局部炎症反应的主要调节因子,因为它同时提供促炎和抗炎成分。本报告描述了军事糜烂剂芥子气(SM)所致皮肤炎症病变中外渗血清蛋白的进入速率和更新率。给患有SM皮肤损伤的兔子静脉注射伊文思蓝染料,以便在2小时后处死时,其皮肤损伤分别处于2小时龄以及1、2、3、6和10日龄。伊文思蓝标记血清白蛋白,一种代表性的血清蛋白。通过将损伤部位所含伊文思蓝的量乘以一个将微克伊文思蓝换算为毫克血清蛋白的系数,作者能够估算出血清蛋白进入这些损伤部位的2小时速率。损伤部位的血清蛋白既有结合型的也有未结合型的。未结合蛋白可从损伤部位提取到培养液中,并且在电泳时其组成与血清蛋白相似。严重水肿的高峰损伤(1日龄)每平方厘米皮肤含有7.8毫克未结合血清蛋白。愈合中的损伤(6和10日龄)每平方厘米约含4.5毫克,正常皮肤约含1.7毫克。1日龄的损伤血清白蛋白进入速率最高,且这种伊文思蓝标记的蛋白约36%是未结合的,即可以提取到培养液中。3和6日龄的损伤血清白蛋白进入速率约为1日龄损伤的一半,且这种进入的蛋白只有约13%是未结合的。正常皮肤血清白蛋白进入速率非常低,且这种进入的蛋白只有8%是未结合的。未结合(可提取)血清蛋白的更新率可根据伊文思蓝标记白蛋白的2小时进入速率和培养液中的总蛋白来估算。在1日龄的损伤中,培养液中约25%的血清蛋白是在过去2小时内进入的蛋白,因此这种未结合蛋白应该在8小时内更新一次。相比之下,在3和6日龄的损伤中,这种未结合血清蛋白应该在约35小时内更新一次,而在正常皮肤中则在80小时内更新一次。即使在愈合阶段,伊文思蓝标记的血清白蛋白也持续进入SM损伤的结合和未结合部分。(摘要截选至400字)