Literature DB >> 4050975

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.

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

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)

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Year:  1985        PMID: 4050975      PMCID: PMC1888044     

Source DB:  PubMed          Journal:  Am J Pathol        ISSN: 0002-9440            Impact factor:   4.307


  11 in total

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Authors:  S Rodbard; P Feldman
Journal:  Lymphology       Date:  1975-06       Impact factor: 1.286

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Review 3.  The interstitial-lymphatic flow system.

Authors:  B W Zweifach; A Silberberg
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Authors:  M A Rothschild; M Oratz; S S Schreiber
Journal:  N Engl J Med       Date:  1979-08-30       Impact factor: 91.245

Review 5.  Formation of human plasma kinin.

Authors:  R W Colman
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Review 6.  Endogenous anti-inflammatory factors.

Authors:  D A Lewis
Journal:  Biochem Pharmacol       Date:  1984-06-01       Impact factor: 5.858

Review 7.  Protein inhibitors of proteinases.

Authors:  M Laskowski; I Kato
Journal:  Annu Rev Biochem       Date:  1980       Impact factor: 23.643

8.  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.

Authors:  A M Dannenberg; P J Pula; L H Liu; S Harada; F Tanaka; R F Vogt; A Kajiki; K Higuchi
Journal:  Am J Pathol       Date:  1985-10       Impact factor: 4.307

9.  Pathogenesis of skin lesions caused by sulfur mustard.

Authors:  R F Vogt; A M Dannenberg; B H Schofield; N A Hynes; B Papirmeister
Journal:  Fundam Appl Toxicol       Date:  1984-04

10.  Mechanisms of edema formation in myxedema--increased protein extravasation and relatively slow lymphatic drainage.

Authors:  H H Parving; J M Hansen; S L Nielsen; N Rossing; O Munck; N A Lassen
Journal:  N Engl J Med       Date:  1979-08-30       Impact factor: 91.245

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  7 in total

1.  Chemotactic factors released in culture by intact developing and healing skin lesions produced in rabbits by the irritant sulfur mustard.

Authors:  F Tanaka; A M Dannenberg; K Higuchi; M Nakamura; P J Pula; T E Hugli; R G Discipio; D L Kreutzer
Journal:  Inflammation       Date:  1997-04       Impact factor: 4.092

2.  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.

Authors:  K Higuchi; A Kajiki; M Nakamura; S Harada; P J Pula; A L Scott; A M Dannenberg
Journal:  Inflammation       Date:  1988-08       Impact factor: 4.092

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4.  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.

Authors:  A M Dannenberg; P J Pula; L H Liu; S Harada; F Tanaka; R F Vogt; A Kajiki; K Higuchi
Journal:  Am J Pathol       Date:  1985-10       Impact factor: 4.307

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.

Authors:  J Tsuruta; K Sugisaki; A M Dannenberg; T Yoshimura; Y Abe; P Mounts
Journal:  Inflammation       Date:  1996-06       Impact factor: 4.092

6.  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.

Authors:  S Harada; A M Dannenberg; R F Vogt; J E Myrick; F Tanaka; L C Redding; R M Merkhofer; P J Pula; A L Scott
Journal:  Am J Pathol       Date:  1987-01       Impact factor: 4.307

7.  Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.

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Journal:  BMC Genomics       Date:  2021-06-09       Impact factor: 4.547

  7 in total

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