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Featured researches published by Philip Kimbel.


The New England Journal of Medicine | 1981

Elastolytic Activity in Pulmonary Lavage Fluid from Patients with Adult Respiratory-Distress Syndrome

Catherine T. Lee; Alan M. Fein; Michael Lippmann; Henry Holtzman; Philip Kimbel; George Weinbaum

To test the hypothesis that adult respiratory-distress syndrome (ARDS) is related to increased activity of the proteolytic enzyme elastase released from neutrophils in the lung, we determined the differential white-cell count, the elastolytic activity, the source of elastase, and the concentration and activity of the endogenous protease inhibitor alpha-1-antiprotease (alpha-1-AP) in bronchoalveolar lavage fluid from 23 patients with ARDS and from 55 patients without this syndrome. Neutrophil predominance (> 80 per cent) was observed in 18 of 23 patients with ARDS. High elastolytic activity of neutrophil origin was found in 12 of 23 patients with ARDS (52 per cent), in none of 16 normal nonsmokers (P < 0.01), in two of 17 normal smokers, and in three of 22 patients with chronic obstructive pulmonary disease. Although there were no significant differences in alpha-1-AP concentrations, its activity was reduced in eight of nine patients with ARDS and high elastolytic activity. We conclude that in many patients with ARDS, high levels of neutrophil elastolytic activity in the lungs are associated with reduced alpha-1-AP function.


Annals of Internal Medicine | 1964

The Pathophysiology of Scleroderma Involving the Heart and Respiratory System

Marvin A. Sackner; Necati Akgun; Philip Kimbel; David H. Lewis

Excerpt The lungs from patients with scleroderma show varying degrees of pulmonary fibrosis and medial hypertrophy of the pulmonary arterioles (1). However, little attention has been directed towar...


Experimental Lung Research | 1980

The Effect of the Oxidizing Agents Chloramine-T and Cigarette Smoke on Dog Serum Proteinase Inhibitor(s)

William R. Abrams; Abraham Eliraz; Philip Kimbel; George Weinbaum

Dog serum treated with the oxidant chloramine-T is rapidly and selectively depleted of its ability to inhibit porcine pancreatic elastase or dog neutrophil elastase. Trypsin inhibitory capacity of serum is not affected. Purified dog alpha-1-proteinase inhibitor (alpha-1-PI) is similarly oxidized with an apparent rate constant of 1.1 x 10(3) M-1 sec-1. Reversal of the oxidative inactivation using dithiothreitol was demonstrated. Cigarette smoke also directly affects the inhibitory capacity of both serum and pure alpha-1-PI. These studies form a basis for developing a model of functionally deficient alpha-1-PI by taking advantage of oxidative inactivation of normal proteinase inhibitor levels.


Experimental Lung Research | 1988

Acute Cigarette Smoke Exposure in Dogs: The Inflammatory Response

William R. Abrams; Umberto Kucich; Philip Kimbel; Mitchell Glass; George Weinbaum

Acute cigarette smoke causes polymorphonuclear leukocyte (neutrophil, PMN) recruitment to the lung followed by loss of elastase from the recruited cells. Dogs were exposed to cigarette smoke with different oxidant content, bronchoalveolar lavage (BAL) was performed, and the cell distribution in the recovered alveolar lining fluid was analyzed. Exposures were 1, 3, or 6 cigarettes on one or multiple days with a maximum dose of 42 cigarettes. The mean percent PMN present in control lavage was 2.01%, while the mean percent PMN recovered in BAL after a dose of 42 1R1 cigarettes was 13.05%. Recoverable PMN, after a single exposure to three 1R1 cigarettes, also increased from 1.7 to 10.4% by 15 h after cessation of smoke exposure. The cell response for multiple (2 and 7) day exposures was similar. The elastase content per BAL neutrophil decreased relative to peripheral blood PMN from the same animals. No free elastolytic activity was found in BAL, but PMN elastase antigen was present. Increased frequency of cigarette smoke exposure delayed the return to homeostatic cell conditions. The increased PMN accumulation observed may result in an increased proteolytic load in the pulmonary interstitium and contribute to the pathogenesis of emphysema.


Surgery Today | 1973

Hemodynamics in pulmonary embolism, with special reference to pulmonary capillary blood flow

Masao Nagano; Luis E. Nunez; Philip Kimbel

AbstractWe determined the effect of heparin pretreatment in modifying the pulmonary hypertension and reduced pulsatility of pulmonary capillary blood flow (


Annals of the New York Academy of Sciences | 2006

EFFECTS OF INSULIN AND TOLBUTAMIDE ON BLOOD GLUCOSE ENTRY AND REMOVAL RATES

George A. Reichard; A. Gerson Jacobs; Bernice Friedmann; Philip Kimbel; Norman J. Hochella; Sidney Weinhouse


The American review of respiratory disease | 2015

Experimental Emphysema Induced with Purified Human Neutrophil Elastase: Tissue Localization of the Instilled Protease1–4

Aaron Janoff; Bruce Sloan; George Weinbaum; Victor V. Damiano; Robert A. Sandhaus; Jules Elias; Philip Kimbel

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The American review of respiratory disease | 2015

Induction of Experimental Emphysema1,2

Burton Mass; Togo Ikeda; David R. Meranze; George Weinbaum; Philip Kimbel


The American review of respiratory disease | 2015

Immunologic Measurement of Elastin-Derived Peptides in Human Serum1–3

Umberto Kucich; Paul Christner; Michael Lippmann; Alan M. Fein; Alan Goldberg; Philip Kimbel; George Weinbaum; Joel Rosenbloom

) wave observed after thrombo-embolization in dogs. In vivo thrombi were produced in 24 dogs, 12 of which were pretreated with heparin. Pulmonary arterial pressure and


The American review of respiratory disease | 2015

Utilization of a peroxidase antiperoxidase complex in an enzyme-linked immunosorbent assay of elastin-derived peptides in human plasma.

Umberto Kucich; Paul Christner; Michael Lippmann; Philip Kimbel; Greg Williams; Joel Rosenbloom; George Weinbaum

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George Weinbaum

Albert Einstein Medical Center

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William R. Abrams

University of Pennsylvania

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Umberto Kucich

University of Pennsylvania

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Bruce Sloan

Albert Einstein Medical Center

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Joel Rosenbloom

Thomas Jefferson University

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A. Gerson Jacobs

Albert Einstein Medical Center

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Michael Lippmann

Albert Einstein Medical Center

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