Journal of Applied Physiology AJP: Heart and Circulatory Physiology
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J Appl Physiol (March 22, 2002). doi:10.1152/japplphysiol.00635.2000
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Articles in PresS, published online ahead of print March 22, 2002
J Appl Physiol, 10.1152/jap.00635.2000
Submitted on July 5, 2000
Accepted on March 19, 2002

NEUTRAL AND DEAE DEXTRANS AS TRACERS FOR ASSESSING PULMONARY MICROVASCULAR BARRIER PERMEABILITY AND INTEGRITY

Jonathan R Sanders1, N. Adrienne Pou2, and Robert J Roselli3*

1 Department of Biomedical Engineering, Vanderbilt University, Nashville, TN, USA
2 Center for Lung Research, Vanderbilt University, Nashville, TN, USA
3 Department of Biomedical Engineering, Vanderbilt University, Nashville, TN, USA; Center for Lung Research, Vanderbilt University, Nashville, TN, USA

* To whom correspondence should be addressed. E-mail: jrs{at}vuse.vanderbilt.edu.

The steady-state lymph to plasma concentration ratios (L/Ps) of neutral dextrans, cationic DEAE dextrans, and endogenous proteins were determined under normal and increased permeability conditions in six unanesthetized yearling sheep prepared with chronic lung lymph fistulas. Fluorescent dextrans with radii ranging from 1-30 nm were intravenously infused, and after 24 hours, Perilla ketone (PK) was given to alter permeability while maintaining the dextran infusion. Plasma and lymph samples were collected before and after PK administration and analyzed for dextran and protein concentrations following HPLC size separation. Under both baseline and increased permeability conditions, DEAE dextrans had higher L/Ps than neutral dextrans of similar size, but lower L/Ps than proteins of similar size. Comparison of L/Ps before and after PK revealed that the percentage change in permeability for neutral and DEAE dextrans was significantly larger than for proteins. These results suggest that 1) the pulmonary microvascular barrier behaves as a net negative barrier, 2) some transport mechanisms for proteins and dextrans are different, and 3) neutral and cationic dextrans are more sensitive markers than proteins of the same size for assessing changes in pulmonary capillary permeability.




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