The lungs are a site for the uptake, accumulation, and storage of exogenous basic amines. The compound N-N-N'-trimethyl-N'-(2-hydroxy-3-methyl-5-iodobenzyl)-1,3 propanediamine (HIPDM) is a basic amine that can be labelled with radioactive iodine and detected by external counting, Intravenously injected I-123-HIPDM is extracted by the human lung, where it is retained in a slowly effuxable pool. In the present study, we measured HIPDM lung kinetics and subcellular distribution in rabbits given i.v. I-125-HIPDM. Rabbits were killed from 2 min to 5 h after injection, and the radioactivity retained in their lungs was measured, Subcellular lung fractions (nuclear, mitochondrial, lysosomal, microsomal, and postmicrosomal supernatant) were assayed for HIPDM radioactivity, protein contene, and distribution of specific marker enzymes. HIPDM lung clearance in rabbits was nearly identical to that of humans, Virtually all the HIPDM radioactivity in lungs (98+1%) was associated with subcellular membranous structures. The highest HIPDM specific radioactivity was found in the mitochondrial Fraction, and the subcellular distribution profile closely resembled that of the mitochondrial marker enzyme succinate cytochrome c reductase, No redistribution of HIPDM among subcellular compartments was observed over a 5 h period after injection. The data indicate that mitochondria act as reservoir for HIPDM in the lungs and contribute to the pulmonary persistence of this compound, HIPDM can be used to investigate the pulmonary uptake of basic amines in health and in lung disease.

Mitochondria act as a reservoir for the basic amine HIPDM in the lung

M Miniati;S Monti;
1996

Abstract

The lungs are a site for the uptake, accumulation, and storage of exogenous basic amines. The compound N-N-N'-trimethyl-N'-(2-hydroxy-3-methyl-5-iodobenzyl)-1,3 propanediamine (HIPDM) is a basic amine that can be labelled with radioactive iodine and detected by external counting, Intravenously injected I-123-HIPDM is extracted by the human lung, where it is retained in a slowly effuxable pool. In the present study, we measured HIPDM lung kinetics and subcellular distribution in rabbits given i.v. I-125-HIPDM. Rabbits were killed from 2 min to 5 h after injection, and the radioactivity retained in their lungs was measured, Subcellular lung fractions (nuclear, mitochondrial, lysosomal, microsomal, and postmicrosomal supernatant) were assayed for HIPDM radioactivity, protein contene, and distribution of specific marker enzymes. HIPDM lung clearance in rabbits was nearly identical to that of humans, Virtually all the HIPDM radioactivity in lungs (98+1%) was associated with subcellular membranous structures. The highest HIPDM specific radioactivity was found in the mitochondrial Fraction, and the subcellular distribution profile closely resembled that of the mitochondrial marker enzyme succinate cytochrome c reductase, No redistribution of HIPDM among subcellular compartments was observed over a 5 h period after injection. The data indicate that mitochondria act as reservoir for HIPDM in the lungs and contribute to the pulmonary persistence of this compound, HIPDM can be used to investigate the pulmonary uptake of basic amines in health and in lung disease.
1996
Istituto di Fisiologia Clinica - IFC
basic amines
HIPDM
lung
mitochondria
File in questo prodotto:
File Dimensione Formato  
prod_210941-doc_48122.pdf

solo utenti autorizzati

Descrizione: ERJ 1996
Dimensione 198.01 kB
Formato Adobe PDF
198.01 kB Adobe PDF   Visualizza/Apri   Richiedi una copia

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/177289
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus ND
  • ???jsp.display-item.citation.isi??? 15
social impact