Mitochondrial Oxygen Consumption by the Foreskin and its Fibroblast-rich Culture

Objectives: This study investigated the feasibility of using a phosphorescence oxygen analyser to measure cellular respiration (mitochondrial O2 consumption) in foreskin samples and their fibroblast-rich cultures.Methods: Foreskin specimens from normal infants were collected immediately after circum...

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Main Authors: Fatma Al-Jasmi, Thachillath Pramathan, Adnan Swid, Bahjat Sahari, Harvey S. Penefsky, Abdul-Kader Souid
Format: Article
Language:English
Published: Sultan Qaboos University 2013-08-01
Series:Sultan Qaboos University Medical Journal
Subjects:
Online Access:https://journals.squ.edu.om/index.php/squmj/article/view/1840
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author Fatma Al-Jasmi
Thachillath Pramathan
Adnan Swid
Bahjat Sahari
Harvey S. Penefsky
Abdul-Kader Souid
author_facet Fatma Al-Jasmi
Thachillath Pramathan
Adnan Swid
Bahjat Sahari
Harvey S. Penefsky
Abdul-Kader Souid
author_sort Fatma Al-Jasmi
collection DOAJ
description Objectives: This study investigated the feasibility of using a phosphorescence oxygen analyser to measure cellular respiration (mitochondrial O2 consumption) in foreskin samples and their fibroblast-rich cultures.Methods: Foreskin specimens from normal infants were collected immediately after circumcision and processed for measuring cellular respiration and for culture. Cellular mitochondrial O2 consumption was determined as a function of time from the phosphorescence decay of the Pd (II) meso-tetra-(4-sulfonatophenyl)-tetrabenzoporphyrin. Results: In sealed vials containing a foreskin specimen and glucose, O2 concentration decreased linearly with time, confirming the zero-order kinetics of O2 consumption by cytochrome oxidase. Cyanide inhibited O2 consumption, confirming that the oxidation occurred mainly in the mitochondrial respiratory chain. The rate of foreskin respiration (mean ± SD) was 0.074 ± 0.02 μM O2 min-1 mg-1 (n = 23). The corresponding rate for fibroblast-rich cultures was 9.84 ± 2.43 μM O2 min-1 per 107 cells (n = 15). Fibroblast respiration was significantly lower in a male infant with dihydrolipoamide dehydrogenase gene mutations, but normalised with the addition of thiamine or carnitine. Conclusion: The foreskin and its fibroblast-rich culture are suitable for assessment of cellular respiration. However, the clinical utility of foreskin specimens to detect disorders of impaired cellular bioenergetics requires further investigation.
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spelling doaj.art-796c28694c82469d986b2ccd7abdd0e32022-12-22T01:38:23ZengSultan Qaboos UniversitySultan Qaboos University Medical Journal2075-051X2075-05282013-08-011334114161764Mitochondrial Oxygen Consumption by the Foreskin and its Fibroblast-rich CultureFatma Al-Jasmi0Thachillath Pramathan1Adnan Swid2Bahjat Sahari3Harvey S. Penefsky4Abdul-Kader Souid5Department of Paediatrics, College of Medicine & Health Sciences, United Arab Emirates University, Al Ain, United Arab EmiratesDepartment of Paediatrics, College of Medicine & Health Sciences, United Arab Emirates University, Al Ain, United Arab EmiratesTawam Hospital, Al Ain, United Arab EmiratesTawam Hospital, Al Ain, United Arab EmiratesFaculty of Medicine & Health Sciences, United Arab Emirates University, Al Ain, United Arab EmiratesDepartment of Paediatrics, College of Medicine & Health Sciences, United Arab Emirates University, Al Ain, United Arab EmiratesObjectives: This study investigated the feasibility of using a phosphorescence oxygen analyser to measure cellular respiration (mitochondrial O2 consumption) in foreskin samples and their fibroblast-rich cultures.Methods: Foreskin specimens from normal infants were collected immediately after circumcision and processed for measuring cellular respiration and for culture. Cellular mitochondrial O2 consumption was determined as a function of time from the phosphorescence decay of the Pd (II) meso-tetra-(4-sulfonatophenyl)-tetrabenzoporphyrin. Results: In sealed vials containing a foreskin specimen and glucose, O2 concentration decreased linearly with time, confirming the zero-order kinetics of O2 consumption by cytochrome oxidase. Cyanide inhibited O2 consumption, confirming that the oxidation occurred mainly in the mitochondrial respiratory chain. The rate of foreskin respiration (mean ± SD) was 0.074 ± 0.02 μM O2 min-1 mg-1 (n = 23). The corresponding rate for fibroblast-rich cultures was 9.84 ± 2.43 μM O2 min-1 per 107 cells (n = 15). Fibroblast respiration was significantly lower in a male infant with dihydrolipoamide dehydrogenase gene mutations, but normalised with the addition of thiamine or carnitine. Conclusion: The foreskin and its fibroblast-rich culture are suitable for assessment of cellular respiration. However, the clinical utility of foreskin specimens to detect disorders of impaired cellular bioenergetics requires further investigation.https://journals.squ.edu.om/index.php/squmj/article/view/1840oxygenmitochondriaforeskinrespirationfibroblastsdihydrolipoamide dehydrogenasethiaminecarnitine
spellingShingle Fatma Al-Jasmi
Thachillath Pramathan
Adnan Swid
Bahjat Sahari
Harvey S. Penefsky
Abdul-Kader Souid
Mitochondrial Oxygen Consumption by the Foreskin and its Fibroblast-rich Culture
Sultan Qaboos University Medical Journal
oxygen
mitochondria
foreskin
respiration
fibroblasts
dihydrolipoamide dehydrogenase
thiamine
carnitine
title Mitochondrial Oxygen Consumption by the Foreskin and its Fibroblast-rich Culture
title_full Mitochondrial Oxygen Consumption by the Foreskin and its Fibroblast-rich Culture
title_fullStr Mitochondrial Oxygen Consumption by the Foreskin and its Fibroblast-rich Culture
title_full_unstemmed Mitochondrial Oxygen Consumption by the Foreskin and its Fibroblast-rich Culture
title_short Mitochondrial Oxygen Consumption by the Foreskin and its Fibroblast-rich Culture
title_sort mitochondrial oxygen consumption by the foreskin and its fibroblast rich culture
topic oxygen
mitochondria
foreskin
respiration
fibroblasts
dihydrolipoamide dehydrogenase
thiamine
carnitine
url https://journals.squ.edu.om/index.php/squmj/article/view/1840
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