Investigation of proton conductance in liver mitochondria of broilers with pulmonary hypertension syndrome
Investigation of proton conductance in liver mitochondria of broilers with pulmonary hypertension syndrome
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DOI：
10.1093/ps/83.2.259
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发表时间：
2004-02-01
期刊：
影响因子：
4.4
通讯作者：
Bottje, WG
中科院分区：
文献类型：
--
作者：
Cawthon, D;Iqbal, M;Bottje, WG
We previously reported an impaired ability to regulate hepatic mitochondrial state 4 respiration rate in response to sequential additions of adenosine diphosphate in pulmonary hypertension syndrome (PHS). As proton conductance is a major contributor to State 4 respiration, the major goal of this study was to investigate the nature of proton conductance in hepatic mitochondria isolated from broilers with and without PHS. Broilers were placed on floor litter in environmental chambers and exposed to cold temperatures (15degreesC) from 3 to 7 wk of age to induce PHS. Liver mitochondria were isolated from birds that exhibited PHS (cyanosis, right ventricular weight ratio > 0.30) or from birds that appeared healthy (no cyanosis, right ventricular weight ratio < 0.27). Isolated mitochondria were placed in a chamber equipped with the ability to measure oxygen content and mitochondrial membrane potential. The mitochondrial membrane potential was assessed by an ion sensitive electrode to measure the distribution of methyltriphenylphosphonium across the inner mitochondrial membrane. Proton conductance was assessed by simultaneously measuring State 4 oxygen consumption rate as respiration was progressively inhibited with increasing concentrations of malonate. The addition of cardiolipin, a lipid found in high concentrations in mitochondrial membranes that can alter proton conductance, had no affect on respiration or mitochondrial membrane potential in either group. The relationship of curves depicting State 4 respiration and mitochondrial membrane potential indicates that PHS mitochondria exhibit impaired substrate oxidation and reduced proton conductance relative to controls. These findings provide further characterization of the altered cellular oxygen utilization in broilers with PHS.
