Effects of GDP on the activity and expression of mitochondrial uncoupling proteins in rat brain in vitro.
- Author:
Chen XIA
1
;
Jun-Ze LIU
;
Yu XU
Author Information
1. Department of Pathophysiology, College of High Altitude Military Medicine, the Third Military Medical University, Chongqing 400038, China.
- Publication Type:Journal Article
- MeSH:
Animals;
Brain;
drug effects;
metabolism;
Guanosine Diphosphate;
pharmacology;
In Vitro Techniques;
Ion Channels;
metabolism;
Male;
Mitochondria;
drug effects;
metabolism;
Mitochondrial Membrane Transport Proteins;
metabolism;
Mitochondrial Proteins;
metabolism;
Mitochondrial Uncoupling Proteins;
Nerve Tissue Proteins;
metabolism;
RNA, Messenger;
Rats;
Rats, Sprague-Dawley;
Reverse Transcriptase Polymerase Chain Reaction
- From:
Acta Physiologica Sinica
2008;60(4):492-496
- CountryChina
- Language:Chinese
-
Abstract:
To investigate the regulatory role of purine nucleotide on uncoupling proteins (UCPs), the activity of UCPs and the expressions of UCP4 and UCP5 in mitochondria of rat brain tissues incubated with GDP were observed in vitro. The cerebral hemispheres of adult male Sprague-Dawley rats were removed and clipped into 8-10 mm3 tissue mass which incubated with 1 mmol/L GDP (GDP group), or only incubation medium (control group), for 30 min in vitro. The mitochondria from incubated tissue mass of rat brain were isolated by centrifugation. The activity of UCPs was detected by the method of [3H]-GTP binding with UCPs specifically. The maximal binding content (Bmax) and the dissociation constant (Kd) were determined from Scatchard plot. The mRNA and protein expressions of UCP4 and UCP5 were measured by RT-PCR and Western blot, respectively. The results showed that Bmax was increased and Kd was decreased in rat brain mitochondria in GDP group compared with that in control group. But the mRNA and protein expressions of UCP4 and UCP5 exhibited no statistically significant changes. It is thus suggested that GDP inhibits the activity of mitochondrial UCPs in rat brain in vitro, but exhibits no effect on the expressions of UCP4 and UCP5.
