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Mitochondria Bioenergetic Functions and Cell Metabolism Are Modulated by the Bergamot Polyphenolic Fraction
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作者:

Algieri, Cristina
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Univ Bologna, Dept Vet Med Sci, I-40064 Ozzano Dell Emilia, Italy Univ Bologna, Dept Vet Med Sci, I-40064 Ozzano Dell Emilia, Italy

Bernardini, Chiara
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Univ Bologna, Dept Vet Med Sci, I-40064 Ozzano Dell Emilia, Italy Univ Bologna, Dept Vet Med Sci, I-40064 Ozzano Dell Emilia, Italy

Oppedisano, Francesca
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Magna Graecia Univ Catanzaro, Inst Res Food Safety & Hlth IRC FSH, Dept Hlth Sci, I-88100 Catanzaro, Italy Univ Bologna, Dept Vet Med Sci, I-40064 Ozzano Dell Emilia, Italy

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Palma, Ernesto
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Magna Graecia Univ Catanzaro, Inst Res Food Safety & Hlth IRC FSH, Dept Hlth Sci, I-88100 Catanzaro, Italy Univ Bologna, Dept Vet Med Sci, I-40064 Ozzano Dell Emilia, Italy

Forni, Monica
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Univ Bologna, Dept Vet Med Sci, I-40064 Ozzano Dell Emilia, Italy
Univ Bologna, Alma Mater Studiorum, Interdept Ctr Ind Res CIRI SDV, Hlth Sci & Technol, I-40126 Bologna, Italy Univ Bologna, Dept Vet Med Sci, I-40064 Ozzano Dell Emilia, Italy

Mollace, Vincenzo
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Magna Graecia Univ Catanzaro, Inst Res Food Safety & Hlth IRC FSH, Dept Hlth Sci, I-88100 Catanzaro, Italy Univ Bologna, Dept Vet Med Sci, I-40064 Ozzano Dell Emilia, Italy

Romeo, Giovanni
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St Orsola Malpighi Univ Hosp, Med Genet Unit, Dept Gynecol Obstetr & Pediat Sci, I-40126 Bologna, Italy Univ Bologna, Dept Vet Med Sci, I-40064 Ozzano Dell Emilia, Italy

Nesci, Salvatore
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Univ Bologna, Dept Vet Med Sci, I-40064 Ozzano Dell Emilia, Italy Univ Bologna, Dept Vet Med Sci, I-40064 Ozzano Dell Emilia, Italy
机构:
[1] Univ Bologna, Dept Vet Med Sci, I-40064 Ozzano Dell Emilia, Italy
[2] Magna Graecia Univ Catanzaro, Inst Res Food Safety & Hlth IRC FSH, Dept Hlth Sci, I-88100 Catanzaro, Italy
[3] Univ Bologna, Alma Mater Studiorum, Interdept Ctr Ind Res CIRI SDV, Hlth Sci & Technol, I-40126 Bologna, Italy
[4] St Orsola Malpighi Univ Hosp, Med Genet Unit, Dept Gynecol Obstetr & Pediat Sci, I-40126 Bologna, Italy
来源:
关键词:
mitochondria;
cell metabolism;
F1FO-ATPase;
mitochondrial permeability transition pore;
porcine aortic endothelial cells;
bergamot polyphenolic fraction;
F-ATP SYNTHASE;
PERMEABILITY TRANSITION PORE;
C-SUBUNIT RING;
OXIDATIVE-PHOSPHORYLATION;
F1FO-ATPASE ACTIVITY;
RESPIRATORY ENZYMES;
INHIBITION;
CHANNEL;
OLIGOMYCIN;
CA2+;
D O I:
10.3390/cells11091401
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
The bergamot polyphenolic fraction (BPF) was evaluated in the F1FO-ATPase activity of swine heart mitochondria. In the presence of a concentration higher than 50 mu g/mL BPF, the ATPase activity of F1FO-ATPase, dependent on the natural cofactor Mg2+, increased by 15%, whereas the enzyme activity in the presence of Ca2+ was inhibited by 10%. By considering this opposite BPF effect, the F1FO-ATPase activity involved in providing ATP synthesis in oxidative phosphorylation and triggering mitochondrial permeability transition pore (mPTP) formation has been evaluated. The BPF improved the catalytic coupling of oxidative phosphorylation in the presence of a substrate at the first phosphorylation site, boosting the respiratory control ratios (state 3/state 4) by 25% and 85% with 50 mu g/mL and 100 mu g/mL BPF, respectively. Conversely, the substrate at the second phosphorylation site led to the improvement of the state 3/state 4 ratios by 15% only with 100 mu g/mL BPF. Moreover, the BPF carried out its beneficial effect on the mPTP phenomenon by desensitizing the pore opening. The acute effect of the BPF on the metabolism of porcine aortica endothelial cells (pAECs) showed an ATP rate index greater than one, which points out a prevailing mitochondrial oxidative metabolism with respect to the glycolytic pathway, and this ratio rose by about three times with 100 mu g/mL BPF. Consistently, the mitochondrial ATP turnover, in addition to the basal and maximal respiration, were higher in the presence of the BPF than in the controls, and the MTT test revealed an increase in cell viability with a BPF concentration above 200 mu g/mL. Therefore, the molecule mixture of the BPF aims to ensure good performance of the mitochondrial bioenergetic parameters.
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