19 research outputs found
Sensory evaluation and antioxidant capacity as quality parameters in the development of a banana, strawberry and juçara smoothie
Ursolic acid-mediated changes in glycolytic pathway promote cytotoxic autophagy and apoptosis in phenotypically different breast cancer cells
Anthocyanins: From plant pigments to health benefits at mitochondrial level
Anthocyanins are water-soluble pigments providing certain color for various plant parts, especially in edible berries. Earlier these compounds were only known as natural food colorants, the stability of which depended on pH, light, storage temperature and chemical structure. However, due to the increase of the in vitro, in vivo experimental data, as well as of the epidemiological studies, today anthocyanins and their metabolites are also regarded as potential pharmaceutical compounds providing various beneficial health effects on either human or animal cardiovascular system, brain, liver, pancreas and kidney. Many of these effects are shown to be related to the free-radical scavenging and antioxidant properties of anthocyanins, or to their ability to modulate the intracellular antioxidant systems. However, it is generally overlooked that instead of acting exclusively as antioxidants certain anthocyanins affect the activity of mitochondria that are the main source of energy in cells. Therefore, the aim of the present review is to summarize the major knowledge about the chemistry and regulation of biosynthesis of anthocyanins in plants, to overview the facts on bioavailability, and to discuss the most recent experimental findings related to the beneficial health effects emphasizing mitochondria
Modification of Permeability Transition Pore Arginine(s) by Phenylglyoxal Derivatives in Isolated Mitochondria and Mammalian Cells. Structure-function relationship of arginine ligands
Methylglyoxal and synthetic glyoxal derivatives react
covalently with arginine residue(s) on the mitochondrial
permeability transition pore (PTP). In this study,
we have investigated how the binding of a panel of synthetic
phenylglyoxal derivatives influences the opening
and closing of the PTP. Using both isolated mitochondria
and mammalian cells, we demonstrate that the resulting
arginine-phenylglyoxal adduct can lead to either
suppression or induction of permeability transition, depending
on the net charge and hydrogen bonding capacity
of the adduct. We report that phenylglyoxal derivatives
that possess a net negative charge and/or are
capable of forming hydrogen bonds induced permeability
transition. Derivatives that were overall electroneutral
and cannot form hydrogen bonds suppressed permeability
transition. When mammalian cells were
incubated with low concentrations of negatively
charged phenylglyoxal derivatives, the addition of oligomycin
caused a depolarization of the mitochondrial
membrane potential. This depolarization was completely
blocked by cyclosporin A, a PTP opening inhibitor,
indicating that the depolarization was due to PTP
opening. Collectively, these findings highlight that the
target arginine(s) is functionally linked with the opening/
closing mechanism of the PTP and that the electric
charge and hydrogen bonding of the resulting arginine
adduct influences the conformation of the PTP. These
results are consistent with a model where the target
arginine plays a role as a voltage sensor
Modification of Permeability Transition Pore Arginine(s) by Phenylglyoxal Derivatives in Isolated Mitochondria and Mammalian Cells: Structure-Function Relationship of Arginine Ligands
Methylglyoxal and synthetic glyoxal derivatives react
covalently with arginine residue(s) on the mitochondrial
permeability transition pore (PTP). In this study,
we have investigated how the binding of a panel of synthetic
phenylglyoxal derivatives influences the opening
and closing of the PTP. Using both isolated mitochondria
and mammalian cells, we demonstrate that the resulting
arginine-phenylglyoxal adduct can lead to either
suppression or induction of permeability transition, depending
on the net charge and hydrogen bonding capacity
of the adduct. We report that phenylglyoxal derivatives
that possess a net negative charge and/or are
capable of forming hydrogen bonds induced permeability
transition. Derivatives that were overall electroneutral
and cannot form hydrogen bonds suppressed permeability
transition. When mammalian cells were
incubated with low concentrations of negatively
charged phenylglyoxal derivatives, the addition of oligomycin
caused a depolarization of the mitochondrial
membrane potential. This depolarization was completely
blocked by cyclosporin A, a PTP opening inhibitor,
indicating that the depolarization was due to PTP
opening. Collectively, these findings highlight that the
target arginine(s) is functionally linked with the opening/
closing mechanism of the PTP and that the electric
charge and hydrogen bonding of the resulting arginine
adduct influences the conformation of the PTP. These
results are consistent with a model where the target
arginine plays a role as a voltage sensor