Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
Add more filters

Database
Language
Affiliation country
Publication year range
1.
Food Chem Toxicol ; 154: 112316, 2021 Aug.
Article in English | MEDLINE | ID: mdl-34089800

ABSTRACT

Mitochondria are among the first responders to various stress factors that challenge cell and tissue homeostasis. Various plant alkaloids have been investigated for their capacity to modulate mitochondrial activities. In this study, we used isolated mitochondria from mouse brain and liver tissues to assess nicotine, anatabine and anabasine, three alkaloids found in tobacco plant, for potential modulatory activity on mitochondrial bioenergetics parameters. All alkaloids decreased basal oxygen consumption of mouse brain mitochondria in a dose-dependent manner without any effect on the ADP-stimulated respiration. None of the alkaloids, at 1 nM or 1.25 µM concentrations, influenced the maximal rate of swelling of brain mitochondria. In contrast to brain mitochondria, 1.25 µM anatabine, anabasine and nicotine increased maximal rate of swelling of liver mitochondria suggesting a toxic effect. Only at 1 mM concentration, anatabine slowed down the maximal rate of Ca2+-induced swelling and increased the time needed to reach the maximal rate of swelling. The observed mitochondrial bioenergetic effects are probably mediated through a pathway independent of nicotinic acetylcholine receptors, as quantitative proteomic analysis could not confirm their expression in pure mitochondrial fractions isolated from mouse brain tissue.


Subject(s)
Alkaloids/toxicity , Mitochondria/drug effects , Plants/chemistry , Animals , Brain/drug effects , Brain/metabolism , Energy Metabolism/drug effects , Membrane Potential, Mitochondrial/drug effects , Mice , Mitochondria/metabolism , Proteomics , Receptors, Nicotinic/metabolism
2.
Cell Death Dis ; 10(4): 317, 2019 04 08.
Article in English | MEDLINE | ID: mdl-30962427

ABSTRACT

Melatonin, more commonly known as the sleep hormone, is mainly secreted by the pineal gland in dark conditions and regulates the circadian rhythm of the organism. Its intrinsic properties, including high cell permeability, the ability to easily cross both the blood-brain and placenta barriers, and its role as an endogenous reservoir of free radical scavengers (with indirect extra activities), confer it beneficial uses as an adjuvant in the biomedical field. Melatonin can exert its effects by acting through specific cellular receptors on the plasma membrane, similar to other hormones, or through receptor-independent mechanisms that involve complex molecular cross talk with other players. There is increasing evidence regarding the extraordinary beneficial effects of melatonin, also via exogenous administration. Here, we summarize molecular pathways in which melatonin is considered a master regulator, with attention to cell death and inflammation mechanisms from basic, translational and clinical points of view in the context of newborn care.


Subject(s)
Infant, Newborn, Diseases/drug therapy , Inflammation/drug therapy , Melatonin/physiology , Melatonin/therapeutic use , Autophagy/drug effects , Blood-Brain Barrier/drug effects , Blood-Brain Barrier/metabolism , Cell Death , Female , Free Radical Scavengers/therapeutic use , Humans , Infant, Newborn , Inflammation/metabolism , Melatonin/metabolism , Melatonin/pharmacokinetics , Mitochondrial Membrane Transport Proteins/drug effects , Mitochondrial Membrane Transport Proteins/metabolism , Mitochondrial Permeability Transition Pore , Placenta/drug effects , Placenta/metabolism , Pregnancy , Premature Birth/mortality , Premature Birth/physiopathology , Receptors, Melatonin/metabolism
3.
Curr Med Chem ; 26(19): 3376-3406, 2019.
Article in English | MEDLINE | ID: mdl-28554320

ABSTRACT

Mitochondria are cytoplasmic double-membraned organelles that are involved in a myriad of key cellular regulatory processes. The loss of mitochondrial function is related to the pathogenesis of several human diseases. Over the last decades, an increasing number of studies have shown that dietary polyphenols can regulate mitochondrial redox status, and in some cases, prevent or delay disease progression. This paper aims to review the role of four dietary polyphenols - resveratrol, curcumin, epigallocatechin-3-gallate nd quercetin - in molecular pathways regulated by mitochondria and their potential impact on human health. Cumulative evidence showed that the aforementioned polyphenols improve mitochondrial functions in different in vitro and in vivo experiments. The mechanisms underlying the polyphenols' beneficial effects include, among others, the attenuation of oxidative stress, the regulation of mitochondrial metabolism and biogenesis and the modulation of cell-death signaling cascades, among other mitochondrial-independent effects. The understanding of the chemicalbiological interactions of dietary polyphenols, namely with mitochondria, may have a huge impact on the treatment of mitochondrial dysfunction-related disorders.


Subject(s)
Catechin/analogs & derivatives , Curcumin/therapeutic use , Mitochondria/metabolism , Mitochondrial Diseases/drug therapy , Quercetin/therapeutic use , Resveratrol/therapeutic use , Animals , Catechin/therapeutic use , Humans , Oxidative Stress/drug effects
SELECTION OF CITATIONS
SEARCH DETAIL