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1.
Biopreserv Biobank ; 18(5): 403-408, 2020 Oct.
Article in English | MEDLINE | ID: mdl-32799560

ABSTRACT

l-Carnitine (LC) plays a key role in sperm metabolism, easily providing energy through ß-oxidation, which positively affects motility. The objective of this study was to investigate the association between blood plasma and seminal plasma LC levels, as well as the effect of LC as an additive in a skimmed milk-based extender during sperm storage at 5°C. In the first experiment, semen and blood samples from 14 Quarter Horse stallions were used. The LC content in blood plasma and seminal plasma was determined by spectrophotometry and their relationships with seminal parameters were evaluated. In the second experiment, ejaculates (n = 16) from four Quarter Horses were used. Each ejaculate was split into four treatment groups with different LC concentrations: 0 (control), 0.5, 1.0, and 2.0 mM. Sperm motility, integrity of plasma and acrosomal membranes, intracellular reactive oxygen species content, and plasma membrane stability were evaluated immediately after samples reached 5°C (0 hour) and after 24, 48, and 72 hours. There was a positive correlation (p < 0.05) between LC levels in seminal plasma with both sperm concentration and plasma and acrosomal membrane integrity. Furthermore, the addition of LC (1 and 2 mM) preserved the motility of equine sperm stored at 5°C. It was concluded that the concentrations of LC with seminal plasma present correlate to semen parameters and the addition of LC to skimmed milk-based extender preserves the motility of equine sperm stored at 5°C for up to 48 hours.


Subject(s)
Semen Preservation , Sperm Motility , Animals , Carnitine , Horses , Humans , Male , Semen , Semen Analysis , Spermatozoa
2.
Analyst ; 144(17): 5232-5244, 2019 Sep 07.
Article in English | MEDLINE | ID: mdl-31360935

ABSTRACT

Leishmaniasis comprises a group of infectious diseases with worldwide distribution, of which both the visceral and cutaneous forms are caused by Leishmania parasites. In the absence of vaccines, efficacious chemotherapy remains the basis for leishmaniasis control. The available drugs are expensive and associated with several secondary adverse effects. Due to these limitations, the development of new antileishmanial compounds is imperative, and plants offer various perspectives in this regard. The present study evaluated the in vitro leishmanicidal activity of flavonoids isolated from Solanum paludosum Moric. and investigated the mechanisms of cell death induced by them. These compounds were evaluated in vitro for their antileishmanial activity against Leishmania amazonensis promastigotes and they showed prominent leishmanicidal activity. The EtOAc fraction, gossypetin 3,7,8,4'-tetra-O-methyl ether (1), and kaempferol 3,7-di-O-methyl ether (3) were selected to be used in an in vitro assay against L. amazonensis amastigotes and cell death assays. The flavonoids (1) and (3) presented significant activity against L. amazonensis amastigotes, exhibiting the IC50 values of 23.3 ± 4.5 µM, 34.0 ± 9.6 µM, and 10.5 ± 2.5 µM for the EtOAc fraction, (1), and (3), respectively, without toxic effects to the host cells. Moreover, (1) and (3) induced blocked cell cycle progression at the G1/S transition, ultimately leading to G1/G0 arrest. Flavonoid (3) also induced autophagy. Using Raman spectroscopy in conjunction with principal component analysis, the biochemical changes in the cellular components induced by flavonoids (1) and (3) were presented. The obtained results indicated that the mechanisms of action of (1) and (3) occurred through different routes. The results support that the flavonoids derived from S. paludosum can become lead molecules for the design of antileishmanial prototypes.


Subject(s)
Antiprotozoal Agents/pharmacology , Cell Death/drug effects , Flavonoids/pharmacology , Flow Cytometry/methods , Leishmania/drug effects , Animals , Antiprotozoal Agents/chemistry , Autophagy/drug effects , Cell Line , Cell Survival/drug effects , Drug Evaluation, Preclinical , Flavonoids/chemistry , Kaempferols/chemistry , Kaempferols/pharmacology , Leishmania/cytology , Macrophages/cytology , Macrophages/drug effects , Mice , Spectrum Analysis, Raman , Streptophyta/chemistry
3.
Molecules ; 21(1): E11, 2015 Dec 22.
Article in English | MEDLINE | ID: mdl-26703549

ABSTRACT

The Cactaceae family is composed by 124 genera and about 1438 species. Pilosocereus gounellei, popularly known in Brazil as xique-xique, is used in folk medicine to treat prostate inflammation, gastrointestinal and urinary diseases. The pioneering phytochemical study of P. gounellei was performed using column chromatography and HPLC, resulting in the isolation of 10 substances: pinostrobin (1), ß-sitosterol (2), a mixture of sitosterol 3-O-ß-d-glucopyranoside/stigmasterol 3-O-ß-d-glucopyranoside (3a/3b), 13²-hydroxyphaeophytin a (4), phaeophytin a (5), a mixture of ß-sitosterol and stigmasterol (6a/6b), kaempferol (7), quercetin (8), 7'-ethoxy-trans-feruloyltyramine (mariannein, 9) and trans-feruloyl tyramine (10). Compound 9 is reported for the first time in the literature. The structural characterization of the compounds was performed by analyses of 1-D and 2-D NMR data. In addition, a phenolic and flavonol total content assay was carried out, and the anti-oxidant potential of P. gounellei was demonstrated.


Subject(s)
Antioxidants/chemistry , Cactaceae/chemistry , Plant Extracts/chemistry , Plant Extracts/pharmacology , Antioxidants/pharmacology , Chromatography, High Pressure Liquid , Coumaric Acids/chemistry , Coumaric Acids/pharmacology , Flavonoids/chemistry , Flavonoids/pharmacology , Medicine, Traditional , Molecular Structure , Phenols/chemistry , Phenols/pharmacology , Tyramine/analogs & derivatives , Tyramine/chemistry , Tyramine/pharmacology
4.
Molecules ; 19(4): 5434-47, 2014 Apr 24.
Article in English | MEDLINE | ID: mdl-24879587

ABSTRACT

This paper presents the quantification, antioxidant and antimicrobial activity of capsaicin, dihydrocapsaicin and the flavonoid chrysoeriol isolated from different extracts (hexane and acetonitrile extracts from whole fruit, peel and seed) of Capsicum frutescens (pimenta malagueta). The acetonitrile extract of the seeds, peel and whole fruits contained capsaicin as a major component, followed in abundance by dihydrocapsaicin and chrysoeriol. The antimicrobial activity of the isolated compounds against seven microorganisms showed chrysoeriol was the most active compound. In the antioxidant test, the acetonitrile extract from the whole fruit showed the highest activity. The antioxidant activity of pimenta malagueta may be correlated with its phenolic content, principally with the most active compound, capsaicin.


Subject(s)
Anti-Bacterial Agents/chemistry , Capsicum/chemistry , Free Radical Scavengers/chemistry , Phenols/chemistry , Plant Extracts/chemistry , Anti-Bacterial Agents/pharmacology , Antifungal Agents/chemistry , Antifungal Agents/pharmacology , Benzothiazoles/chemistry , Biphenyl Compounds/chemistry , Candida albicans/drug effects , Free Radical Scavengers/pharmacology , Free Radicals/chemistry , Fruit/chemistry , Gram-Negative Bacteria/drug effects , Gram-Positive Bacteria/drug effects , Microbial Sensitivity Tests , Phenols/pharmacology , Picrates/chemistry , Plant Extracts/pharmacology , Sulfonic Acids/chemistry
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