Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 5 de 5
Filter
Add more filters











Publication year range
1.
J Am Nutr Assoc ; 42(8): 783-789, 2023.
Article in English | MEDLINE | ID: mdl-37871299

ABSTRACT

OBJECTIVE: The aim of this study is to evaluate the effect of avocado oil on the histoarchitecture of the prostate of normal rats and on rats with induced benign prostatic hyperplasia using computerized histomorphometry and immunohistochemistry. METHODS: Twenty-eight Wistar rats were divided into four groups: the control group (CG), the avocado oil group (AOG) fed with avocado oil-based diet, the induced group (IG), and the avocado oil testosterone-induced group (AOIG). Prostate hyperplasia was induced by subcutaneous implantation of silicone pellets, filled with testosterone, to promote androgen stimulation. After 12 weeks, the rats were euthanized, and their prostates were removed. The material was prepared for paraffin processing and stained using hematoxylin-eosin and immunostaining for p63 nuclear antigen. RESULTS: The mean epithelial thickness obtained from AOIG (19.44 ± 2.62 µm) was significantly reduced compared to that from IG (27.02 ± 4.1 µm). The average alveolar area in AOIG was 0.100 ± 0.03, which was greater than that of CG. The immunostaining for p63 in basal cells in AOIG was 17.77% ± 2.72 of the total area, a result greater than that in AOG (12.13% ± 2.04) and CG (12.01 ± 2.05). Collagen remodeling was observed with thicker fibers predominating in CG and AOG over thinner fibers in IG and AOIG. CONCLUSION: The results suggest that avocado oil has a protective effect on the prostatic epithelium of Wistar rats subjected to long-term induced prostate hyperplasia.


Subject(s)
Persea , Prostatic Hyperplasia , Male , Humans , Rats , Animals , Prostatic Hyperplasia/drug therapy , Rats, Wistar , Hyperplasia , Testosterone/adverse effects , Cell Proliferation
2.
Food Res Int ; 111: 168-177, 2018 09.
Article in English | MEDLINE | ID: mdl-30007673

ABSTRACT

In this study the effect of lecithin (L) addition and solvent quality in a well-established oleogel system formed by ß-sitosterol and γ-oryzanol (BG) was investigated. Medium chain triglycerides (MCT) and sunflower oil (SFO) were used as triglycerides and hexadecane (HEX) as a model of linear hydrocarbon. Lecithin was proposed due to its natural and versatile properties, showing different functionalities such as emulsifier and co-oleogelator. A study based on hierarchical organization of structured oil was performed applying techniques for bulk, meso and nanoscale. Self-sustained structures could no longer be observed after 40 wt% of BG replacement by lecithin. Small-angle X-ray scattering showed that the formed nanostructures (building blocks) were dependent on type of solvent and BG:L ratio in the mixture of oleogelators. Differential scanning calorimetry showed that stability against temperature was improved decreasing the polarity of the oil, and a time-dependent self-assembly of hybrid systems was observed from thermal and rheological measurements. Microscopy images exhibited changes on typical fibril aggregation of BG as lecithin was added, which promoted to a certain extent the suppression of ribbons. Oscillatory shear and uniaxial compression measurements were influenced by BG:L ratio and solvent mainly at higher lecithin amount. The combination of BG and MCT appeared to be the most affected by lecithin incorporation whereas SFO rendered harder oleogels. These results could contribute to understand the role of both lecithin and solvent type influencing the host oleogelator structure. It was hypothesized that intermolecular BG complex formation is hindered by lecithin, besides this phospholipid also might coexist as a different phase, causing structural changes in the gel network. Addressing the role of co-oleogelator it can provide the opportunity to tune soft materials with adjusted properties.


Subject(s)
Lecithins/analysis , Lecithins/chemistry , Phytosterols/analysis , Phytosterols/chemistry , Calorimetry, Differential Scanning , Crystallization , Organic Chemicals/analysis , Organic Chemicals/chemistry , Phenylpropionates/chemistry , Sitosterols/chemistry , Sunflower Oil/chemical synthesis , Triglycerides/chemistry
3.
Food Chem ; 240: 441-447, 2018 Feb 01.
Article in English | MEDLINE | ID: mdl-28946296

ABSTRACT

The aims of this study were the optimization and validation of a new ultrasound assisted phytosterol method through analysis of response surface generated from Box-Behnken design. Variables quantity of sample (g), volume of KOH/MeOH (mL) and ultrasound time (s) were investigated in three levels. The evaluation process of the methodology was executed through determination of analytical parameters, such as selectivity, linearity, accuracy, dynamic linear range, "intra-day" accuracy and limits of detection and quantification. Optimized conditions for stigmasterol determination were 0.25g; 2.5mL; 300s; and ß-sitosterol were 0.25g; 5.4mL; 300s. The evaluated conditions and all investigated analytical parameters showed that the method is effective for determination of analytes ß-sitosterol and stigmasterol. This new analytical method has the same efficiency of the traditional method, while significantly reducing the total time of extraction for 300s regarding saponification step when compared to 3600s from the traditional method.


Subject(s)
Phytosterols/analysis , Plant Oils/chemistry , Sitosterols , Stigmasterol , Ultrasonic Waves
4.
Arq. ciências saúde UNIPAR ; 14(1)jan-abr. 2010. tab
Article in Portuguese | LILACS | ID: lil-601329

ABSTRACT

A espécie Bromelia antiacantha Bertol. (Bromeliaceae), conhecida como caraguatá ou gravatá, foi avaliada quanto à sua propriedade hemolítica frente a hemácias de sangue de carneiro. O extrato aquoso dos frutos apresentou atividade hemolítica a partir da diluição de 0,85%, enquanto que o extrato aquoso das folhas apresentou hemólise a partir da diluição de 0,90%. Tal atividade pode estar relacionada à presença de saponinas, uma vez que o estudo químico do extrato metanólico das folhas resultou no isolamento da saponina daucosterol, um fitoesterol glicosilado


The specie Bromelia antiacantha Bertol. (Bromeliaceae), popularly known as caraguatá or gravatá, was evaluated as for its hemolytic property against sheep red blood cells. The aqueous extract of the fruits presented hemolytic activity starting from the dilution of 0,85%, while the aqueous extract of the leaves presented hemolysis starting from the dilution of 0,90%. The activity should be related to the presence of saponins, once the chemical study of the leaves methanolic extract resulted in the isolation of the saponin daucosterol, a glycosylated phytosterol.


Subject(s)
Bromeliaceae , Eryngium
5.
Rev. bras. farmacogn ; 18(1): 47-52, jan.-mar. 2008. ilus, tab
Article in English | LILACS | ID: lil-480837

ABSTRACT

Amongst the different forms of therapy to prevent and cure illnesses, plants have been, undoubtedly, the most utilized ones since the beginning of mankind. Brazil has a great diversity on plants that possess non-researched medicinal potential and are promising sources of therapeutic and pharmacological innovations. The Rubiaceae family is considered the biggest one of the order Gentianales, presenting around 637 genera and 10,700 species. Richardia grandiflora (Cham. & Schltdl.) Steud., known popularly as "ervanço", "poaia" or "ipeca-mirim", has ethnopharmacological indications to use as decoction against hemorrhoids and as vermifuge. Aiming at contributing to the chemotaxonomic study of the family Rubiaceae and considering the absence of data in literature about the chemical constitution of the species Richardia grandiflora, the latter was submitted to a phytochemical study to isolate its chemical constituents, through usual chromatographic methods, and after identifying them by means of spectroscopic methods such as ÕH and 13C NMR, with the add of two-dimensional techniques, besides comparison with literature data. Five constituents were isolated through this first phytochemical study with R. grandiflora: a mixture of the steroids beta-sitosterol and stigmasterol, o-hydroxy-benzoic acid, m-methoxy-p-hydroxy-benzoic acid and phaeophitin A, all of them isolated for the first time from the genus Richardia.


Dentre as diversas formas de terapia para a prevenção e cura de doenças, as plantas foram, indubitavelmente, as mais amplamente utilizadas desde o início da humanidade. O Brasil tem grande diversidade de plantas com potenciais medicinais, ainda não pesquisados, e que são promissoras fontes de inovações terapêuticas e farmacológicas. A família Rubiaceae, considerada a maior da ordem Gentianales, possui cerca de 637 gêneros e 10.700 espécies. Richardia grandiflora (Cham. & Schltdl.) Steud., conhecida popularmente como ervanço, poaia ou ipeca-mirim, tem indicações etnofarmacológicas para uso contra hemorróidas e como vermífugo na forma de decocto. Visando a contribuir com o estudo quimiotaxonômico da família Rubiaceae e tendo em vista a ausência de dados na literatura acerca da constituição química de Richardia grandiflora, esta foi submetida a um estudo fitoquímico para o isolamento de seus constituintes químicos, através dos métodos cromatográficos usuais, e posterior identificação estrutural dos mesmos, utilizando-se os métodos espectroscópicos de RMN ÕH e 13C uni e bidimensionais, além de comparações com modelos da literatura. Deste estudo pioneiro com R. grandiflora foram isolados e identificados cinco constituintes: uma mistura dos esteróides beta-sitosterol e estigmasterol, o ácido o-hidroxibenzóico, o ácido m-metoxi-p-hidroxi-benzóico e a feofitina A, todos inéditos no gênero Richardia.


Subject(s)
Stigmasterol/isolation & purification , Stigmasterol/chemistry , Pheophytins/isolation & purification , Pheophytins/chemistry , Hydroxybenzoates , Rubiaceae/chemistry
SELECTION OF CITATIONS
SEARCH DETAIL