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1.
Toxins (Basel) ; 15(1)2023 01 03.
Artículo en Inglés | MEDLINE | ID: mdl-36668856

RESUMEN

Fridericia chica (Bignoniaceae) is a Colombian Caribbean plant with numerous health benefits, including properties such as wound healing, immune system stimulation, and antioxidant capacity, among others. Mycotoxins alpha-zearalenol (α-ZEL) and beta-zearalenol (ß-ZEL) are phase I metabolites of zearalenone, a natural product involved in endocrine disruption and cell proliferation processes. This study aimed to investigate the cytotoxic potential of the hydroethanolic extract of F. chica leaves (HEFc) and determine their protective effects against proliferation induced by α-ZEL and ß-ZEL on human hepatoma HepG2, lung cancer Calu-1, and primary normal human epidermal keratinocytes, neonatal (HEKn). The cytotoxicity of HEFc was measured in a range from 4 to 1000 µg/mL and from 0.4 to 100 µM for both α-ZEL and ß-ZEL. Cell production of intracellular ROS was monitored using the H2-DCFDA probe. The cells exposed to HEFc presented IC50 of 128, 249, and 602 µg/mL for the HepG2, Calu-1, and HEKn cells, respectively. A greater selectivity was seen in HepG2 cells [selectivity index (SI) = 3.5] than in Calu-1 cells (SI = 2.4). Cells treated with mycotoxins remained viable during the first day, and cell proliferation increased at low tested concentrations (0.4-6.3 µM) in all three cell lines. However, after 48 h treatment, cells exposed to 50 and 100 µM of α-ZEL and ß-ZEL displayed decreased viability. HEFc at 16 µg/mL was able to give some protection against cytotoxicity induced by high concentrations of ß-ZEL in HepG2, reducing also cell proliferation elicited at low levels of α-ZEL and ß-ZEL. ROS production was not observed in cells treated with this HEFc concentration; however, it prevented ROS formation induced by treatment with 50 µM α-ZEL or ß-ZEL. In summary, HEFc isolated from plants grown in northern Colombia displayed promising results against cell proliferation and oxidative stress caused by mycotoxins.


Asunto(s)
Bignoniaceae , Neoplasias Pulmonares , Micotoxinas , Zearalenona , Recién Nacido , Humanos , Antioxidantes/farmacología , Especies Reactivas de Oxígeno , Zearalenona/toxicidad , Micotoxinas/toxicidad , Línea Celular
2.
Toxins (Basel) ; 13(11)2021 10 22.
Artículo en Inglés | MEDLINE | ID: mdl-34822532

RESUMEN

Fridericia chica (Bignoniaceae) is a traditional medicinal plant. The aim of this research was to determine the protective effects of the hydroethanolic extract from the F. chica leaves (HEFc) against the cytotoxicity of zearalenone (α-ZEL) and ß-ZEL on SH-SY5Y cells. Free radical scavenging activity of HEFc was evaluated using the DPPH method. The cytotoxicity of both zearalenone metabolites and HEFc was examined using MTT test, as was the cytoprotective effects of the HEFc on cells treated with these mycotoxins. The chemical composition of HEFc was determined using UPLC-QTOF-MS/MS. HEFc elicited good DPPH radical scavenging activity following a concentration-dependent relationship. Cells exposed to α-ZEL exhibited a viability ˂50% after 48 h of treatment (25 and 50 µM), while those exposed to ß-ZEL showed viability ˂50% (100 µM) and ˂25% (25-100 µM) after 24 and 48 h of exposure, respectively. HEFc showed a significant increase in cell viability after exposure to α-ZEL (25 and 50 µM) and ß-ZEL (6-100 µM) (p < 0.05). UPLC-QTOF-MS/MS analyses allowed the identification of 10 phytochemical components in the HEFc. In short, the hydroethanolic extract of F. chica grown in Colombian Caribbean can protect against the effects of mycotoxins and it is a valuable source of compounds with antioxidant properties.


Asunto(s)
Bignoniaceae/química , Neuroblastoma/metabolismo , Extractos Vegetales/farmacología , Sustancias Protectoras/farmacología , Zearalenona/farmacología , Línea Celular Tumoral , Humanos , Extractos Vegetales/química , Hojas de la Planta/química , Sustancias Protectoras/química
3.
Buenos Aires; MediMedia; 29 ed; 1998. 847 p.
Monografía en Español | BINACIS | ID: biblio-1192311
5.
Buenos Aires; MediMedia; 29 ed; 1998. 847 p. (83274).
Monografía en Español | BINACIS | ID: bin-83274
6.
Buenos Aires; MediMedia; 29 ed; 1998. 847 p. (68228).
Monografía en Español | BINACIS | ID: bin-68228
7.
8.
Buenos Aires; MediMedia; 29 ed; 1998. 847 p. (65576).
Monografía en Español | BINACIS | ID: bin-65576
9.
Buenos Aires; V.D.B; 1996. 1310 p. ilus. (86095).
Monografía en Español | BINACIS | ID: bin-86095

Asunto(s)
Farmacología
10.
Buenos Aires; Vademecum de Bolsillo; 27 ed; 1996. 842 p.
Monografía en Español | BINACIS | ID: biblio-1186485

Asunto(s)
Argentina , Farmacopea
11.
Buenos Aires; Vademecum de Bolsillo; 30 ed; 1996. 1310 p. tab.
Monografía en Español | BINACIS | ID: biblio-1186486

Asunto(s)
Argentina , Farmacopea
12.
Buenos Aires; V.D.B; 5 ed; 1996. 580 p.
Monografía en Español | BINACIS | ID: biblio-1187628
13.
Buenos Aires; V.D.B; 5 ed; 1996. 580 p. (59255).
Monografía en Español | BINACIS | ID: bin-59255
14.
Buenos Aires; Vademecum de Bolsillo; 30 ed; 1996. 1310 p. tab. (57723).
Monografía en Español | BINACIS | ID: bin-57723

Asunto(s)
Farmacopea , Argentina
15.
Buenos Aires; Vademecum de Bolsillo; 27 ed; 1996. 842 p. (57722).
Monografía en Español | BINACIS | ID: bin-57722

Asunto(s)
Farmacopea , Argentina
16.
Buenos Aires; Vademecum de Bolsillo; 30 ed; 1996. 1310 p. tab. (57710).
Monografía en Español | BINACIS | ID: bin-57710

Asunto(s)
Farmacopea , Argentina
17.
Buenos Aires; Vademecum de Bolsillo; 27 ed; 1996. 842 p. (57709).
Monografía en Español | BINACIS | ID: bin-57709

Asunto(s)
Farmacopea , Argentina
18.
Buenos Aires; V.D.B. SRL; 1994. 746 p. (85901).
Monografía en Español | BINACIS | ID: bin-85901
19.
Buenos Aires; V.D.B. SRL; 1994. 746 p.
Monografía en Español | BINACIS | ID: biblio-1207311

Asunto(s)
Farmacología
20.
Buenos Aires; V.D.B; 26 ed; 1995. [630] p.
Monografía en Español | LILACS-Express | BINACIS | ID: biblio-1187508
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