2005
DOI: 10.1007/s11010-005-7637-1
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Cytoprotective and antioxidant activity of Rhodiola imbricata against tert-butyl hydroperoxide induced oxidative injury in U-937 human macrophages

Abstract: The present study reports cytoprotective and antioxidant activity of aqueous and alcoholic extracts of Rhodiola imbricata rhizome on tert-butyl hydroperoxide (tert-BHP) induced cytotoxicity in U-937 human macrophages. There was an increase in cytotoxicity and apoptosis significantly in the presence of tert-BHP over control cells. The tert-BHP induced cytotoxicity can be attributed to enhanced reactive oxygen species (ROS) production which in turn is responsible for fall in reduced glutathione (GSH) levels; fur… Show more

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Cited by 95 publications
(42 citation statements)
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“…1a), has been documented to possess neuroprotective effects against neuronal damage induced by various insults. [19][20][21][22][23][24][25][26][27][28][29][30][31][32][33] However, the underlying mechanisms are still not well understood.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…1a), has been documented to possess neuroprotective effects against neuronal damage induced by various insults. [19][20][21][22][23][24][25][26][27][28][29][30][31][32][33] However, the underlying mechanisms are still not well understood.…”
Section: Discussionmentioning
confidence: 99%
“…11,12) Salidroside (SA), a natural compound from Rhodiola rosea L., is a major active ingredient responsible for most pharmacological effects of Rhodiola, such as anti-oxidative, anti-aging, anti-inflammatory, anti-cancer, anti-fatigue and anti-depressant activities. [13][14][15][16][17][18][19] Increasing evidence suggests that SA may have neuroprotective effects in injured brain. SA can reduce the degree of cerebral edema and the brain infarct size of rats with global cerebral ischemia, relieve the metabolism abnormity of free radicals and improve the function of cognition as well as behavioral and histological outcomes.…”
mentioning
confidence: 99%
“…RI1, RI3, and RI7 at 15 ± 2°Cand 25± 2°C. Shoot multiplication was observed earlier at 15 ± 2°C (18)(19)(20)(21)(22)(23) days) compared to 25± 2°C (25-30 days). Also, at 15 ± 2°C, number and length of shoots were found to be much higher (Graph 1).The MS medium supplemented with BAP (1 mg/l) + KN (2 mg/l) was found to be the best for the multiplication of shoots in 18 -23 days with …”
Section: Direct Shoot Organogenesis and Multiplicationmentioning
confidence: 87%
“…Se evaluaron cuatro concentraciones de los extractos, siendo la máxima CC 50 la obtenida en los ensayos de citotoxicidad para la misma línea celular (cuadro 2). Se colocaron 150.000 células en contacto con los tratamientos y controles (28)(29). Como control negativo se utilizó DMSO al 0,5 % y, como controles positivos, peróxido de hidrógeno (H 2 O 2 ) a 100 µM sin activación metabólica (fracción S9) y 2-aminofluoreno, a 1 µM, para la activación metabólica.…”
Section: Determinación Del Efecto Genotóxicounclassified
“…Los tratamientos se incubaron durante una a tres horas y se midió la viabilidad de las células después del tratamiento (28)(29)(30). Se tomaron 20 µl de las células, las cuales se mezclaron con 80 µl de agarosa de bajo punto de fusión (0,5 %) y la mezcla se colocó en placas portaobjetos, previamente impregnadas con agarosa de punto de fusión normal (1 %).…”
Section: Determinación Del Efecto Genotóxicounclassified