curcumin and 2-2-bis(4-glycidyloxyphenyl)propane

Retention index (I), rather than retention factor (k), was found to be a more reasonable parameter for comparison of the relative affinity of disubstituted benzenes in MEEKC and MEKC, due to independent of I with the SDS surfactant concentration. MEKC and MEEKC may give similar or different I values, depending on types of moieties. With known I and K(ow) for alkylbenzenes as references in MEKC and MEEKC, the values of K(ow) for disubstituted benzenes can be estimated from the observed I values, where K(ow) is the octanol-water distribution constant. In addition, a group additive approach can be used to predict I for disubstituted benzenes with different moieties from the average observed I for the disubstituted benzenes with same moieties. However, electronic effects and/or intramolecular interaction may result in the different observed I from prediction.

Topics: Benzene Derivatives; Benzhydryl Compounds; Chromatography, Micellar Electrokinetic Capillary; Curcumin; Epoxy Compounds; Linear Models; Octanols; Sodium Dodecyl Sulfate; Water

The present study was undertaken to investigate the possible mechanism of curcumin-mediated beneficial effects in memory deficits associated with experimental dementia. Dementia was induced in Swiss albino mice by administering streptozotocin (3 mg kg(-1)) intracerebroventricularly on first and third day. Morris water maze test was employed to assess learning and memory of the animals. Biochemical analysis of brain homogenate was performed to assess brain acetyl cholinesterase (AChE) activity and total oxidative stress. Streptozotocin (STZ) produced a significant decrease in water maze performance of mice indicative of impairment in spatial reference memory. Curcumin (20 mg/kg p.o. daily for 14 days) successfully attenuated STZ-induced memory deficits. Higher levels of brain AChE activity and oxidative stress were observed in STZ-treated animals, which were significantly attenuated by curcumin. Furthermore, the noted beneficial effect of curcumin on STZ-induced dementia was significantly abolished by pretreatment with PPAR-gamma receptor antagonist bisphenol-A-diglycidyl ether, i.e., BADGE (30 mg/kg intraperitoneally (i.p.)). It may be concluded that the beneficial effects of curcumin are mediated through the activation of PPAR-gamma receptors.

Topics: Acetylcholinesterase; Animals; Benzhydryl Compounds; Brain; Curcumin; Dementia; Disease Models, Animal; Epoxy Compounds; Female; Male; Memory Disorders; Mice; Oxidative Stress; PPAR gamma; Streptozocin