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Pharmacological characterization To examine whether the potent weight loss observed in vivo after GLP-1MK-801 treatment is attributable to pharmacological synergy between GLP-1 and MK-801 or consequential to altered pharmacokinetic properties of the parent GLP-1 analogue, we designed and synthesized a conjugate comprising an inactive MK-801 surrogate 22 (Supplementary Fig

Administration of luteolin (80 mg/kg/day) resulted in a significant reduction in the activation of p-JNK, p38 MAPK, GFAP, Iba-1, and various inflammatory markers such as p-NF-B p65, tumor necrosis factor-alpha (TNF-), interleukin-1 beta (IL-1), a decrease in pro-apoptotic proteins (including Bax, Caspase-3, Cox-2), a downregulation of BACE-1 and A1-42 concentrations, and an enhancement of synaptic markers (namely PSD-95, SNAP-25)

Epilepsia 51 (6), 10691077 (2010)