Table 1.
Experimental model | Effect | Ref. | |
---|---|---|---|
Crocin | Rat | Protected neurons against chronic stress damages via reducing MDA level as well as elevating the levels of GPx, GR, SOD and total antioxidant capacity | [11] |
PC-12 cell | Protected PC-12 cell against oxidative stress induced by deprived from serum/glucose against via preventing membrane lipid peroxidation | [12] | |
Protected PC-12 cell against ischemic stress-induced neural cell death via increasing GSH content and blocking the activation of JNK pathways | [13] | ||
Protected PC-12 cell against ACR induced neural cell death via blocking down-regulation of Bcl-2, up-regulation of Bax as well as decreasing apoptosis and ROS generation in the treated cells | [14] | ||
Rat | Protected hippocampus against chronic stress induced learning and memory loss by modulating oxidative stress | [15] | |
Protected brain against acute swimming exercise induced oxidative stress by enhancing antioxidant activity and decreasing the levels of XO and MDA | [16] | ||
Protected brain against haloperidol-induced orofacial dyskinesia by increasing GSH and decreasing MDA | [17] | ||
Cultured rat microglial cells | Protected microglial cells against LPS-induced neuroinflammation by inhibiting NF-κB activation, the levels of NO, TNF-α, IL-1β, and ROS | [22] | |
Protected microglial cells against TNF-α-induced neuroinflammation by blocking the expression of Bcl-XS and LICE and ameliorating the Bcl-XL mRNA expression | [23] | ||
Retinal ganglion & BV2 cells | Protected retinal ganglion cells against LPS-induced microglial activation and progression of glaucoma by decreasing the expression of microglial markers (CD11b and Iba-1) and pro-inflammatory mediators (iNOS, COX-2, IL-1β, and TNF-α). Suppressing CX3CR1 expression by modulating NF-κB/YY1 signaling | [24] |
Abbreviations: MDA: malondialdehyde, GPx: glutathione peroxidase, GR: glutathione reductase, SOD: superoxide dismutase, GSH: glutathione peroxidase, JNK: c-Jun NH2-terminal kinases, ACR: acrylamide, ROS: reactive oxygen species, XO: xanthine oxidase, LPS: lipopolysaccharide, NO: nitric oxide, TNF: tumor necrosis factor alpha, IL-1β: interleukin-1β, NOs: nitric oxide synthase, COX-2: cyclooxygenase-2, NF-Κb: Nuclear factor-κB.