2019
DOI: 10.1097/wnr.0000000000001302
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Ginsenoside Rg1 attenuates chronic unpredictable mild stress-induced depressive-like effect via regulating NF-κB/NLRP3 pathway in rats

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Cited by 28 publications
(25 citation statements)
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“…The CUMS model was established referring to previous studies [ 20 23 ] that evaluate biological effects of antidepressants. Except for the control group, the remaining 60 rats underwent a 21-day CUMS procedure modified on Zhang et al [ 24 ], during which the rats were exposed to different stressors including water deprivation (24 h), food deprivation (24 h), immobilization (2 h), level shaking (5 min), and tail clamping (3 min; 3 cm from the end of the tail). These stressors were processed randomly as one stressor per day on rats, and the same stressor was not applied consecutively over two days to avoid animals' prediction of the occurrence of stimulation ( Table 1 ).…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…The CUMS model was established referring to previous studies [ 20 23 ] that evaluate biological effects of antidepressants. Except for the control group, the remaining 60 rats underwent a 21-day CUMS procedure modified on Zhang et al [ 24 ], during which the rats were exposed to different stressors including water deprivation (24 h), food deprivation (24 h), immobilization (2 h), level shaking (5 min), and tail clamping (3 min; 3 cm from the end of the tail). These stressors were processed randomly as one stressor per day on rats, and the same stressor was not applied consecutively over two days to avoid animals' prediction of the occurrence of stimulation ( Table 1 ).…”
Section: Methodsmentioning
confidence: 99%
“…The whole intervention lasted for 14 days after CUMS modeling [ 24 ]. After CUMS modeling, rats in the EA group underwent EA at GV20 (at the midpoint between the auricular apices) and GV29 (at the midpoint between the medial ends of the two eyebrows) [ 26 ].…”
Section: Methodsmentioning
confidence: 99%
“…Stressful situations modulate serotonergic and dopaminergic neurotransmission in animal models of depression, as well as eating behavior (Gamaro, Manoli, Torres, Silveira, & Dalmaz, 2003). Although, weight gain is a physical sign of the effect of chronic stress (Nollet, Guisquet, & Belzung, 2013), some studies reported a decline in the rate of body weight gain in unpredictable chronic mild stress animals (Kaster et al., 2015; Nollet et al., 2011; Zhang et al., 2019), and others have been unable to detect differences in this parameter (Li et al., 2007; Yalcin, Belzung, & Surget, 2008). Herein, we demonstrated a reduction in body‐weight gain in CUS mice, which was related to depressive phenotype.…”
Section: Discussionmentioning
confidence: 99%
“…Animals were randomly divided into six groups as follows: control/vehicle (water), control/fluoxetine (20 mg/kg), control/extract (200 mg/kg), CUS/vehicle, CUS/fluoxetine (20 mg/kg), and CUS/extract (200 mg/kg). The CUS procedure was performed according to a method described previously (Kaster et al., 2015; Liang et al., 2012; Zhang, Wang, Xue, Gao, & Li, 2019).…”
Section: Methodsmentioning
confidence: 99%
“…However, through the study of the effective molecular structures of the nine components of JZG, it is not difficult to determine that the effective molecules in JZG play active roles in the treatment of depression through various pathways. Ginsenoside can lessen unpredictable mild stress and depression-like effects by regulating the NF-κ B/NLRP3 pathway in a rat model; 136 ginsenoside may also protect depression-like behavior by inhibiting glial activation, synaptic damage, and neuronal apoptosis. 137 Schisandrin protects depression-like behaviors caused by chronic unpredictable mild stress through GDNF/ERK1/2/ ROS and PI3K/AKT/NOX signaling pathways.…”
Section: The Pharmacological Mechanism Of Jzg In the Treatment Of Depmentioning
confidence: 99%