The neuroprotective effects of Herba siegesbeckiae extract on cerebral ischemia/reperfusion in rats
- Author:
Hui-Ling WU
1
;
Qing-Qing WU
1
;
Jing-Quan CHEN
1
;
Bin-Bin ZHOU
1
;
Zheng-Shuang YU
1
;
Ze-Lin YANG
1
;
Wen-Fang LAI
1
;
Gui-Zhu HONG
1
Author Information
- Publication Type:Journal Article
- Keywords: apoptosis; cerebral is-chemia/reperfusion; Herba siegesbeckiae extract; mNSS score; NeuN; neuroprotection
- From: Chinese Pharmacological Bulletin 2024;40(1):70-75
- CountryChina
- Language:Chinese
- Abstract: Aim To study the neuroprotective effects of Herba siegesbeckiae extract on cerebral ischemia/ reperfusion rats and its mechanism. Methods Sixty SD rats were randomly divided into model group, low, middle and high dose groups of Herba siegesbeckiae, and Sham operation group, and the drug was given continuously for seven days. The degree of neurologic impairment was evaluated by mNSS, and the infarct volume was measured by MRI. The number of Nissl-posi- tive cells was detected by Nissl staining, and the apop- tosis was accessed by Tunel staining. Furthermore, the expression of Bax, Bcl-2 and NeuN was observed by Western blot, and the expression of NeuN was detected by immunofluorescence staining. The expression of IL- 1β, TNF-α and IL-6 mRNA was performed by RT- qPCR. Results The mNSS score and the volume of ischemic cerebral infarction in the model group were significantly increased, and Herba siegesbeckiae extract treatment significantly decreased the mNSS score and infarct volume (P<0.05, P<0.01). Herba siegesbeckiae extract could increase the number of Nissl-pos- itive cells and the expression of NeuN (P<0.01), and reduce the number of Tunel-positive cells (P<0.01). Western blot showed that Herba siegesbeckiae extract inhibited the expression of Bax, increased Bcl-2 and NeuN in ischemic brain tissue (P<0.01). RT-qPCR showed that Herba siegesbeckiae extract inhibited the expression of IL-1 β, TNF-α and IL-6 mRNA in the is-chemic brain tissue (P<0.01). Conclusions Herba siegesbeckiae extract can reduce the cerebral infarction volume, improve the neurological function damage, inhibit the apoptosis of nerve cells and the expression of inflammatory factors and promote the expression of NeuN, there by exerting protective effects on MCAO rats.
