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[Wheat-grain moxibustion improves sleep in perimenopausal insomnia rats by regulating the SIRT1/Nrf2 signaling
Xin Li1, Sheng-Yong Su2,3, Xi Zhang4
1The First Clinical Medical College, Guangxi University of Chinese Medicine, Nanning 530001, China.
Objectives:
To observe the effect of wheat-grain moxibustion(WGM) at "Guanyuan"(CV4), "Mingmen"(GV4), and bilateral "Xuanzhong"(GB39) on the oxidative stress and pyroptosis, and the activity of the Sirtuin 1(SIRT1)/nuclear factor erythroid-2-related factor 2 (Nrf2) signaling pathway in the hypothalamus of perimenopausal insomnia (PI) rats, so as to explore its underlying mechanism in improving PI.
Methods:
Thirty-two female SD rats were randomly divided into four groups:sham, model, WGM, and WGM+EX527 (n=8 per group). The PI model was established by bilateral ovariectomy combined with an intraperitoneal injection of 4-Chloro-DL-phenylalanine suspension (350 mg/kg) for 2 consecutive days. Rats in the WGM and WGM+EX527 groups received WGM at CV4, GV4 and GB39, with 6 cones for each acupoint. The rats in the WGM+EX527 group received additional intraperitoneal injection of the SIRT1 inhibitor EX527 (10 mg/kg) 30 min before each moxibustion session. The interventions were conducted once daily for 14 consecutive days. The sleep latency and sleep duration were assessed using the pentobarbital sodium-induced sleep test (righting reflex), and the spontaneous activities (total distance moved, center zone dwelling time, and rearing times in 5 min) were measured using the open field test (OFT). The hematoxylin-eosin (H.E.) staining was used to observe morphological changes in the hypothalamic tissue. Western blot was used to detect protein expression levels of SIRT1, Nrf2, Kelch-like ECH-associated protein1 (Keap1), heme oxygenase-1 (HO-1), superoxide dismutase (SOD), catalase (CAT), NOD-like receptor thermal protein domain associated protein 3 (NLRP3), cysteingl aspartate specific protease 1 (Caspase-1), apoptosis-associated speck-like protein containing a CARD (ASC), and gasdermin-D (GSDMD) in the hypothalamus. The qPCR was used to measure mRNA expression levels of SIRT1, Nrf2, Keap1, and HO-1 in the hypothalamus. The reactive oxygen species (ROS) assay kit was used to detect ROS level of hypothalamic tissue. The ELISA was used to measure the content of interleukin (IL)-1β and IL-18 in the hypothalamus.
Results:
Compared to the sham group, the model group showed a striking decrease in the total distance traveled, central zone dwelling time and rearing times in the OFT (P<0.01), and significantly shortened sleep duration and prolonged sleep latency (P<0.01). In comparison with the model group and the WGM+EX527 group, the WGM group showed an obvious increase in the total distance traveled, central zone dwelling time and rearing times (P<0.01), and shortened sleep latency, prolonged sleep duration (P<0.01). Additionally, in comparison with the sham group, the model group had a significant down-regulation in the expression levels of hypothalamic SIRT1, Nrf2, Keap1, and HO-1 proteins and mRNAs, and SOD and CAT proteins (P<0.01), and an obvious up-regulation in the expression levels of NLRP3, Caspase-1, ASC, GSDMD proteins, ROS level, and contents of IL-1β and IL-18 (P<0.01) in the hypothalamus. In comparison with the model group and the WGM+EX527 group, both the down-regulation and up-regulation of expression levels of the proteins and mRNAs mentioned above, and ROS level and the contents of IL-1β and IL-18 were reversed in the WGM group(P<0.01, P<0.05). H.E. staining showed that in comparison with the sham group, more hypothalamic neurons were wrinkled with unclear cell structures, varying sizes and uneven distribution in the model and WGM+EX527 groups, which was alleviated in the degree of cell injury in the WGM group, for instance clearer cell structure and uniform distribution.
Conclusions:
WGM can improve the sleep and spontaneous activity of PI rats, which may be related to its functions in alleviation of hypothalamic oxidative stress and pyroptosis by regulating the SIRT1/Nrf2 signaling pathway.
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