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12,078 results on '"Yao, Jun"'

256. Indocalamus Nakai

Author

Shi, Jun Yi, Che, Bing Yin, Zhang, Yu Xiao, Zhou, De Qun, Ma, Li Sha, Yao, Jun, Shi, Jun Yi, Zhang, Yu Xiao, Zhou, De Qun, Ma, Li Sha, and Yao, Jun

Published
2022
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257. Sasa Makino et Shibata

Author

Shi, Jun Yi, Che, Bing Yin, Zhang, Yu Xiao, Zhou, De Qun, Ma, Li Sha, Yao, Jun, Shi, Jun Yi, Zhang, Yu Xiao, Zhou, De Qun, Ma, Li Sha, and Yao, Jun

Published
2022
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258. Menstruocalamus T. P. Yi

Author

Shi, Jun Yi, Che, Bing Yin, Zhang, Yu Xiao, Zhou, De Qun, Ma, Li Sha, Yao, Jun, Shi, Jun Yi, Zhang, Yu Xiao, Zhou, De Qun, Ma, Li Sha, and Yao, Jun

Published
2022
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260. Gelidocalamus T. H. Wen

Author

Shi, Jun Yi, Che, Bing Yin, Zhang, Yu Xiao, Zhou, De Qun, Ma, Li Sha, Yao, Jun, Shi, Jun Yi, Zhang, Yu Xiao, Zhou, De Qun, Ma, Li Sha, and Yao, Jun

Published
2022
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264. Sasaella Makino

Author

Shi, Jun Yi, Che, Bing Yin, Zhang, Yu Xiao, Zhou, De Qun, Ma, Li Sha, Yao, Jun, Shi, Jun Yi, Zhang, Yu Xiao, Zhou, De Qun, Ma, Li Sha, and Yao, Jun

Published
2022
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265. Pleioblastus Nakai

Author

Shi, Jun Yi, Che, Bing Yin, Zhang, Yu Xiao, Zhou, De Qun, Ma, Li Sha, Yao, Jun, Shi, Jun Yi, Zhang, Yu Xiao, Zhou, De Qun, Ma, Li Sha, and Yao, Jun

Published
2022
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266. Pseudosasa Makino ex Nakai

Author

Shi, Jun Yi, Che, Bing Yin, Zhang, Yu Xiao, Zhou, De Qun, Ma, Li Sha, Yao, Jun, Shi, Jun Yi, Zhang, Yu Xiao, Zhou, De Qun, Ma, Li Sha, and Yao, Jun

Published
2022
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267. Fargesia Franchet

Author

Shi, Jun Yi, Che, Bing Yin, Zhang, Yu Xiao, Zhou, De Qun, Ma, Li Sha, Yao, Jun, Ye, Xia Ying, Shi, Jun Yi, Zhang, Yu Xiao, Zhou, De Qun, Ma, Li Sha, and Yao, Jun

Published
2022
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270. Yushania P. C. Keng

Author

Shi, Jun Yi, Che, Bing Yin, Zhang, Yu Xiao, Zhou, De Qun, Ma, Li Sha, Yao, Jun, Zhang, Xian Zhi, Shi, Jun Yi, Zhang, Yu Xiao, Zhou, De Qun, Ma, Li Sha, and Yao, Jun

Published
2022
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271. Chimonocalamus Hsueh et T. P. Yi

Author

Shi, Jun Yi, Che, Bing Yin, Zhang, Yu Xiao, Zhou, De Qun, Ma, Li Sha, Yao, Jun, Zhang, Xian Zhi, Shi, Jun Yi, Zhang, Yu Xiao, Zhou, De Qun, Ma, Li Sha, and Yao, Jun

Published
2022
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272. Drepanostachyum P. C. Keng

Author

Shi, Jun Yi, Che, Bing Yin, Zhang, Yu Xiao, Zhou, De Qun, Ma, Li Sha, Yao, Jun, Zhang, Xian Zhi, Shi, Jun Yi, Zhang, Yu Xiao, Zhou, De Qun, Ma, Li Sha, and Yao, Jun

Published
2022
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273. Thamnocalamus Munro

Author

Shi, Jun Yi, Che, Bing Yin, Zhang, Yu Xiao, Zhou, De Qun, Ma, Li Sha, Yao, Jun, Zhang, Xian Zhi, Shi, Jun Yi, Zhang, Yu Xiao, Zhou, De Qun, Ma, Li Sha, and Yao, Jun

Published
2022
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277. Mining Area Environment

Author

Deng, Jiushuai, Peng, Suping, Wang, Liang, Bi, Yinli, Yao, Jun, Wang, Qiongjie, Deng, Jiushuai, Peng, Suping, Wang, Liang, Bi, Yinli, Yao, Jun, and Wang, Qiongjie

Published
2022
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279. Resource Development Methods

Author

Deng, Jiushuai, Peng, Suping, Wang, Liang, Bi, Yinli, Yao, Jun, Wang, Qiongjie, Deng, Jiushuai, Peng, Suping, Wang, Liang, Bi, Yinli, Yao, Jun, and Wang, Qiongjie

Published
2022
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280. Related Knowledge

Author

Deng, Jiushuai, Peng, Suping, Wang, Liang, Bi, Yinli, Yao, Jun, Wang, Qiongjie, Deng, Jiushuai, Peng, Suping, Wang, Liang, Bi, Yinli, Yao, Jun, and Wang, Qiongjie

Published
2022
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282. Introduction

Author

Deng, Jiushuai, Peng, Suping, Wang, Liang, Bi, Yinli, Yao, Jun, Wang, Qiongjie, Deng, Jiushuai, Peng, Suping, Wang, Liang, Bi, Yinli, Yao, Jun, and Wang, Qiongjie

Published
2022
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284. Descending serotonergic modulation from rostral ventromedial medulla to spinal trigeminal nucleus is involved in experimental occlusal interference-induced chronic orofacial hyperalgesia

Author

Si-Yi Mo, Yang Xue, Yuan Li, Yao-Jun Zhang, Xiao-Xiang Xu, Kai-Yuan Fu, Barry J. Sessle, Qiu-Fei Xie, and Ye Cao

Subjects
Pain modulation, Serotonin, Rostral ventromedial medulla, Chronic primary myofascial orofacial pain, Experimental occlusal interference, Hyperalgesia, Medicine
Abstract

Abstract Background Dental treatment associated with unadaptable occlusal alteration can cause chronic primary myofascial orofacial pain. The serotonin (5-HT) pathway from the rostral ventromedial medulla (RVM) exerts descending modulation on nociceptive transmission in the spinal trigeminal nucleus (Sp5) and facilitates chronic pain. The aim of this study was to investigate whether descending 5-HT modulation from the RVM to the Sp5 is involved in the maintenance of primary myofascial orofacial hyperalgesia after persistent experimental occlusal interference (PEOI) or after delayed removal of experimental occlusal interference (REOI). Methods Expressions of 5-HT3A and 5-HT3B receptor subtypes in the Sp5 were assessed by immunofluorescence staining and Western blotting. The release and metabolism of 5-HT in the Sp5 were measured by high-performance liquid chromatography. Changes in the pain behavior of these rats were examined after specific pharmacologic antagonism of the 5-HT3 receptor, chemogenetic manipulation of the RVM 5-HT neurons, or selective down-regulation of 5-HT synthesis in the RVM. Results Upregulation of the 5-HT3B receptor subtype in the Sp5 was found in REOI and PEOI rats. The concentration of 5-HT in Sp5 increased significantly only in REOI rats. Intrathecal administration of Y-25130 (a selective 5-HT3 receptor antagonist) dose-dependently reversed the hyperalgesia in REOI rats but only transiently reversed the hyperalgesia in PEOI rats. Chemogenetic inhibition of the RVM 5-HT neurons reversed the hyperalgesia in REOI rats; selective down-regulation of 5-HT in advance also prevented the development of hyperalgesia in REOI rats; the above two manipulations did not affect the hyperalgesia in PEOI rats. However, chemogenetic activation of the RVM 5-HT neurons exacerbated the hyperalgesia both in REOI and PEOI rats. Conclusions These results provide several lines of evidence that the descending pathway from 5-HT neurons in the RVM to 5-HT3 receptors in the Sp5, plays an important role in facilitating the maintained orofacial hyperalgesia after delayed EOI removal, but has a limited role in that after persistent EOI. Graphical Abstract

Published
2023
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285. Design of functional vancomycin-embedded bio-derived extracellular matrix hydrogels for repairing infectious bone defects

Author

Dong Qi, Chen Sunfang, Zhou Jiuqin, Liu Jingcheng, Zou Yubin, Lin Jiawei, Yao Jun, Cai Dan, Tao Danhua, Wu Bing, and Fang Bin

Subjects
infectious bone defects, decellularized periosteum matrix hydrogel, anti-microbial, Technology, Chemical technology, TP1-1185, Physical and theoretical chemistry, QD450-801
Abstract

The treatment of infectious bone defects has become a troublesome issue in orthopedics. The disease requires effective anti-infective and bone-reconstruction therapeutic functionalities. In this study, we prepared a novel antibacterial material (vancomycin-impregnated periosteal extracellular matrix [Van-PEM]) by embedding vancomycin in a periosteal extracellular matrix (PEM)-derived hydrogel via physical stirring for the treatment of infectious bone defects. The microstructure, porosity, degradation, and release properties of this antibacterial hydrogel were characterized. The in vitro hemolytic reaction, cytotoxicity, osteogenic ability, and antibacterial properties were also carefully studied. The results showed that the Van-PEM hydrogel possessed a fibrous network structure with high porosity. Moreover, the hydrogel demonstrated slow degradation in vitro and could release vancomycin for at least 1 week. The hydrogel showed no cytotoxicity and possessed good biocompatibility with blood cells. It also promoted osteogenesis and exerted a significant bactericidal effect. Subsequently, the anti-infection and bone-healing abilities of the antibacterial hydrogel were investigated in a rat model of infectious calvarial defects, and the infectious skull defect was successfully cured in vivo. Therefore, Van-PEM hydrogels may represent a promising therapeutic approach for treating infectious bone defects.

Published
2023
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