1.Bilateral laryngeal granulomas after endotracheal intubation.
Zhi-hong LIN ; Hua-lin WANG ; Hui-e WANG
Chinese Journal of Otorhinolaryngology Head and Neck Surgery 2007;42(1):67-68
Adult
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Aged
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Female
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Granuloma, Laryngeal
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etiology
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Humans
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Intubation, Intratracheal
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adverse effects
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Male
4.Infantile kala-azar: report of a case.
Zhi-gang LIU ; Xiao-jie LIN ; Xiao-hong LIU
Chinese Journal of Pediatrics 2008;46(3):238-238
6.Clinical significance of detection of tumor suppressor genes aberrant methylation in cervical carcinoma tissue
Jun XU ; Hong-Lin WANG ; Gao-Chuan LU ; Zhi-Jie WANG ; Xiao LIN ; Hong-Wei ZHOU ;
Chinese Journal of Obstetrics and Gynecology 2001;0(06):-
0.05).(4) Significant differences between CC and CIN Ⅰ for p16,CDH1,RASSF1A and TIMP3 genes(P
8.Study on chemical constituents from cultivated Gynura nepalensis.
Yao LU ; Zhi-Hong LI ; Lin MA ; An-Jun DENG ; Feng WU ; Zhi-Hui ZHANG ; Hai-Lin QIN
China Journal of Chinese Materia Medica 2014;39(19):3777-3781
Taking application of some isolation and purification technologies, such as solvent extraction, preliminary solvent isolation, column chromatographies over silica gel and Sephadex LH-20 gel and preparative HPLC, 10 compounds were obtained from Gynura nepalensis cultivated in the suburban area of Beijing. Their structures were identified by spectroscopic methods and comparison with literature as (3R) -3-hydroxy-β-ionone (1), (3S,5R, 6S, 7E) -5, 6-epoxy-3-hydroxy-7-megastigmen-9-one (2), (+) -boscialin (3), 3, 6-trans-3-hydroxy-α-ionone (4), 3, 6-cis-3-hydroxy-α-ionone (5), 3, 4-cis-3, 4-dihydroxy-β-ionone (6), ethyl caffeate (7), loliolide (8), 1H-indole-3-carbaldehyde (9), and 3-(hydroxyacetyl)indole (10), respectively. All compounds were isolated from the title plant for the first time, and with compounds 1, 2, 4-7, 9 and 10 being isolated from Gynura species for the first time. Structurally, the above compounds 1-6 belong to C13 nor-sesquiterpenoids, sharing the same carbon skeleton of megastigmane. According to this study, they are one of major kinds of chemical constituents of Gynura nepalensis and have important reference value for the investigation on phytotaxonomy of this species.
Asteraceae
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chemistry
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Caffeic Acids
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chemistry
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Cyclohexanones
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Drugs, Chinese Herbal
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chemistry
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Glucosides
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Indoles
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chemistry
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Mass Spectrometry
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Molecular Structure
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Norisoprenoids
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chemistry
9.Fingerprint and spectrum-effect relationships on Tripterygium glycosides preparation.
Jie CHI ; Bing LIN ; Zhi-hong LIU ; Li-na YANG ; Xue-mei LIU ; Hong-tao SONG
China Journal of Chinese Materia Medica 2015;40(8):1479-1483
Tripterygium glycosides preparation which extracted from the traditional Chinese herb Tripterygium wilfordii (TWHY), was widely used to treat the autoimmune diseases. Previous works demonstrated that TWHF had potent anti-inflammatory and immunosuppressive properties. But the different quality and high incident rate of side effects of different manufactures inhibited its clinical application. Since TWHF had been generally known to play a therapeutical effect by synergism of multiple constituents, it was necessary to build the relationship between the HPLC fingerprint and bioactivity so as to ensure the quality safety and efficacy. The HPLC fingerprint showed that description and content of peaks from different manufactures were diverse. Only 11 common peaks were found. In this study, mice spleen cells stimulated by Con A were used to test the proliferation inhibition bioactivity of TWHF preparations, which were incubated with 30, 15, 7.5, 3.75, 1.88 and 0.94 mg x L(-1) TWHF preparations for 48 h. The results showed that mice spleen cells proliferation was inhibited by all TWHF preparations significantly compared with the control group, which suggested the TWHF preparations showed immune suppress activity. The TWHF preparations from 7 manufacture showed different IC50 value, which might belong to different contents which showed in the HPLC fingerprint. Moreover, a relationship between the HPLC fingerprint and the bioactivity were established to identify important constituents by grey relational analysis (GRA). The result showed that all the contents were relative with the IC50, especially No. 5 and 10 peaks, but No. 1 peak, which was proved to be triptolide, had few contribute to the inhibition of mice spleen cells proliferation. The study of relationship between the HPLC fingerprint and the IC50 by GRA could help to investigate mechanism of bioactive and provide an evidence for the quantification of multi-constituents.
Animals
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Anti-Inflammatory Agents
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analysis
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pharmacology
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Cell Proliferation
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drug effects
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Chromatography, High Pressure Liquid
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Drugs, Chinese Herbal
;
analysis
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pharmacology
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Glycosides
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analysis
;
pharmacology
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Male
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Mice
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Mice, Inbred BALB C
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Spleen
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cytology
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drug effects
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Tripterygium
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chemistry
10.Impact of cell transplantation on glutamate and dopamine in the rat striatum
Ling LIN ; Yu-Hong ZHENG ; Zhi-Hong ZHENG
Chinese Journal of Neuromedicine 2008;7(11):1127-1130
Objective To investigate the impact of anesthetization and manipulation on neurotransmitters glutamate and dopamine during cell transplantation. Methods Neural stem cells cultured in vitro from postnatal rats were implanted into the striatum of normal adult rats. Brain microdialysis combined with high-performance liquid chromatography (HPLC) was applied to dynamically detect the impact of microdialysis probe implantation, anesthetics ketamine and pentobarbital and implanted cells etc on glutamate and dopamine levels. Results After 15 min probe implantation into the rat striatum, glutamate and dopamine levels in the striatum increased, evidently higher than the baseline value and declined to the baseline level within about 5-6 h. Ketamine and pentobarbital anesthetization for 15 rain resulted in a transient increase in glutamate and dopamine levels in the rat striamm;there were no significant effects on in vivo glutamate and dopamine levels by cell implantation itself. Conclusion Routine doses of intraperitoneal ketamine or pentobarbital anesthetization may result in a transient increase in glutamate and dopamine levels within the brain extracellular space. Based on these data, the optimal time for commencing brain microdialysis on glutamate and dopamine should be at least 6 h after probe implantation.