AIM: To study the influence of ginkgolides on expression of inducible nitric oxide synthase (iNOS) in rats. METHODS: Middle cerebral artery occlusion(MCAO) model was induced by ligating internal carotid artery of Sprague Dawley(SD) rats.In this model,the behavioral deficits performance of SD rats was analyzed after given ginkgolides and nimo dipin, respectively, and iNOS gene expression changes in MCAO group were investigated. RESULTS:The expression of iNOS was increased in MCAO models and inhibited in ginkgolides groups. CONCLUSION:Ginkgolides have inhibitive efficacy of iNOS on cerebral ischemia and can reduce brain damage.

OBJECTIVE:To work out the quality control standard of Penqiangyan tablets.METHODS:The major herbs in the preparation were identified by TLC.The contents of total ferulic acid in Radix Angelia Sinensis and Rhizoma Chuanxiong were determined by HPLC.RESULTS:Ferulic acid had a good linearity in the range of1.244～124.4?g/ml(r=0.9984).The recovery and RSD were97.06%and1.44%(n=6)respectively.CONCLUSION:The method is simple and feasible and had a good repeatability.It can be used for the quality control of Penqiangyan tablets.

To investigate the active compounds from on the heart and brain of mice at simulated high altitude.Fifty healthy male adult BALB/c mice were randomly divided into normal control group, hypoxic model group, acetazolamide group, petroleum ether extract of (PESI) group and octacosan group with 10 mice in each group. Acetazolamide group, PESI group and octacosan group were treated with acetazolamide PESI (200 mg/kg) or octacosan by single tail vein injection, respectively. Except normal control group, the mice were exposed to a simulated high altitude of for in an animal decompression chamber. After the mice were sacrificed by cervical dislocation, the heart and brain were histologically observed by HE staining; superoxide dismutase (SOD) activity, total anti-oxidant capacity (T-AOC) and the content of malondialdehyde (MDA) in plasma, heart and brain tissues were detected by WST-1 method, ABTS method and TBA method, respectively; lactic acid and lactate dehydrogenase (LDH) activity in plasma, heart and brain tissues were detected by colorimetric method and microwell plate method, respectively; ATP content and ATPase activity in heart and brain tissues were detected by colorimetric method. PESI and octacosane significantly attenuated the pathological damages of heart and brain tissue at simulated high altitude; increased SOD activity, T-AOC and LDH activity, and decreased the contents of MDA and lactic acid in plasma, heart and brain tissues; increased the content of ATP in heart and brain tissues; increased the activities of Na-K ATPase, Mg ATPase, Ca ATPase and Ca-Mg ATPase in myocardial tissue; and increased the activities of Mg ATPase, Ca-Mg ATPase in brain tissue. PESI and octacosan exert anti-hypoxic activity by improving the antioxidant capacity, reducing the free radical levels, promoting the anaerobic fermentation, and alleviating the energy deficiency and metabolic disorders caused by hypoxia in mice.
Altitude ; Animals ; Brain/metabolism* ; Heart ; Male ; Malondialdehyde ; Mice ; Mice, Inbred BALB C ; Superoxide Dismutase/metabolism*

ObjectiveTo explore the regulatory mechanism of hypoxia exposure on carbon metabolism pathway in spleen of mice. MethodsC57BL/6 mice were raised at altitudes of 400 m and 4 200 m， with 5 mice in each group. After 30 days， spleen tissues were aseptically removed for analysis of differentially expressed genes， proteins， and metabolites using transcriptome sequencing， proteomics， and non-targeted metabolomics. GO and KEGG enrichment analysis were conducted to explore key pathways. The key genes and protein in the pathway were validated by RT-qPCR and Western blot. ResultsTranscriptome sequencing revealed a significant difference in the expression of 4 213 genes in hypoxic exposure， of which 1 947 were up-regulated and 2 266 were down-regulated. The analysis of differentially expressed proteins showed that 166 proteins were up-regulated and 39 proteins were down-regulated. The results of non-targeted metabolomics showed that 133 different metabolites were screened under high altitude hypoxia condition， of which 95 were up-regulated and 38 were down-regulated. KEGG enrichment analysis showed that differentially expressed genes， differentially expressed proteins and differentially expressed metabolites were enriched into the carbon metabolic pathway. Therefore， the key genes and proteins in the carbon metabolic pathway were verified. The mRNA and protein expressions of PGAM2、ENO3、PRPS2、PGLS、RPE、IDH3A、SUCLA2 and MDH2 were significantly down-regulated in the carbon metabolism pathway. ConclusionLow oxygen environment at high altitude weakens glycolysis， tricarboxylic acid cycle and pentose phosphate pathway by inhibiting the carbon metabolism pathway of the body， resulting in oxidative stress and energy metabolism imbalance.

Antiviral Agents/pharmacology* ; COVID-19 ; Coronavirus 3C Proteases ; Humans ; Lactams ; Leucine ; Molecular Docking Simulation ; Molecular Dynamics Simulation ; Nitriles ; Proline ; Protease Inhibitors/pharmacology* ; SARS-CoV-2