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1.
Chinese journal of integrative medicine ; (12): 737-743, 2021.
Article in English | WPRIM | ID: wpr-922117

ABSTRACT

OBJECTIVE@#To explore the effect of electro-acupuncture (EA) on glucose and lipid metabolism in unmarried patients with polycystic ovary syndrome (PCOS).@*METHODS@#Fifty-four PCOS patients were equally randomized into true acupuncture group and sham acupuncture group (control) for totally 16 weeks of treatment by random method with a computerized randomization program. Patients in true acupuncture group accepted traditional acupuncture methods with EA and two sets of acupoint groups were used alternatively. The first set consisted of Zhongji (CV 3), Qihai (CV 6), Guilai (ST 29), Sanyinjiao (SP 6), Yinlingquan (SP 9), Hegu (LI4) and Baihui (GV 20), and the second set consisted of Tianshu (ST 25), ST 29, CV 3, CV 6, SP 6, Taichong (LR 3), Neiguan (PC) 6 and GV 20. Patients in the sham acupuncture group accepted shallow acupuncture methods through EA without electricity at 4 non-meridian points in each shoulder and upper arm. Outcome measures included body mass index (BMI), waist-hip-ratio (WHR), oral glucose tolerance test (OGTT), insulin release test, glucose and lipid metabolism indicators such as total cholesterol (TC), triglycerides, high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol, adiponectin, leptin, visfatin, resistin, and interleukin (IL-6).@*RESULTS@#Twenty-six subjects in the true acupuncture group and 20 subjects in the sham group completed the clinical trial. After 16 weeks of treatment, no significant difference in the outcome measures were observed between the two groups (P>0.05). However, as compared with baseline data, a reduction in weight, BMI, hipline, WHR, fasting glucose, homeostatic model assessment of insulin sensitivity, visfatin and HDL-C, and an increase in resistin and IL-6 were observed in the true acupuncture group (P<0.05). In addition, a reduction in visfatin and an increase in TC were also observed in the sham group (P<0.05).@*CONCLUSIONS@#Acupuncture may have a beneficial effect in the treatment of PCOS by improving glucose and lipid metabolism. Moreover, the sham acupuncture may be not completely ineffective. Sham acupuncture may improve some of the aspects of the glucose and lipid metabolism of PCOS patients through a placebo effect. (Registration Nos. ChiCTR-TRC-12002529 and NCT01812161).


Subject(s)
Female , Humans , Acupuncture Therapy , Glucose , Insulin Resistance , Lipid Metabolism , Polycystic Ovary Syndrome/therapy , Single Person
2.
Acta Pharmaceutica Sinica ; (12): 21-27, 2015.
Article in Chinese | WPRIM | ID: wpr-251823

ABSTRACT

To investigate the effect of huangqin tang on expression of cytokines and NF-κB p65 in rats with ulcerative colitis (UC), and to probe into its underlying mechanisms of action. The mode of UC rats with cell immunoreactivity was made using compound method (trinitrobenzene sulfonic acid and ethanol). Rats were randomly divided into control group, model group, SASP group and high dose, middle dose and low dose of huangqin tang group. The food intake, body weight and microscopic damage of rats in each group were evaluated after being treated for five days. The blood and colon tissue were also collected. Production of NO was detected by Griess assay, the expression levels of IL-6, TNF-α, PGE2 were detected by ELISA. ICH method was undertaken to determine the expression of NF-κB p65 protein in colon tissue. The food intake and body weight of model group rats were lower than that of control group. The expression levels of NO, IL-6, TNF-α, PGE2 in serum and NF-κB p65 protein of colon tissue in model group were higher than that of control group. The above indexes were ameliorated in high and middle dose of huangqin tang groups. But there was no significant difference with SASP group. NF-κB p65 may be involved in the pathogenesis of UC, and huangqin tang can inhibit the relative activity of NF-κB p65, and decrease the expression levels of NO, IL-6, TNF-α and PGE2.


Subject(s)
Animals , Rats , Colitis, Ulcerative , Metabolism , Dinoprostone , Blood , Drugs, Chinese Herbal , Pharmacology , Interleukin-6 , Blood , Nitric Oxide , Blood , Random Allocation , Rats, Sprague-Dawley , Signal Transduction , Transcription Factor RelA , Metabolism , Tumor Necrosis Factor-alpha , Blood
3.
Acta Pharmaceutica Sinica ; (12): 1418-1425, 2014.
Article in Chinese | WPRIM | ID: wpr-299118

ABSTRACT

The pharmacodynamic (PD) and pharmacokinetic (PK) properties of Huangqin Tang (HQT) were investigated in yeast-induced febrile rats. Blood sample and rectal temperature data of the rats were collected at different times after single oral administration of HQT at 20 g x kg(-1). The plasma concentrations of paeoniflorin, baicalin, wogonoside, baicalein, wogonin, oroxylin A, glycyrrhizic acid and glycyrrhetinic acid were quantified by a sensitive liquid chromatography-tandem mass spectrometric (LC-MS) method. The blood concentrations of PGE2, 1L-1β and TNF-α were detected by radioimmunoassay (RIA). All pharmacokinetic parameters were processed by non-compartmental analysis using WinNonlin software. The potential relationship between the mean concentration of eight constituents and the antifebrile efficacy was investigated by calculating Pearson correlation coefficients. It was found that HQT had significant antifebrile efficacy in yeast-induced febrile rats, but had no effect to normal rats. The antifebrile effect of HQT can be attributed to the inhibition of PGE2, 1L-1β and TNF-α. The constituents (baicalin, wogonoside, baicalein, wogonin, oroxylin A, glycyrrhizic acid and glycyrrhetinic acid) in febrile rats had delayed absorption and elimination, a longer residence time in the body, and higher C(max) and AUC than those in normal rats. Febrile condition could affect the pharmacokinetic behaviour of HQT in vivo; the flavonoids with the same backbone showed the similar fate in the body; baicalein and wogonin had a strong positive correlation (R > 0.66, P ≤ 0.02) with the antifebrile efficacy determined. Together, these constituents demonstrated different pharmacokinetic properties in the febrile body.


Subject(s)
Animals , Rats , Administration, Oral , Area Under Curve , Chromatography, Liquid , Dinoprostone , Blood , Drugs, Chinese Herbal , Pharmacokinetics , Fever , Metabolism , Flavanones , Pharmacokinetics , Flavonoids , Pharmacokinetics , Glucosides , Pharmacokinetics , Interleukin-1beta , Blood , Mass Spectrometry , Monoterpenes , Pharmacokinetics , Tumor Necrosis Factor-alpha , Blood
4.
China Journal of Chinese Materia Medica ; (24): 2019-2022, 2013.
Article in Chinese | WPRIM | ID: wpr-346451

ABSTRACT

To evaluate the effects and safety of varying doses of Guizhi Fuling capsule on treating primary dysmenorrhea. From August 2010 to March 2011, 240 subjects (aged 18-30) with primary dysmenorrheal, were enrolled in 8 sites. They were randomized into Guizhi Fuling capsule high dose group, low dose group and placebo control group, 80 cases in each group. These patients were treated for three consecutive menstrual cycles, then were followed up in another three consecutive menstrual cycles. Visual analogue scales (VAS) was used to determine the pain intensity. During the treatment, the high-, low-dose and placebo groups efficiency on pain relief are 68.42%, 67.57% and 47.89% respectively. Guzhi Fuling (included high- and low- dose group) significantly relieves the pain compared to placebo. In follow-up, Guzhi Fuling groups are still superior to the placebo group (73.68%, 72.97% and 53.52%). During the treatment, pain duration reduces 57.88% in high dose group, while 46.17% in low dose group, and 30.40% in placebo group. In follow-up, pain lasting time decrease 67.93%, 53.56%, 47.46%, respectively. Guizhi Fuling significantly reduces the pain duration compared to placebo and high-dose is better than low-dose. The efficacy of Guzhi Fuling (high- and low-dose) displays certain dosage-effect relationship. Among these group, no serious adverse event was reported. Guizhi Fuling capsule at high or low dose significantly relieves the pain, improves symptoms, reduces the duration of pain, and has a better overall treatment effect and long-term treatment effect in patients with primary dysmenorrhea.


Subject(s)
Adult , Female , Humans , Capsules , Dose-Response Relationship, Drug , Double-Blind Method , Drugs, Chinese Herbal , Therapeutic Uses , Dysmenorrhea , Drug Therapy , Pain Measurement
5.
Acta Pharmaceutica Sinica ; (12): 917-924, 2013.
Article in Chinese | WPRIM | ID: wpr-259529

ABSTRACT

The current study aims to investigate the pharmacokinetic properties of Huangqin Tang on different oral doses. An LC-MS method for simultaneous determination of flavonoids and terpenoids in rat plasma was developed and validated. Plasma samples were treated with hydrochloric acid (containing 1% ascorbic acid), precipitated with acetonitrile, separated on a Zorbax SB-C18 column, detected by single quadruple mass spectrometry with an electrospray ionization interface, and quantified using selected ion monitoring mode. All pharmacokinetic parameters were processed by non-compartmental analysis using WinNonlin software. The results of specificity, linearity, intra-day and inter-day precisions, accuracy, and stability for LC-MS assay were suitable for the quantification of paeoniflorin, baicalin, wogonoside, baicalein, wogonin, oroxylin A, glycyrrhizic acid and glycyrrhetinic acid in rat plasma. The concentration-time profiles of baicalin, wogonoside, baicalein, wogonin, oroxylin A and glycyrrhizic acid showed double-peak phenomenon after Huangqin Tang was orally administered at 40 g x kg(-1) dose; all eight constituents in rat plasma showed good dose-exposure relationship within the dosage of 10-40 g x kg(-1); although plasma concentrations were different, the flavonoids with the same backbone showed the similar fate in the body with the corresponding dosage. In conclusion, the LC-MS assay was successfully applied for the pharmacokinetic study of multi-constituents of Huangqin Tang with different doses. Additionally, these constituents demonstrated good pharmacokinetic properties in the body.


Subject(s)
Animals , Male , Rats , Administration, Oral , Chromatography, Liquid , Dose-Response Relationship, Drug , Drugs, Chinese Herbal , Chemistry , Flavanones , Blood , Pharmacokinetics , Flavonoids , Blood , Pharmacokinetics , Glucosides , Blood , Pharmacokinetics , Glycyrrhetinic Acid , Blood , Pharmacokinetics , Glycyrrhizic Acid , Blood , Pharmacokinetics , Monoterpenes , Blood , Pharmacokinetics , Pentacyclic Triterpenes , Blood , Pharmacokinetics , Rats, Wistar , Spectrometry, Mass, Electrospray Ionization
6.
China Journal of Chinese Materia Medica ; (24): 59-61, 2004.
Article in Chinese | WPRIM | ID: wpr-276665

ABSTRACT

<p><b>OBJECTIVE</b>To study the effects of alum, aluminum chloride and aluminum hydroxide on aluminum contents in serum and brain of mice with high performance capillary.</p><p><b>METHOD</b>60 days after the mice were given daily alum, aluminum chloride and aluminum hydroxide with the same aluminum content of 14.25, 57 mg x kg(-1) x d(-1), respectively, the aluminum content in serum and brain of mice were determined with high performance capillary chromatography.</p><p><b>RESULT</b>The average recoveries of serum aluminum determination was 96.5%-103%. The average recoveries of brain aluminum assay was 92.2%-105.3%. Except control group, serum aluminum increased obviously. Brain aluminum increased in all the large doses groups. 2 weeks after the mice were stopped being given these drugs, serum and brain aluminum recovered to normal level, except aluminum chloride large doses group.</p><p><b>CONCLUSION</b>The metabolism and excretion mechanism of aluminum in mice depends on the chemical states of the aluminum compound.</p>


Subject(s)
Animals , Male , Mice , Administration, Oral , Alum Compounds , Pharmacokinetics , Aluminum , Blood , Metabolism , Aluminum Compounds , Pharmacokinetics , Aluminum Hydroxide , Pharmacokinetics , Brain , Metabolism , Chlorides , Pharmacokinetics , Electrophoresis, Capillary , Methods
7.
China Journal of Chinese Materia Medica ; (24): 796-818, 2004.
Article in Chinese | WPRIM | ID: wpr-272796

ABSTRACT

<p><b>OBJECTIVE</b>To study functions of Jingu Tongxiao granule (JGTXG, treatmenting ache of bones and muscles) in antiphlogistic and antalgic aspect, invigorating the circulation of blood and absorbing clots and antitraumatic soft tissue.</p><p><b>METHOD</b>Animal models of inflammation, ache, gore and traumatic soft tissue were adopted, and pharmacodynamic actions of Jingu Tongxiao granule were observed.</p><p><b>RESULT</b>JGTXG could conspicuously restrain inflammatory reactions of mouse ear tumid model treated by croton oil tumid and rat foot metatarsus tumid model treated by carrageenan, and restrain pain responses of mouse caused with whipping back end method by heat stimulating and of mouse caused with wriggling body method by acetic acid being injected in its abdominal cavity. It could significantly improve petechia degree in traumatic rat blood stasis model, and prominently improve raumatized limb's tumefaction degree and alleviate blood stasis, swelling and phlogistic cell soakage in traumatic rat soft tissue model. At the same time, it could prominently restrain platelet aggregation and improve whole blood viscosity.</p><p><b>CONCLUSION</b>Jingu Tongxiao granule has antiphlogistic and antalgic functions, invigorating the circulation of blood and absorbing clots and antitraumatic soft tissue, and it could keep curative effect of original dosage form.</p>


Subject(s)
Animals , Male , Mice , Rats , Analgesics, Non-Narcotic , Pharmacology , Anti-Inflammatory Agents, Non-Steroidal , Pharmacology , Blood Viscosity , Cinnamomum , Chemistry , Cyperus , Chemistry , Drug Combinations , Drugs, Chinese Herbal , Pharmacology , Ear Diseases , Pathology , Edema , Pathology , Hemorheology , Pain Threshold , Plants, Medicinal , Chemistry , Platelet Aggregation , Rats, Sprague-Dawley , Salvia miltiorrhiza , Chemistry
8.
China Journal of Chinese Materia Medica ; (24): 243-246, 2003.
Article in Chinese | WPRIM | ID: wpr-266776

ABSTRACT

<p><b>OBJECTIVE</b>To compare the antibacterial effects of Huangqin-Tang with its metabolites produced by intestinal flora.</p><p><b>METHOD</b>The antibacterial tests in vitro and in vivo were performed by agar dilution method and lethal protection of animal respectively.</p><p><b>RESULT</b>Huangqin-Tang and its metabolites had antibacterial action on bacteria in vitro, however the antibacterial activity of metabolites of Huangqin-Tang on Salmomella, Dysentery bacillus and Proteus in vitro was stronger than Huangqin-Tang. The metabolites of Huangqin-Tang had protective effect on the animals infected by Staphylococcus aureus and Escherichia coli respectively from death, but Huangqin-Tang had no lethal protection action.</p><p><b>CONCLUSION</b>The antibacterial effects of metabolites of Huangqin-Tang in vitro and in vivo are stronger than that of Huangqin-Tang, which shows that intestinal flora play a very important role in antibacterial effects of Huangqin-Tang.</p>


Subject(s)
Animals , Male , Mice , Anti-Bacterial Agents , Pharmacology , Therapeutic Uses , Drugs, Chinese Herbal , Pharmacology , Therapeutic Uses , Escherichia coli Infections , Drug Therapy , Feces , Microbiology , Intestines , Microbiology , Phytotherapy , Plants, Medicinal , Chemistry , Proteus , Salmonella , Shigella dysenteriae , Staphylococcal Infections , Drug Therapy
9.
China Journal of Chinese Materia Medica ; (24): 842-844, 2003.
Article in Chinese | WPRIM | ID: wpr-282230

ABSTRACT

<p><b>OBJECTIVE</b>To compare the protective activity of liver injury induced by D-galactosamine (GalN) between Huangqin-Tang and their metabolites by human intestinal bacteria(HIB).</p><p><b>METHOD</b>The liver injuries in conventional and pseudo-germfree mice were induced by GalN. After oral administration of Huangqin-Tang and their metabolites mixtures by HIB, the serum transaminase (ALT and AST) activities were detected.</p><p><b>RESULT</b>In conventional mice, large and medium doses (20 and 10 g.kg-1) of Huangqin-Tang decoction significantly reduced the increase of serum ALT activity after 18 h GalN treatment. In pseudo-germfree mice, metabolites significantly reduced the ALT levels. However, Huangqing-Tang didn't affect the ALT levels in this kind of mice. To all of the animals, AST levels remained the same after oral Huangqin-tang or their metabolites.</p><p><b>CONCLUSION</b>The metabolism by intestinal bacteria plays a role in pharmacological effects of constituents of Chinese herbal medicine. The metabolites of the constituents by intestinal bacteria were the real active components in vivo.</p>


Subject(s)
Animals , Male , Mice , Administration, Oral , Alanine Transaminase , Blood , Aspartate Aminotransferases , Blood , Bacteria , Metabolism , Chemical and Drug Induced Liver Injury , Drugs, Chinese Herbal , Metabolism , Pharmacology , Galactosamine , Intestines , Microbiology , Liver Diseases , Metabolism , Plants, Medicinal , Chemistry , Protective Agents , Metabolism , Pharmacology
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