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In this paper, the name, origin, producing area, quality evaluation, harvest and processing methods of Cyperi Rhizoma used in the famous classical formulas are researched by consulting related herbal medicines, medical books, modern documents. The results showed that although some fake products such as Cyperus stoloniferus and Scirpus plants were used as Cyperi Rhizoma, the main source in the past generations is still C. rotundus. It is recommended to use C. rotundus in the famous classical formulas. Since the Tang dynasty, Guangdong, Guangxi and Zhejiang have always been high-quality production areas of Cyperi Rhizoma. Among them, those from western Guangdong are known as Guangxiangfu, Nanxiangfu is produced in Zhejiang province. Since the modern times, the quality of Cyperi Rhizoma is best if it has a big, firm physique and strong fragrant. The common processing method is vinegar processing. It is suggested that raw materials should be used as medicine in the famous classical formulas which do not clearly indicate the processing requirements, and different processed products should be selected according to the formulas with the processing requirements.
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Objective@#To our knowledge, no definitive conclusion has been reached regarding the relationship between glucocorticoids and hypertension. Here, we aimed to explore the characteristics of glucocorticoids in participants with dysglycemia and hypertension, and to analyze their association with blood pressure indicators.@*Methods@#The participants of this study were from the Henan Rural Cohort study. A total of 1,688 patients 18-79 years of age were included in the matched case control study after application of the inclusion and exclusion criteria. Statistical methods were used to analyze the association between glucocorticoids and various indices of blood pressure, through approaches such as logistic regression analysis, trend tests, linear regression, and restricted cubic regression.@*Results@#The study population consisted of 552 patients with dysglycemia and hypertension (32.7%). The patients with co-morbidities had higher levels of serum cortisol ( @*Conclusions@#Serum deoxycortisol was positively correlated with systolic blood pressure, pulse pressure, mean arterial pressure, mean blood pressure, and mean proportional arterial pressure. Glucocorticoids (deoxycortisol and cortisol) increase the risk of hypertension in people with dysglycemia, particularly in those with T2DM.
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Adulto , Anciano , Anciano de 80 o más Años , Femenino , Humanos , Masculino , Persona de Mediana Edad , Adulto Joven , Presión Sanguínea , Estudios de Casos y Controles , China/epidemiología , Estudios de Cohortes , Glucocorticoides/sangre , Carga Glucémica , Hidrocortisona/sangre , Hipertensión/etiología , Prevalencia , Factores de Riesgo , Población RuralRESUMEN
Objective:To observe the effect of Shengyutang on the levels of monoamine neurotransmitters in the hippocampus, and explore its possible mechanism on improving the learning and memory abilities of sleep deprivation (SD) mice. Method:The 50 mice were divided into normal group, model group, estazolam group, Shengyutang low and high dose groups, with 10 mice in each group. A multi-platform water environment was used to prepare SD mouse models. The low and high-dose Shengyutang groups received intragastric administration of 12.5, 25 g·kg<sup>-1</sup>, respectively. The mice in the model group were intragastrically administered with the same dose of normal saline daily for 8 weeks. Morris water maze experiment was used to observe the behavioral changes of SD mice in the evasion latency period, the number of crossing platforms, and the stay time in the target quadrant of each group. HE staining was used to observe the pathomorphological changes of the hippocampal tissue of each group. The expression levels of eight monoamine neurotransmitters including serotonin (5-HT),dopandne (DA),epinephrine (EP),norepinephrine (NE),5-hydroxyindole acetic acid(5-HIAA), high vanillic acid (HVA), levodopa(<italic>L</italic>-DOPA),and 3,4-dihydroxyphenylacetic acid(DOPAC)were detected by high performance liquid chromatography, and the expression levels of c-Fos protein in hippocampus were detected by immunohistochemistry. Result:Compared with the normal group, the SD mice in the model group were in a poorer general state and severe fatigue was observed. Compared with the model group, SD mice in each dose group of Shengyutang got improved in eating, activity, sleep, hair color, and response to external stimuli. Compared with the normal group, the body weight of SD mice in the model group was significantly reduced (<italic>P</italic><0.05), but the body weight in the Shengyutang high-dose group increased the most as compared with the model group (<italic>P</italic><0.05). Compared with the normal group, the hippocampal cells in the model group were disorderly arranged, incomplete in shape, increased in gap and decreased in number. Compared with the model group, the number of neurons in the hippocampus of SD mice in each dose group of Shengyutang increased. Compared with the normal group, the escape latency time of SD mice in the model group was significantly prolonged, the times of crossing platform and the residence time in the target quadrant significantly decreased (<italic>P</italic><0.01). Compared with the model group, the times of crossing platform and the residence time in the target quadrant of mice in each dose group of Shengyutang significantly increased (<italic>P</italic><0.05, <italic>P</italic><0.01). Compared with the normal group, the levels of 5-HT, 5-HIAA, <italic>L</italic>-DOPA, DOPAC, EP, NE, HVA and DA in the model group significantly decreased (<italic>P</italic><0.05,<italic> P</italic><0.01); but these levels in each dose group of Shengyutang were higher than those in model group (<italic>P</italic><0.05). Compared with the normal group, the average MD value of c-Fos protein in the hippocampus of the model group significantly increased (<italic>P</italic><0.01), and the expression levels of c-Fos protein in the hippocampus of Shengyutang groups were significantly lower than those in model group (<italic>P</italic><0.01). Conclusion:Shengyutang can improve the learning and memory abilities of SD rats, and its mechanism may be related to the decrease of monoamine neurotransmitter and c-Fos protein expression.
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Malignant tumors are important diseases that threaten human health. Although targeting and immunotherapy have been gradually applied in the treatment of malignant tumors in recent years, which can alleviate the suffering of patients to a certain extent, there are still problems of large adverse reactions and easy drug resistance. At present, chemotherapy is still the main method for the treatment of malignant tumors. While killing tumor cells, chemotherapy also damages normal cells, which often leads to drug toxicity, such as bone marrow suppression, gastrointestinal adverse reactions, liver and kidney function damage, and oral mucosal reactions. Although modern medicines have a certain effect on the toxicity of chemotherapy drugs, there are still limitations. Traditional Chinese medicine(TCM) has a long history of treating malignant tumors, and considers that chemotherapy is a drug with toxin invading the body, exacerbating the "deficiency", "toxin" and "stasis" of the body, causing damage to Qi, blood and organs, especially in spleen, stomach, liver and kidney, and leading to bone marrow suppression, liver and kidney function injury and other adverse reactions. Studies have confirmed that the use of TCM treatment has a better clinical efficacy. Therefore, new therapies shall be explored based on the basic theory of traditional Chinese medicine. As the core part of the theoretical system of TCM, Viscera-state doctrine is closely related to looking, listening, questioning and feeling the pulse of TCM, and has constantly developed and improved. It has important significance in guiding diagnosis and treatment of diseases. This study is guided by viscera-state doctrine of TCM and based on the etiology and pathogenesis of TCM. It starts with the clinical manifestations of common drug toxicity of chemotherapy drugs, such as bone marrow suppression, gastrointestinal adverse reactions, liver and kidney function damage, oral mucosal reactions, which are external signs of the toxicity of chemotherapeutic drugs, and associates pathological manifestations of viscera to physiological functions. From elephants and Tibetans, it systematically summarizes the viscera characteristics of various common chemotherapeutic drugs and provides new ideas and methods for clinical use of TCM in treating the toxicity of chemotherapeutic drugs, so as to promote the application of viscera-state doctrine in diagnosis and treatment of diseases.
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Objective:To study the protective effect of Xiayuxue Tang on adenine-induced renal fibrosis model in rats and its impact on Wnt/<italic>β</italic>-catenin and transforming growth factor <italic>β</italic><sub>1</sub>(TGF-<italic>β</italic><sub>1</sub>)/Smad signal pathway. Method:A total of 50 SPF-grade male SD rats were randomly divided into 5 groups: the normal group, the model group, the losartan group (9 mg·kg<sup>-1</sup>) and low and high dose (2.43,4.86 g·kg<sup>-1</sup>) of Xiayuxue Tang groups. The rat model of renal fibrosis was established by ig administration adenine (250 mg·kg<sup>-1</sup>) for 24 consecutive days. The rats were then given the corresponding drugs for 30 consecutive days. The levels of serum creatinine(SCr) and blood urea nitrogen (BUN) were measured by enzyme-linked immunosorbent assay(ELISA). The histopathological changes of renal tissues in rats were observed by hematoxylin and eosin (HE) staining. The collagen deposition in rat renal tissue was observed by Masson staining; the protein expression levels of Wnt5a, Wnt5b, <italic>β</italic>-catenin, TGF-<italic>β</italic><sub>1</sub>, Smad4, Smad7 in renal tissue were detected respectively by immunohistochemistry(IHC) and Western blot. Result:Compared with the normal group, the results of each experimental group showed that SCr and BUN levels significantly increased in the model group (<italic>P</italic><0.01). SCr and BUN levels decreased significantly after the intervention with the Xiayuxue Tang (<italic>P</italic><0.01). Compared with the normal group, HE and Masson staining results showed that rats in the model group had severe renal interstitial damage and massive deposition of renal interstitial collagen. The renal interstitial tubule injury was relieved after the intervention with the Xiayuxue Tang, and the renal interstitial collagen deposition decreased. The results of IHC and Western blot showed that compared with the normal group, the expressions of Wnt5a, <italic>β</italic>-catenin, TGF-<italic>β</italic><sub>1</sub> protein in the kidney of rats up-regulated (<italic>P</italic><0.01), while the expressions of Wnt5b and Smad7 protein down-regulated (<italic>P</italic><0.01). After the intervention with Xiayuxue Tang, the expressions of Wnt5a, <italic>β</italic>-catenin, TGF-<italic>β</italic><sub>1</sub> protein down-regulated (<italic>P</italic><0.01), while the expressions of Wnt5b and Smad7 protein up-regulated(<italic>P</italic><0.01). There was no significant difference between the low-dose and high-dose groups with Xiayuxue Tang. Conclusion:Xiayuxue Tang has the protective effect on RIF rats induced by adenine, and its mechanism is related to the inhibition of Wnt/<italic>β</italic>-catenin and TGF-<italic>β</italic><sub>1</sub>/Smad signal pathway.
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Objective: To holistically evaluate the protective effects of water and ethanol extracts of stems and leaves of Chrysanthemum morifolium and its underlying mechanism. Methods: Gut dysfunction model was established by injection of liposaccharide in rabbits, and administrated with water and ethanol extracts of stems and leaves of C. morifolium to investigate the treatment. Feces of rabbits in each group were collected and analyzed by 1H-NMR complemented with multivariate statistical methods to evaluate the metabolic alteration. Results: Compared with the control group, the levels of lactate and formate in liposaccharide intoxicated model group were significantly increased, and the concentrations of propionate, glutamine, glutamate, aspartate were notably decreased. Both the water and ethanol extracts of stems and leaves of C. morifolium ameliorated gut dysfunction of rabbits in a similar manner, increased the decreased levels of aspartate, adenine, phenylalanine, tyrosine induced by liposaccharide, and reduced the elevated content of formate. Conclusion: Pathway analysis revealed that both the water and ethanol extracts of stems and leaves of C. morifolium could regulate the disturbed phenylalanine, tyrosine and tryptophan biosynthesis; disordered alanine, aspartate and glutamate metabolism and imbalanced glycine, serine and threonine amino acid metabolism, exerting a holistic protective effect on gut disorder. Thus, this study lays a scientific foundation for the resource utilization of stems and leaves of C. morifolium after the harvest of the inflorescence.
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The 16S rDNA sequencing method was adopted to study the effects of mulberry leaf flavonoids, polysaccharides and alkaloids on intestinal microflora in db/db diabetic mice. The animal experiment was examined by the Ethics Committee of Nanjing University of Chinese Medicine. Ten db/m mice were control group and forty db/db mice were randomly divided into model group, metformin group, mulberry flavonoid (MF) group, mulberry polysaccharide (MP) group and mulberry alkaloid (MA) group. After intragastric administration for six weeks, fresh feces were collected for detection of intestinal microflora. There were Firmicutes, Bacteroidetes, Proteobacteria, Saccharibacteria, Tenericutes, Deferribacteres, Verrucomicrobia, Cyanobacteria in each group. The results showed that the intestinal microflora of db/db mice changed significantly from phylum level to genus level. The proportion of Firmicutes and Proteobacteria in model group decreased significantly, and the proportion of Bacteroidetes increased. The difference in species abundance distribution between model group and other groups was significant, which indicated that the community distribution was disordered in model group. After administration, the Bacteroidetes, Lachnospiraceae, Roseburia and Desulfovibrio were effectively regulated, especially in the alkaloid group. The difference in species abundance distribution between drug-treated group and blank group also became smaller. It is suggested that the active components of mulberry leaf have the effect of improving the intestinal microflora imbalance in db/db mice.
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The present study is designed to explore the role of plasma cells in the change of protein C system (PCS) in ulcerative colitis (UC). Dextran sulfate sodium (DSS, 4% in concentration) was used to induce mouse UC model. The plasma cells and the type of immune complex in colon were observed by immunofluorescence. The amount and type of plasma cells separated from colonic mucosal lamina propria were detected by flow cytometry using anti-CD54CD38and IgA/M/G antibodies, respectively. After stimulation of macrophages by IgG type immune complex, TNF-α and IL-6 levels were evaluated by ELISA. After co-incubation of microvascular endothelial cells with TNF-α or IL-6, the expressions of endothelial protein C receptor (EPCR) and thrombomodulin (TM), and the activity of activated protein C (APC) were examined. As the results showed, the IgG type plasma cells infiltration and the quantity of IgG type immune complex were increased in DSS group in comparison with control group. After incubation with IgG type immune complex, the levels of TNF-α and IL-6 in the supernatant of macrophages were increased (P < 0.01) in a concentration-dependent manner. Meanwhile, after incubation with TNF-α or IL-6, the expressions of EPCR and TM in the microvascular endothelial cells were decreased (P < 0.05 or P < 0.01), while the activity of APC was reduced (P < 0.05 or P < 0.01). These results suggested that the quantity of IgG type plasma cells increases in UC and forms immune complexes, which affect the secretion of cytokines from macrophage, thereby affecting the function of endothelial cells and finally inhibiting PCS in UC. Therefore, plasma cell may be a novel target for the treatment of UC.
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The aim of this study was to investigate the regulatory effect of the total glycoside extracted from leaves of Rehmannia (TLR) and Dihuangye total glycoside capsule (DTG) on intestinal microflora in diabetic nephropathy rats. Forty-eight rats were randomly divided into the control group (C), model group (M), Huangkui capsule group (0.75 g·kg-1·d-1, HK), irbesartan group (27 mg·kg-1·d-1, YX), TLR low dose group (4.3 g·kg-1·d-1, DHYL), TLR high dose group (7.2 g·kg-1·d-1, DHYH), DTG low dose group (216 mg·kg-1·d-1, JNL), DTG high dose group (360 mg·kg-1·d-1, JNH). Rat model of diabetic nephropathy was induced by intraperitoneal injection of small dose of streptozotocin (45 mg·kg-1, STZ) and feeding high-fat diet and 5% glucose drinking water. After oral administration for two weeks, the 16S rDNA sequencing method was used to study the effects of the TLR and DTG on intestinal flora in diabetic nephropathy rats. The results showed that compared with the control group, the intestinal flora of diabetic nephropathy rats had changed from phylum units to the genus units. Moreover, the proportion of lactobacilli in the intestinal bacteria of the model group was significantly decreased, and the proportion of lactobacilli in the administration group was increased, especially the YX group, TLR low dose group and DTG low dose group. The data suggest that the total glycosides of Rehmannia glutinosa improved the disorder of intestinal flora in STZ-induced diabetic nephropathy rats.
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Hypercoagulable state and thrombosis are major lethal causes of ulcerate colitis (UC). The aim of the present study is to explore the change and role of protein C (PC) system in UC thrombosis. 4% dextran sulfate sodium (DSS) was used to induce the UC model, and the body weight, the length of colon, and the weight of spleen were measured after intake of DSS as drinking water for 1 week. The macroscore and microscore were examined. The quantity of macrophage in colon smooth muscle was observed by immunofluorescence, and TNF-α and IL-6 levels in plasma were evaluated by ELISA. Intravital microscopy was applied to observe colonic mucosal microvascular circulation, activities of PC and protein S (PS) were determined by immunoturbidimetry, endothelial cell protein C receptor (EPCR) and thrombomodulin (TM) expressions were detected by immunohistochemistry. In vitro, TNF-α and IL-6 levels were tested in supernatant of macrophage separated from colonic tissue. After stimulation of mouse colonic mucosa microvascular endothelial cells by TNF-α and IL-6 respectively, the activities of PC, PS, activated protein C (APC) were evaluated, and the expressions of EPCR and TM were detected by Western blotting. The results revealed that compared with control, the DSS mouse showed weight loss (P < 0.05), a shortened colon (P < 0.05), and swelled spleen (P < 0.05), accompanied by higher histological score (P < 0.05), as well as infiltration of macrophages, elevated TNF-α and IL-6 levels in plasma (P < 0.01). The intravital microscopy results revealed that compared with control, DSS mice showed significantly enhanced adhesion of leukocytes and colonic mucosal microvascular endothelial cells (P < 0.01), meanwhile, decreased activity of PC and PS in plasma (P < 0.01 or P < 0.05), and down-regulated expression of EPCR (P < 0.01). The degree of inflammation was negatively correlated with the PC activity. In vitro, TNF-α and IL-6 levels were increased in the supernatant of macrophages from DSS mice colonic tissue (P < 0.05), and after incubation of TNF-α or IL-6 with colonic mucosal microvascular endothelial cells, the APC activity was decreased (P < 0.05 or P < 0.01), and expression of EPCR was down regulated (P < 0.05). These results suggest that PC system is inhibited in UC mouse. Presumably, the mechanism may be due to the secretion of cytokines from macrophages and subsequential influence on the function of endothelia cells. Furthermore, enhancement of PC system activity may serve as a new strategy for the treatment of UC.
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Animales , Ratones , Factores de Coagulación Sanguínea , Metabolismo , Colitis Ulcerosa , Sulfato de Dextran , Inmunohistoquímica , Inflamación , Interleucina-6 , Sangre , Mucosa Intestinal , Patología , Macrófagos , Biología Celular , Proteína C , Metabolismo , Receptores de Superficie Celular , Metabolismo , Bazo , Patología , Factor de Necrosis Tumoral alfa , SangreRESUMEN
The study is aimed to explore the molecular mechanism of the treatment of apocynin in dextran sulfate sodium (DSS)-induced ulcerative colitis (UC) mice. 5% DSS was used to mimic the UC model, and 2% apocynin was applied to treat the UC mice. HE staining was used for histopathological evaluation. Chemiluminescence technique was used to measure reactive oxygen species (ROS) production, and the rate of consumption of NADPH inhibited by DPI was detected to determine the NADPH oxidases (NOXs) activity. Western blot was applied to identify the level of p38MAPK phosphorylation, Griess reaction assay to analyze NO production, immunoenzymatic method to determine prostaglandin E2 (PGE2) production, real time RT-PCR and Western blot to identify the expression of iNOS and COX2, and enzyme linked immunosorbent assay to detect inflammatory cytokines TNF-α, IL-6, IFN-γ, IL-1β. Rat neutrophils were separated, and then ROS production, NOXs activity, NO and PGE2 production, NOX1 and p-p38MAPK expression were detected. Compared with the UC group, apocynin decreased ROS over-production and NOXs activity (P < 0.01), reduced p38MAPK phosphorylation, inhibited NO, PGE2 and cytokines production (P < 0.01). Apocynin also decreased NOXs activity and ROS over-production (P < 0.01), inhibited p38MAPK phosphorylation and NOX1 expression, and reduced NO and PGE2 production (P < 0.01) in separated neutrophils from UC mice. Therefore, apocynin could relieve inflammation in DSS-induced UC mice through inhibiting NOXs-ROS-p38MAPK signal pathway, and neutrophils play an important role.
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Animales , Ratones , Ratas , Acetofenonas , Farmacología , Colitis Ulcerosa , Quimioterapia , Citocinas , Metabolismo , Sulfato de Dextran , Inflamación , Quimioterapia , Sistema de Señalización de MAP Quinasas , NADH NADPH Oxidorreductasas , Metabolismo , Neutrófilos , Metabolismo , Especies Reactivas de Oxígeno , Metabolismo , Proteínas Quinasas p38 Activadas por Mitógenos , MetabolismoRESUMEN
The aim of the present study was to explore the role of orphan G protein-coupled receptor 55 (GPR55) in diabetic gastroparesis (DG). Streptozotocin (STZ) was used to mimic the DG model, and the body weight and blood glucose concentration were tested 4 weeks after STZ injection (i.p.). Electrogastrogram and phenolsulfonphthalein test were used for detecting gastric emptying. Motilin (MTL), gastrin (GAS), vasoactive intestinal peptide (VIP), and somatostatin (SS) levels in plasma were determined using radioimmunology. Real-time PCR and Western blot were applied to identify the expression of GPR55 in gastric tissue, and immunohistochemistry was used to detect the distribution. The effect of lysophosphatidylinositol (LPI), an agonist of GPR55, was observed. STZ mice showed increased blood glucose concentration, lower body weight, decreased amplitude of slow wave, and delayed gastric emptying. LPI antagonized these effects of STZ. Compared to the control group, STZ caused significant decreases of MTL and GAS levels (P < 0.01), as well as increases of SS and VIP levels (P < 0.01). The changes of these hormones induced by STZ were counteracted when using LPI. GPR55 located in mice stomach, and it was up-regulated in DG. Although LPI showed no effects on the distribution and expression of GPR55 in normal mice, it could inhibit STZ-induced GPR55 up-regulation. These results suggest GPR55 is involved in the regulation of gastric movement of DG, and may serve as a new target of DG treatment. LPI, an agonist of GPR55, can protect against STZ-induced DG, and the mechanism may involve the change of GPR55 expression and modification of gastrointestinal movement regulating hormones.
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Animales , Ratones , Diabetes Mellitus Experimental , Metabolismo , Patología , Gastroparesia , Metabolismo , Patología , Lisofosfolípidos , Farmacología , Receptores de Cannabinoides , MetabolismoRESUMEN
AIM@#To study the constituents and bioactivity of Illicium simonsii.@*METHODS@#The extracts of the fruits of Illicium simonsii were submitted to a combination of chromatographic materials, silica gel, ODS column chromatography and finally preparative HPLC to obtain eight compounds which were further evaluated for their cytotoxicity by MTT method.@*RESULTS@#A new phenylpropanoid glycolside, 2, 4-dihydroxy-allylbenzene-2-O-β-D-glucopyranoside (1), together with seven characteristic sesquiterpene lactones, oligandrumin B (2), oligandrumin D (3), anisatin (4), veranisatin D (5), pseudomajucin (6), 1α-hydroxy-3-deoxy-pseudoanisatin (7), 8α-hydroxy-10-deoxycyclomerrillianolide (8) were isolated.@*CONCLUSION@#Compound 1 is new. Compounds 1, 2, 3, 5-8 were isolated from this plant for the first time. None of the isolates showed inhibitory effects on the growth of non-small cell lung tumor cell line A549.