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1.
J Tradit Chin Med ; 41(4): 530-538, 2021 08.
Article in English | MEDLINE | ID: mdl-34392645

ABSTRACT

OBJECTIVE: To investigate the anti-bacterial and anti-viral effects of Fengreqing oral liquid (, FRQ) in vitro and in vivo. METHODS: The minimum inhibitory concentrations of Fengreqing Oral Liquid against six gram-positive bacteria (Staphylococcus aureus, Streptococcus mutans, Peptostreptococcus anaerobius, Hemolytic streptococcus, Streptococcus pneumoniae, Klebsiella pneumoniae), seven gram-negative bacteria (Escherichia coli, Actinobacillus actinomycetemcomitans, Porphyromonas gingivalis, Haemophilus influenzae, Helicobacter pylori, Pseudomonas aeruginosa, Gardnerella vaginalis) and Candida albicans were detected by the paper disc diffusion method. The inhibition rate of A/PuertoRico/8/34(H1N1) (PR8) influenza virus in different concentrations of Fengreqing oral solution was detected by chicken embryo method. CCK8 method was used to detect the half-cell infection of RSV, VSV and CVB3. The effect of FRQ on the survival curve of mice was detected by using co-infection model of Streptococcus pneumoniae and influenza virus. RESULTS: In vitro, FRQ can inhibit Actinobacillus actinomycetemcomitans, Helicobacter pylori, Gardnerella vaginalis, Staphylococcus aureus, Streptococcus mutans and Streptococcus pneumoniae and has an antiviral effect on the envelope virus H1N1. In vivo, Fengreqing oral solution had therapeutic effect on influenza-Streptococcus pneumoniae co-infection in mice, significantly improving the survival rate of mice. The medium dose and low dose FRQ significantly prolonged the survival time of mice. CONCLUSION: FRQ has good anti-bacterial and anti-viral effectsin vivo and in vitro.


Subject(s)
Helicobacter pylori , Influenza A Virus, H1N1 Subtype , Animals , Anti-Bacterial Agents , Antiviral Agents , Chick Embryo , Mice , Microbial Sensitivity Tests , Staphylococcus aureus
2.
Braz J Med Biol Res ; 52(6): e8132, 2019.
Article in English | MEDLINE | ID: mdl-31141088

ABSTRACT

The aim of this study was to elucidate the concise effects of a traditional herb pair, Curcumae rhizoma-Sparganii rhizoma (CRSR), on uterine leiomyoma (UL) by analyzing transcriptional profiling. The UL rat model was made by intramuscular injection of progesterone and gavage administration of diethylstilbestrol. From 11 weeks of the establishment of the model, rats of the UL+CRSR group were gavaged daily with CRSR (6.67 g/kg). The serum concentrations of progesterone (P) and estradiol (E2) were determined by radioimmunoassay, the uterine index was measured by caliper measurement, and the pathological status was observed by hematoxylin and eosin stain. Gene expression profiling was checked by NimbleGen Rat Gene Expression Microarrays. The results indicated that the uterine mass of UL+CRSR rats was significantly shrunk and serum P and E2 levels significantly reduced compared to UL animals and nearly to the level of normal rats. Results of microarrays displayed the extensive inhibition of CRSR upon the expression of proliferation and deposition of extracellular matrix (ECM)-related genes, and significantly regulated a wide range of metabolism disorders. Furthermore, CRSR extensively regulated key pathways of the UL process, such as MAPK, PPAR, Notch, and TGF-ß/Smad. Regulation of the crucial pathways for the UL process and ECM metabolism may be the underlying mechanisms of CRSR treatment. Further studies will provide clear clues for effectively treating UL with CRSR.


Subject(s)
Curcuma/chemistry , Gene Expression Regulation, Neoplastic/drug effects , Leiomyoma/drug therapy , Plant Extracts/pharmacology , Rhizome/chemistry , Uterine Neoplasms/drug therapy , Animals , Disease Models, Animal , Female , Leiomyoma/genetics , Leiomyoma/metabolism , Oligonucleotide Array Sequence Analysis , Radioimmunoassay , Rats , Rats, Sprague-Dawley , Transcription Factors , Uterine Neoplasms/genetics , Uterine Neoplasms/metabolism
3.
Braz. j. med. biol. res ; 52(6): e8132, 2019. tab, graf
Article in English | LILACS | ID: biblio-1001537

ABSTRACT

The aim of this study was to elucidate the concise effects of a traditional herb pair, Curcumae rhizoma-Sparganii rhizoma (CRSR), on uterine leiomyoma (UL) by analyzing transcriptional profiling. The UL rat model was made by intramuscular injection of progesterone and gavage administration of diethylstilbestrol. From 11 weeks of the establishment of the model, rats of the UL+CRSR group were gavaged daily with CRSR (6.67 g/kg). The serum concentrations of progesterone (P) and estradiol (E2) were determined by radioimmunoassay, the uterine index was measured by caliper measurement, and the pathological status was observed by hematoxylin and eosin stain. Gene expression profiling was checked by NimbleGen Rat Gene Expression Microarrays. The results indicated that the uterine mass of UL+CRSR rats was significantly shrunk and serum P and E2 levels significantly reduced compared to UL animals and nearly to the level of normal rats. Results of microarrays displayed the extensive inhibition of CRSR upon the expression of proliferation and deposition of extracellular matrix (ECM)-related genes, and significantly regulated a wide range of metabolism disorders. Furthermore, CRSR extensively regulated key pathways of the UL process, such as MAPK, PPAR, Notch, and TGF-β/Smad. Regulation of the crucial pathways for the UL process and ECM metabolism may be the underlying mechanisms of CRSR treatment. Further studies will provide clear clues for effectively treating UL with CRSR.


Subject(s)
Animals , Female , Rats , Uterine Neoplasms/drug therapy , Plant Extracts/pharmacology , Gene Expression Regulation, Neoplastic/drug effects , Curcuma/chemistry , Rhizome/chemistry , Leiomyoma/drug therapy , Transcription Factors , Uterine Neoplasms/genetics , Uterine Neoplasms/metabolism , Radioimmunoassay , Rats, Sprague-Dawley , Oligonucleotide Array Sequence Analysis , Disease Models, Animal , Leiomyoma/genetics , Leiomyoma/metabolism
4.
PLoS One ; 7(9): e46574, 2012.
Article in English | MEDLINE | ID: mdl-23029551

ABSTRACT

Polydatin is one of main compounds in Polygonum cuspidatum, a plant with both medicinal and nutritional value. The possible hepatoprotective effects of polydatin on acute liver injury mice induced by carbon tetrachloride (CCl(4)) and the mechanisms involved were investigated. Intraperitoneal injection of CCl(4) (50 µl/kg) resulted in a significant increase in the levels of serum aspartate aminotransferase (AST), alanine aminotransferase (ALT) and hepatic malondialdehyde (MDA), also a marked enhancement in the expression of hepatic tumor necrosis factor-alpha (TNF-α), interleukin-1 beta (IL-1ß), cyclooxygenase-2 (COX-2), inducible nitric oxide synthase (iNOS) and nuclearfactor-kappa B (NF-κB). On the other hand, decreased glutathione (GSH) content and activities of glutathione transferase (GST), superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPx) were observed following CCl(4) exposure. Nevertheless, all of these phenotypes were evidently reversed by preadministration of polydatin for 5 continuous days. The mRNA and protein expression levels of hepatic growth factor-beta1 (TGF-ß(1)) were enhanced further by polydatin. These results suggest that polydatin protects mice against CCl(4)-induced liver injury through antioxidant stress and antiinflammatory effects. Polydatin may be an effective hepatoprotective agent and a promising candidate for the treatment of oxidative stress- and inflammation-related diseases.


Subject(s)
Anti-Inflammatory Agents/pharmacology , Antioxidants/pharmacology , Chemical and Drug Induced Liver Injury/drug therapy , Drugs, Chinese Herbal/pharmacology , Fallopia japonica/chemistry , Glucosides/pharmacology , Stilbenes/pharmacology , Alanine Transaminase/blood , Animals , Anti-Inflammatory Agents/therapeutic use , Antioxidants/therapeutic use , Aspartate Aminotransferases/blood , Carbon Tetrachloride , Catalase/metabolism , Chemical and Drug Induced Liver Injury/blood , Chemical and Drug Induced Liver Injury/pathology , Drugs, Chinese Herbal/therapeutic use , Gene Expression , Glucosides/therapeutic use , Glutathione/metabolism , Glutathione Peroxidase/metabolism , Glutathione Transferase/metabolism , Inflammation Mediators/metabolism , Liver/drug effects , Liver/enzymology , Liver/metabolism , Male , Mice , Mice, Inbred ICR , NF-kappa B/metabolism , Oxidative Stress/drug effects , Stilbenes/therapeutic use , Superoxide Dismutase/metabolism , Transforming Growth Factor beta1/genetics , Transforming Growth Factor beta1/metabolism , Up-Regulation
5.
J Ethnopharmacol ; 144(3): 791-6, 2012 Dec 18.
Article in English | MEDLINE | ID: mdl-23085396

ABSTRACT

ETHNOPHARMACOLOGICAL RELEVANCE: Ligusticum chuanxiong Hort. (Umbelliferae) is a plant used as medicine and food in China. The essential oil (EO) extracted from its rhizomes possesses many pharmacological activities. However, there have been no scientific reports in the modern literature on the safety of EO. AIMS OF THE STUDY: The objective of this study was to conduct a chemical composition analysis and evaluate acute toxicity and skin sensitivity of EO from rhizomes of Ligusticum chuanxiong. MATERIALS AND METHODS: The chemical composition of hydrodistilled EO was analyzed by gas chromatography-mass spectrometry (GC-MS) and was evaluated in animals for acute toxicity, skin irritation and sensitization tests. RESULTS: Dozens of compounds were detected and the major components of EO were ligustilide and butylidenephthalide with relative contents of 67.46 and 5.06%, respectively. The oral and intra-peritoneal lethal doses of 50% (LD(50)) in mice were 7.23 g/kg (approximately 14,606 times of clinical dose used) and 2.25 g/kg (approximately 5091 times of clinical dose used), respectively. The doses of 0.115 and 0.23 g/kg EO (approximately 232.5 and 465 times of the respective clinical doses used) revealed slight irritation effects on rabbit skin, but 1g/kg EO (approximately 2020 times of clinical dose used) had no observable effect on guinea pig skin in the skin sensitization test. CONCLUSIONS: These experimental results indicate that short term application of EO is probably safe within the range of its clinical doses, but the dose should be controlled for external use due to its slight skin irritation.


Subject(s)
Irritants/toxicity , Ligusticum , Oils, Volatile/toxicity , 4-Butyrolactone/analogs & derivatives , 4-Butyrolactone/analysis , 4-Butyrolactone/toxicity , Animals , Female , Guinea Pigs , Irritants/chemistry , Male , Mice , Mice, Inbred ICR , Oils, Volatile/chemistry , Rabbits , Rhizome/chemistry , Skin/drug effects , Toxicity Tests, Acute
6.
J Ethnopharmacol ; 139(1): 149-54, 2012 Jan 06.
Article in English | MEDLINE | ID: mdl-22075456

ABSTRACT

ETHNOPHARMACOLOGICAL RELEVANCE: Cynoglossum lanceolatum Forsk. (Boraginaceae) has been used in folk medicine in china to treat acute nephritis, periodontitis, acute submandibular lymphadenitis, snake bite, etc. However, there have been no scientific reports in the modern literature on the diuretic, anti-inflammatory and analgesic effects of this plant. The objective of this study is to evaluate the above activities of the Cynoglossum lanceolatum extract (CLE) in animals. MATERIALS AND METHODS: The diuretic effect of CLE was assessed in rats and rabbits. The anti-inflammatory activity was evaluated using fresh egg white-induced paw edema in rats, carrageenan-elicited paw edema in adrenalectomized rats, and dimethylbenzene-induced inflammation in mice. The analgesic action was estimated in mice using the acetic acid-induced writhing test and the hot-plate test. In addition, the acute oral toxicity of CLE was studied in mice. RESULTS: CLE strikingly and dose-dependently increased urine output of rats and rabbits, suppressed fresh egg white-induced paw edema in rats and carrageenan-elicited paw edema in adrenalectomized rats, reduced dimethylbenzene-induced ear edema in mice, inhibited the writhing response in mice, but did not increased reaction time of mice in the hot-plate test. No death of mice was observed when orally administered CLE up to 12g/kg. CONCLUSIONS: These findings propose that CLE has evident diuretic, anti-inflammatory, and non-central analgesic activities. Furthermore the anti-inflammatory action does not rely on endogenetic glucocorticoids regulated by hypothalamo-pituitary-adrenal axis. On the other hand, CLE also shows a favorable safety.


Subject(s)
Analgesics/therapeutic use , Anti-Inflammatory Agents/therapeutic use , Boraginaceae , Diuretics/pharmacology , Inflammation/drug therapy , Pain/drug therapy , Acetic Acid , Animals , Carrageenan , Disease Models, Animal , Drugs, Chinese Herbal/therapeutic use , Ethanol/chemistry , Female , Inflammation/chemically induced , Inflammation/pathology , Male , Mice , Ovalbumin , Pain/chemically induced , Pain/physiopathology , Phytotherapy , Plant Roots , Rabbits , Rats , Rats, Sprague-Dawley , Sodium Chloride/pharmacology , Solvents/chemistry , Urination/drug effects , Xylenes
7.
Pharm Biol ; 49(4): 403-7, 2011 Apr.
Article in English | MEDLINE | ID: mdl-21428865

ABSTRACT

CONTEXT: In folk medicine in China, Desmodium caudatum (Thunb.) DC (Leguminosae) has been used to treat febrile diseases, rheumatic arthritis, and bacillary dysentery; nevertheless, there have been no reports on the analgesic, antipyretic, and anti-inflammatory effects of this plant in animals. OBJECTIVE: To investigate the analgesic, anti-inflammatory, and antipyretic activities of D. caudatum extract (DCE) in animals. MATERIALS AND METHODS: The analgesic effect of DCE was measured in mice using the acetic acid-induced writhing test and the hot-plate test. The anti-inflammatory activity was assessed using the carrageenan-induced rat paw edema model and the dimethylbenzene-induced mouse inflammation model. The antipyretic effect was estimated using the lipopolysaccharide (LPS)-induced rat fever model. In addition, the acute oral toxicity of DCE was studied. RESULTS: DCE significantly and dose-dependently inhibited the writhing responses in mice, increased reaction time in mice in the hot-plate test, reduced carrageenan-induced paw edema in rats and the dimethylbenzene-induced ear edema in mice, and attenuated LPS-induced fever in rats. Furthermore, no death was observed when mice were orally administered DCE up to 40 g/kg. DISCUSSION AND CONCLUSION: DCE possesses evident analgesic, anti-inflammatory, and antipyretic activities, and has a favorable safety, which supports the use of D. caudatum as an analgesic, anti-inflammatory and antipyretic drug in folk medicine.


Subject(s)
Analgesics/pharmacology , Anti-Inflammatory Agents/pharmacology , Antipyretics/pharmacology , Fabaceae , Phytotherapy , Plant Extracts/pharmacology , Analgesia , Analgesics/toxicity , Animals , Anti-Inflammatory Agents/toxicity , Antipyretics/toxicity , China , Drugs, Chinese Herbal/pharmacology , Edema/chemically induced , Edema/drug therapy , Fever/drug therapy , Inflammation/drug therapy , Male , Mice , Mice, Inbred ICR , Pain Measurement/drug effects , Plant Extracts/toxicity , Plants , Rats , Rats, Sprague-Dawley , Rats, Wistar
8.
Phytomedicine ; 15(8): 587-94, 2008 Aug.
Article in English | MEDLINE | ID: mdl-18289838

ABSTRACT

Although normal cognitive changes take place when a person becomes older, aging in humans is generally associated with deterioration of cognitive performance and, in particular, of learning and memory. These cognitive deficits can cause debilitating consequences due to aging. There are a number of herbal medicines which are reported to improve brain function including intelligence. In the present study, improving effects of tenuifolin, extracted from Radix Polygalae (RP), on learning and memory in aged and dysmnesia mice were determined using step-down type passive avoidance test or Y type maze trial. Oral administration of tenuifolin (0.02, 0.04, 0.08 g/kgd(-1), for 15 d) evidently improved the latency and number of errors in aged and dysmnesia mice. The levels of cortical acetylcholine esterase (AChE) activity and hippocampal neurotransmitters in aged mice given tenuifolin (0.02, 0.04, 0.08 g/kgd(-1), for 15 d) were also investigated, and increased levels of norepinephrine (NE), dopamine (DA), decreased activity of AChE were found. However, serotonin (5-HT) had no significant difference from that of aged mice given distilled water. The evident improvement of learning and memory of aged mice is carried out by the effects of tenuifolin on the three stages of memory process, that is, acquisition, consolidation and retrieval. This may do so by relatively increasing the levels of NE, DA in the hippocampus and by decreasing the activity of AChE in the cortex.


Subject(s)
Behavior, Animal/drug effects , Diterpenes, Kaurane/chemistry , Diterpenes, Kaurane/pharmacology , Learning/drug effects , Memory/drug effects , Plant Roots/chemistry , Polygala/chemistry , Acetylcholinesterase/metabolism , Aging/physiology , Amnesia/drug therapy , Animals , Dopamine/metabolism , Dose-Response Relationship, Drug , Male , Mice , Norepinephrine/metabolism , Phytotherapy , Serotonin/metabolism , Triterpenes/chemistry
9.
J Pharm Pharmacol ; 59(2): 301-9, 2007 Feb.
Article in English | MEDLINE | ID: mdl-17270083

ABSTRACT

Although there are normal cognitive changes that take place as a person becomes older, ageing in humans is generally associated with a deterioration of cognitive performance, in particular of learning and memory. There are a number of herbal medicines that are reported to improve brain function and intelligence. In the present study, the ameliorating effects of an essential oil extracted from Acori graminei rhizoma on learning and memory in aged, dysmnesia rats and mice were determined using the step-down passive avoidance test and Y maze. Oral administration of the essential oil (0.02, 0.04 and 0.08 g kg(-1)) to rats for 30 days and to mice for 15 days improved the latency and number of errors in aged, dysmnesia rats and mice. The cerebral neurotransmitters in aged rats given the essential oil (0.02, 0.04, 0.08 g kg(-1)) for 30 days were also investigated, and increased levels of norepinephrine, dopamine and serotonin, and decreased levels of acetylcholinesterase activity were found. The results suggest that the essential oil improves cognitive function in aged animals possibly by increasing norepinephrine, dopamine and serotonin relative levels, and by decreasing the activity of acetylcholinesterase in the cerebra.


Subject(s)
Drugs, Chinese Herbal/chemistry , Learning/drug effects , Memory/drug effects , Oils, Volatile/pharmacology , Acetylcholinesterase/metabolism , Age Factors , Animals , Cognition Disorders/chemically induced , Cognition Disorders/drug therapy , Dopamine/metabolism , Ethanol , Maze Learning/drug effects , Mice , Neurotransmitter Agents/metabolism , Nitrates , Norepinephrine/metabolism , Oils, Volatile/isolation & purification , Oils, Volatile/therapeutic use , Rats , Scopolamine , Serotonin/metabolism , Telencephalon/drug effects , Telencephalon/metabolism
10.
Zhongguo Zhong Yao Za Zhi ; 32(20): 2118-23, 2007 Oct.
Article in Chinese | MEDLINE | ID: mdl-18306741

ABSTRACT

OBJECTIVE: To investigate the correlation between decocting time (DT), administration dosage (AD) and efficacy of warming Yang of crude lateral root of aconite (CLRA) , and the best DT and AD to efficacy of warming Yang of the CLRA. METHOD: According to the efficacy of the CLRA supplementing fire and strengthening Yang, several animal models, including a constipation induced by insufficiency of Yang, kidney Yang deficient models, uniform design (UD) and regression analysis were applied to confirm the best DT and AD of the different actions of the CLRA. RESULT: The CLRA obviously improved the general state of kidney-yang deficiency mice, markedly increased their swimming depleted time in lower temperature, and evidently decreased the defecation latency, promoted defecation amount, and improved peristalsis frequency of intestines and stomach. The best DT and AD were 6 hours and 12 g x kg(-1) respectively for the CLRA to warm the kidney, spleen yang and to smooth defecation. CONCLUSION: The CLRA possesses the remarkable efficacy of warming Yang, which is obviously correlated with the DT and AD. The best DT and AD for CLRA to warm Yang are 6 hours and 12 g x kg(-1) respectively.


Subject(s)
Aconitum/chemistry , Drugs, Chinese Herbal/pharmacology , Kidney Diseases/drug therapy , Yang Deficiency/drug therapy , Animals , Body Temperature/drug effects , Constipation/drug therapy , Dose-Response Relationship, Drug , Drugs, Chinese Herbal/administration & dosage , Drugs, Chinese Herbal/isolation & purification , Drugs, Chinese Herbal/therapeutic use , Female , Gastrointestinal Motility/drug effects , Kidney Diseases/physiopathology , Male , Mice , Phytotherapy , Plant Roots/chemistry , Plants, Medicinal/chemistry , Random Allocation , Rats , Rats, Sprague-Dawley , Time Factors , Yang Deficiency/physiopathology
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