Qualitative and quantitative analysis of chemical compounds in 3 species of wild Veratrum from Inner Mongolia / 中国药房

OBJECTIVE To conduc t qualitative and quantitative analysis for the chemical compounds in 3 species of wild Veratrum（V. nigrum ，V. maackii ，V. dahuricum ）from Inner Mongolia. METHODS HPLC-Q-Exactive-MS/MS technology was used to identify the chemical components of V. nigrum ，V. maackii and V. dahuricum by consulting SciFinder ，ChemSpider database and related literatures and comparing with the reference substance. The contents of polydatin ，oxyresveratrol and resveratrol in 3 species of wild Veratrum were determined by HPLC. RESULTS A total of 31 compounds were identified ，including 13 stilbenes， 11 flavonoids，4 organic acids ，2 glycosides，1 brasilin. Most of the compounds were shared by 2 or 3 species of wild Veratrum， only 2 flavonoids kaempferol and luteolin were owned by V. dahuricum . The total contents of polydatin ，oxyresveratrol and resveratrol in 3 species of wild Veratrum were in the range of 6.618-11.292 mg/g，and the total contents of them in V. nigrum were the highest ，followed by V. maackii and V. dahuricum . The contents of polydatin and resveratrol in V. maackii were the highest ，and the content of oxyresveratrol in V. nigrum was highest. CONCLUSIONS Most of the components of 3 species of wild Veratrum are similar，only kaempferol and luteolin are unique to V. dahuricum . The contents of polydatin ，oxyresveratrol and resveratrol are significantly different among 3 species of wild Veratrum.

Advances in studies on steroidal alkaloids and their pharmacological activities in genus Veratrum / 中国中药杂志

Genus Veratrum plants contain a diversity of steroidal alkaloids, so far at least 184 steroidal alkaloids attributed to cevanine type(A-1～A-69), veratramine type(B-1～B-21), jervanine type(C-1～C-31), solanidine type(D-1～D-10) and verazine type(E-1～E-53), respectively, have been isolated and identified in the genus Veratrum. Their pharmacological activities mainly focused on decreasing blood pressure, anti-platelet aggregation and anti-thrombosis, anti-inflammatory and analgesic, and antitumor effect. This paper classified and summarized the 184 kind of steroidal alkaloids from the Veratrum plants and their major pharmalogical activities in order to provide the scientific basis for the further development and utilization of active alkaloids.

A new alkaloid from Veratrum grandiflorum / 中草药

Objective: To study the chemical constituents of the roots and rhizomes of Veratrum grandiflorum and its antitumor activities. Methods: The compounds were isolated and purified by silica gel, C-18 reversed phase column chromatography, and their structures were identified by MS and NMR analyses. The cytotoxic activities of compounds 1-6 against HepG2 (human liver cancer cell line) were evaluated by MTT method. The effect of compound 3 on cell apoptosis of HepG2 was detected by flow cytometry. Results: Eight steroidal alkaloids were isolated and their structures were identified as (3S,15S)-3β-angeloyl-15α-acetylzygadenine (1), epirubijervine (2), veratramine (3), jervine (4), 3-angeloylzygadenine (5), veratrosine (6), veramitaline (7) and veralkamine (8). Conclusion: Compound 1 is a new alkaloid, compounds 7-8 are isolated from this plant for the first time. Compound 3 showed moderate cytotoxic activity against human tumor cell line HepG2 with IC50 value of (13.70 ± 0.99) μmol/L, and induced early apoptosis of HepG2 cells.

Effect of pterostilbene on the expression and activity of antioxidant enzymes in ultraviolet B-radiated HaCaT Cells / 中华皮肤科杂志

Objective To evaluate the protective effect of pterostilbene against ultraviolet B (UVB)-induced acute damage in HaCaT cells,and to explore related mechanisms.Methods The 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazo1ium (MTS) assay and flow cytometry were performed to estimate the proliferative activity and the apoptosis and necrosis rate of HaCaT cells treated with different concentrations of pterostilbene respectively,so as to screen the non-toxic concentration of pterostilbene.HaCaT cells were randomly divided into several groups:normal control group receiving no treatment,UVB group irradiated with 57 mJ/cm2 UVB,3 pterostilbene groups treated with 2.44,4.88 and 9.75 μmol/L pterostilbene respectively for 24 hours,3 pterostilbene + UVB groups treated with 2.44,4.88 and 9.75 μmol/L pterostilbene respectively for 24 hours followed by UVB radiation.Western blot analysis was conducted to detect changes of the transcription factor NF-E2-related factor 2 (Nrf2) expression in cell nuclei and cytoplasm before and after the treatment with pterostilbene and UVB,quantitative PCR to determine the mRNA expression of catalase and superoxide dismutase in the HaCaT cells,and enzyme-linked immunosorbent assay (ELISA) to evaluate the activity of catalase and superoxide dismutase.Results MTS assay and flow cytometry showed that 2.44,4.88 and 9.75 μmol/L pterostilbene had non-toxic effect on HaCaT cells.The protein expression of Nrf2 in the nuclei and cytoplasm in the normal control group was 1.03 ± 0.08 and 1.04 ± 0.11 respectively.Compared with the normal control group,the protein expression of Nrf2 in the nuclei and cytoplasm experienced no significant changes in the 2.44-,4.88-and 9.75-μmol/L pterostilbene groups,and the UVB group showed similar protein expression of Nrf2 in the cytoplasm,but significantly increased protein expression of Nrf2 in the nuclei (1.77 ± 0.08,q =17.24,P ＜ 0.01).Compared with the normal control group and UVB group,the 2.44-,4.88-and 9.75-μmol/L pterostilbene + UVB groups all showed significantly lower protein expression of Nrf2 in the cytoplasm (0.86 ± 0.10,0.87 ± 0.11 and 0.46 ± 0.11 respectively,all P ＜ 0.05),but significantly higher protein expression of Nrf2 in the nuclei (2.38 ± 0.11,2.57 ± 0.11 and 2.07 ± 0.13,all P ＜ 0.01).As qPCR showed,UVB radiation could significantly inhibit the mRNA expression of CAT (P ＜ 0.05),but had no obvious effect on the mRNA expression of SOD (P ＞ 0.05).The mRNA expression of CAT and SOD experienced no significant changes in the 2.44-,4.88-and 9.75-μmol/L pterostilbene groups compared with the normal control group (P ＞ 0.05).However,2.44,4.88 and 9.75 μmol/L pterostilbene could significantly reduce the inhibitory effect of UVB radiation on the mRNA expression of CAT (P ＜ 0.05) and up-regulate the mRNA expression of SOD in the pterostilbene + UVB groups (P ＜ 0.05).ELISA revealed that UVB radiation could inhibit the activity of CAT and SOD in the HaCaT cells (both P ＜ 0.001),while 2.44,4.88 and 9.75 μmol/L pterostilbene could reduce the inhibitory effect of UVB radiation on the activity of CAT and SOD (all P ＜ 0.05).However,the activity of CAT and SOD were still lower in the 2.44-,4.88-and 9.75-μmol/L pterostilbene + UVB groups than in the normal control group (P ＜ 0.05).Conclusion Pterostilbene can prevent UVB-induced acute damage in HaCaT cells by activating the Nrf2 pathway and up-regulating the expression of the downstream antioxidant enzymes CAT and SOD.

Effects of resveratrol on motor function and anterior horn neuron of spinal cord following acute sciatic nerve compression injury in rats / 中国医师杂志

Objective To investigate the effects of resveratrol (Res) on motor function and the anterior horn neuron of lumbar spinal cord after acute sciatic nerve compression injury in rats.Methods The rat model with acute sciatic nerve compression injury was established in 32 Sprague Dawley (SD) rats,which were randomly divided into four groups:Res group,Dimethyl Sulfoxide (DMSO) group,Normal Saline (NS) group and sham-operation group.Res,DMSO and saline were successively injected by intraperitoneal for 10 days after established crush acute sciatic nerve compression injury model,while sham-operation group was sutured only after exposure to the sciatic nerve.The weight,the change of toe extension angle,and the sciatic functional index (SFI) of rats were observed at the 1st day before operation and the 1st,3rd,7th,and 10th days after surgery.The expressions of neuron-specific nuclear protein (NeuN) and microtubule-associate protein 2 (MAP2) were detected by immunofluorescent staining of I4-L6 spinal cord anterior horn on the 10th day after surgery.Results No significant changes were found in the weight of rats among four groups.Compared to the sham,the motor function of the injured limb in Res,DMSO,and NS rats was impaired,and the anterior horn neurons were seriously damaged.But the differences of the change of toe extension and the sciatic functional index of rats were significantly higher in Res group than that of the DMSO group and NS group (P ＜ 0.01) at the 3rd,7th,and 10th days after surgery.The expressions of NeuN and MAP2 in the anterior horn of rat lumbar spinal cord were up-regulated in Res group relative to DMSO and NS,and the number of neurons in the lumbar spinal cord was significantly relieved at the 10th days.Conclusions Res was significant to rat model of acute sciatic nerve injury,which could increase the number of neurons in the anterior horn of the spinal cord and help the recovery of motor function.

Effects of resveratrol on motor function and anterior horn neuron of spinal cord following acute sciatic nerve compression injury in rats / 中国医师杂志

Objective To investigate the effects of resveratrol (Res) on motor function and the anterior horn neuron of lumbar spinal cord after acute sciatic nerve compression injury in rats.Methods The rat model with acute sciatic nerve compression injury was established in 32 Sprague Dawley (SD) rats,which were randomly divided into four groups:Res group,Dimethyl Sulfoxide (DMSO) group,Normal Saline (NS) group and sham-operation group.Res,DMSO and saline were successively injected by intraperitoneal for 10 days after established crush acute sciatic nerve compression injury model,while sham-operation group was sutured only after exposure to the sciatic nerve.The weight,the change of toe extension angle,and the sciatic functional index (SFI) of rats were observed at the 1st day before operation and the 1st,3rd,7th,and 10th days after surgery.The expressions of neuron-specific nuclear protein (NeuN) and microtubule-associate protein 2 (MAP2) were detected by immunofluorescent staining of I4-L6 spinal cord anterior horn on the 10th day after surgery.Results No significant changes were found in the weight of rats among four groups.Compared to the sham,the motor function of the injured limb in Res,DMSO,and NS rats was impaired,and the anterior horn neurons were seriously damaged.But the differences of the change of toe extension and the sciatic functional index of rats were significantly higher in Res group than that of the DMSO group and NS group (P ＜ 0.01) at the 3rd,7th,and 10th days after surgery.The expressions of NeuN and MAP2 in the anterior horn of rat lumbar spinal cord were up-regulated in Res group relative to DMSO and NS,and the number of neurons in the lumbar spinal cord was significantly relieved at the 10th days.Conclusions Res was significant to rat model of acute sciatic nerve injury,which could increase the number of neurons in the anterior horn of the spinal cord and help the recovery of motor function.

A Patient Presenting with Elevations of Cardiac Enzyme Levels after Veratrum Oxysepalum Ingestion

Veratrum patulum has toxicological relevance because of the potential for misidentification of this plant as mountain garlic. Veratrum patulum has an ester-alkaloid that provokes cardiac arrhythmias by excessive vagal stimulation and depression of the sinoatrial and atrioventricular nodes of the heart and hypotension, cardiomegaly. We report on a retrospective case of successful outcome in patients with veratrum patulum poisoning through active treatment from the early phase after ingestion. We report on a case involving a patient who experienced dizziness, dyspnea, hypotension, and elevation of cardiac enzyme, cardiomegaly. These cases were kept under observation and generally recovered with supportive care. We report on cases of veratrum patulum poisoning with review of literature.

Influence of resveratrol on blood lipid level and ADRP expression in atherosclerosis model rabbits / 心血管康复医学杂志

Objective:To explore the influence of resveratrol on blood lipid level and expression of adipose differenti-ation related protein (ADRP)in atherosclerosis (AS)model rabbits.Methods:A total of 36 New Zealand rabbits were randomly and equally divided into normal control group,AS model group,low dose resveratrol group (low dose group)and high dose resveratrol group (high dose group).Rabbits received 15-week administration,expression level of serum lipoprotein,ADRP and ADRPmRNA expressions in adipocytes of rabbit aortic tissue were measured and compared among all groups before and after treatment.Results:Compared with AS model group at the end of 15th week,there were significant reductions in serum concentrations of total cholesterol [TC,(18.25±4.35)mmol/L vs.(12.79±2.45)mmol/L,(10.35±2.80)mmol/L],triglyceride [TG, (3.15±0.94)mmol/L vs. (2.63± 0.75)mmol/L、(1.18±0.64)mmol/L]and low density lipoprotein cholesterol [LDL-C,(15.18±3.65)mmol/L vs.(8.35±1.15)mmol/L,(7.18±1.75)mmol/L],and significant rise in level of high density lipoprotein choles-terol [HDL-C,(1.02±0.36)mmol/L vs.(3.22±1.02)mmol/L,(2.72±0.82)mmol/L]in low dose group and high dose group (P <0.05 or <0.01),and significant reduction in level of triglyceride [TG,(3.15±0.94)mmol/L vs.(1.18±0.64)mmol/L]in high dose group,P <0.01;ADRP histochemical staining [(0.43±0.05)vs.(0.35± 0.04),(0.38±0.15)]and ADRPmRNA expression [(2.47±0.94)vs.(1.30±0.49),(1.83±0.61)]significantly weakened in adipocytes of aortic tissue in low dose group and high dose group,P <0.01 all. Conclusion:Resveratrol can inhibit the overexpression of ADRP and its mRNA in adipocytes of aortic tissue in AS rabbits,reduce blood lipid levels,and help to delay the AS progression.

In vitro assessment of increasing cytotoxicity of Veratrum nigrum induced by Panax ginseng / 军事医学

Objective To compare the potential cytotoxicity induced by Veratrum nigrum coadministered with Panax ginseng, and to provide experimental evidence on the mode of herb-herb interaction based on human liver drug metabolizing enzymes.Methods The effect of V.nigrum and coadministration on cultured human hepatoma (HepG2) cells was investi-gated by detecting morphological changes , cell viability , cytomembrane integrity and apoptosis after the cells were treated for 24 h.The mRNA expression levels of drug metabolizing enzymes influenced by P.ginseng were determined by real-time quantitative reverse-transcriptase polymerase chain reaction .Results V.nigrum coadministered with P.ginseng had a better inhibitive effect on the growth of HepG2 cells at the IC50value of (15.18 ±1.03) mg/ml than at the value of IC50 (21.46 ±1.10) mg/ml of V.nigrum.Coadministration more significantly raised the LDH level in cell culture medium than at the same dose of V.nigrum.Moreover, in coadministration group, compared with the same dose of V.nigrum,the total apoptosis and necrosis of HepG2 cells were significantly increased .P.ginseng had effect on the expression of CYP3A4, CYP1A1, CYP1A2, CYP2B6 and CYP2E1 mRNA.Conclution Compatibility of medicines in a prescription also has herb-herb interactions based on drug metabolizing enzymes .The interaction mode is that the P.ginseng inhibits and induces CYPs and the modulated CYP isozymes ,inturn,have an impact on the metabolism of constituens in coadministered herbs causing herb-herb interaction .

Effect on Liver and Kidney of Mice by Traditional Chinese Medicine Compatibility of Paeoniae Radix Rubra and Veratrum Nigrum / 中国中医药信息杂志

Objective To investigate the damage of mice liver and kidney with the compatibility application of Paeoniae radix rubra and Veratrum nigrum, and explore its mechanism. Methods We examined the alanine aminotransferase, aspartate aminotransferase (AST), lactic dehydrogenase, creatinine and urea nitrogen from serum, and glutathion peroxidase (GSH-Px) and malondialdehyde (MDA) from liver and kidney tissue after intragastric administration of different ratio (4∶1, 2∶1, 1∶1, 1∶2, 1∶4) of Paeoniae radix rubra and Veratrum nigrum in mice for 22 d. Results Paeoniae radix rubra used with Veratrum nigrum did not induce the obvious damage to liver with AST increase, but induced the obvious damage to kidney. At the same time, the depressed GSH-Px activity and the increased MDA content were observed in kidney tissue. When Paeoniae radix rubra and Veratrum nigrum is on a ratio of 2∶1, the kidney injury was the most obvious. Conclusion Paeoniae radix rubra used with Veratrum nigrum in varying proportions could induce the kidney injury in mice which is related to the oxidation-antioxidation balance disturbance.

Effects of propofol combined with resveratrol pretreatment on hepatic ischemia-reperfusion injury in rats / 中华麻醉学杂志

Objective To evaluate the effects of propofol combined with resveratrol on hepatic ischemiareperfusion (I/R) injury in rats.Methods One hundred and eight male Sprague-Dawley rats,aged 6-7 weeks,weighing 220-270 g,were randomly divided into 6 groups (n =18 each):sham operation group (group S) ; I/R group; solvent group (group TW-80) ; propofol group (group P) ; resveratrol group (group R) ; propofol combined with resveratrol group (group P + R).The animals were anesthetized with intraperitoneal 10 ％ chloral hydrate 3.5-4.0 ml/kg.Liver ischemia was produced by clamping the first hepatic portal for 30 min,followed by 12 h reperfusion.In group P,propofol was infused intravenously at 10 mg· kg-1 ·h-1 starting from 10 min before ischemia until the end of operation.In group R,resveratrol 10 mg/kg was injected intravenously at 10 min before ischemia.In group P + R,resveratrol 10 mg/kg was injected intravenously and then propofol was infused intravenously at 10 mg· kg-1· h-1 starting from 10 min before ischemia until the end of operation.The equal volume of normal saline was given instead in groups S and I/R,and the equal volume of TW-80 was given instead in group TW-80.Six rats in each group were chosen at 3,6 and 12 h of reperfusion and blood samples were taken from the superior and inferior vena cava for measurement of serum alanine aminotransferase (ALT) and aspartate amino transferase (AST) activities.The rats were then sacrificed and livers were removed for microscopic examination and for determination of superoxide dismutase (SOD) and myeloperoxidase (MPO) activities,inducible nitric oxide synthase (iNOS) expression,and malondialdehyde (MDA) and nitric oxide (NO) contents in liver tissues.Results Compared with group S,the serum ALT and AST activities,and MDA and NO contents,MPO activity and iNOS expression in liver tissues were significantly increased,and the activities of SOD were decreased in the other four groups (P ＜0.05).Compared with group I/R,the serum ALT and AST activities,and MDA and NO contents,MPO activity and iNOS expression in liver tissues were significantly decreased,and the activities of SOD were increased in groups P,R and P + R (P ＜ 0.05).Compared with groups P and R,SOD activity was significantly increased,and the other parameters were decreased in group P + R (P ＜ 0.05).The pathological changes were significantly attenuated in groups P,R and P + R compared with group I/R.Conclusion Pretreatment with propofol and resveratrol can attenuate hepatic I/R injury in rats by increasing antioxidation and inhibiting lipid peroxidation and reducing production of endogenous NO,and the combination of the two agents provides better efficacy than etheir alone.

Two Cases of Poisoning with Veratrum Maackii

Veratrum alkaloids in Veratrum maackii may cause significant gastrointestinal symptoms, bradycardia, hypotension, and arrythmia. We experienced successful outcomes in two patients who were victims of poisoning due to ingestion of Veratrum maackii, which was mistaken for Allium victorialis var. platyphyllum. One patient developed hypotension and prolongation of QT interval in electronicardiogram (ECG) and was treated with administration of vasopressor and magnesium. The other patient developed bradycardia and was treated with administration of atropine. Both patients were kept under close observation, and received supportive care, and both patients were discharged without any symptoms or complications.

UHPLC-Q-TOF/MS in rapid separation and identification of chemical components in Veratrum nigrum L / 第二军医大学学报

Objective To identify the chemical components in traditional Chinese herbal medicine Veratrum nigrum L. using ultra-performance liquid chromatography/electrospray ionization quadrupole time-of-flight tandem mass spectrometry (UHPLC-Q-TOF/MS). Methods An Agilent Eclipse Plus C18 (2. 1 mm × 100 mm, 1. 8 μm) was used for isolation and identification of the chemical components in Veratrum nigrum L., with a mobile phase using 0. 1% formic acid aqueous solvent (A) and ACN (B) for gradient elution. The data were collected by the positive ion mode using ESI ion source. Results Thirty-two chemical compounds were identified from Veratrum nigrum L. The chemical structures of three pairs of steroidal alkaloid isomers were deduced by comparing their fragment ions. Conclusion Chromatographie characters of 32 chemical compounds in Veratrum nigrum L. can be achieved in single run by UHPLC-Q-TOF/MS, which paves a way for further studying the metabolism and action mechanism of Veratrum nigrum L.

Veratrum patulum intoxication developed in a group of twenty-three patients / 대한내과학회지

Veratrum patulum is a perennial plant with toxicity, which grows wild in the high mountain areas of Korea. Various types of steroidal alkaloids contained in Veratrum patulum are known to cause symptoms such as nausea, vomiting, bradycardia and hypotension. Twenty-three patients were admitted to our center with chief complaints of nausea and vomiting after ingesting leaves of Veratrum patulum. The mean age of the group was 44 years old and was comprised of 19 males and 4 females. Some patients showed hypotension and bradycardia with symptoms such as dizziness. Ten patients with severe bradycardia coupled with other symptoms received atropine administration. Nausea and vomiting were improved after the administration of anti-emetics. Blood pressure and the pulse rate were all normalized on the day after admission, and all of the patients were discharged without any symptoms.

Study on the Change of the Content of Ginsenosides in the Decoction of Panax ginseng and Veratrum nigrum / 中国药房

OBJECTIVE:To study the change of the content of ginsenosides in the decoction of Panax ginseng and Veratrum nigrum and to find out the change regularity of chemical components in the compatibility of P. ginseng and V. nigrum so as to introduce the mechanism of "P. ginseng and V. nigrum are incompatible with each other" which derives from compatibility theory of Traditional Chinese Medicine. METHODS:HPLC was adopted to determine the content of ginsenoside in decoction derived from the combination of P. ginseng with different amounts of V. nigrum,and colorimetry was applied to determine the content of the total ginsenosides in herbal esidues. RESULTS:The content of the total ginsenosides decreased in the decoction as long as the content of V. nigrum increased. Nevertheless,the content of ginsenosides didn't change as amount of V. nigrum increased. CONCLUSION:It is reasonable to some extent that ginseng and veratrum nigrum are incompatible with each other. With the amount of V. nigrum increasing,the decrease of the total ginsenosides content doesn't result from some components in V. nigrum inhibiting the dissolution of ginsenoside in water solution but result from some components in V. nigrum reacting with ginsenoside leading to the reduction of ginsenoside.

Effects of Veratrum nigrum var. ussuriense alkaloids on platelet aggregation and time of coagulation and bleeding / 中草药

Object To study the effects of Veratrum nigrum L. var. ussuriense Nakai alkaloids (VnA) on platelet aggregation in rats and coagulation time, bleeding time in mice. Methods The antiplatelet effect of VnA was examined by determining platelet aggregation rate in normal rats and blood stasis model rats by turbidimetric method developed by Born. Whole blood coagulation time (CT) in mice was measured by capillary glass tube method, bleeding time (BT) by hemorrhagic transection of mouse tail model. Results VnA (45, 30, and 15 ?g/kg, iv) significantly inhibited ADP-induced platelet aggregation in rats in a dose-dependent manner. VnA (12.5, 25, 50, and 100 ?g/kg, ip) markedly increased CT and BT in mice. VnA [49.3 ?g/kg, which was anticoagulantly equieffective to heparin (1.25 mg/kg), ip] prolonged BT. There was no statistically significant difference in BT between VnA and heparin, although BT increase induced by VnA was shorter than that induced by heparin. Conclusion VnA has significant antiplatelet effect in rats and can prolong CT and BT in mice. At equieffective dose VnA-induced BT increase does not exceed that heparin induced.

Antithrombotic effects of Veratrum nigrum var.ussuriense alkaloids / 中草药

Object To investigate antithrombotic effects of Veratrum nigrum L.var ussuriense Nakai alkaloids ( Vn A) in rats. Methods The electrically induced rat carotid artery thrombosis model was used to examine the antiarterial thrombosis effect of Vn A using occlusion time( OT) of carotid artery as phar- macologic index;the stasis- induced inferior vena cava thrombosis model was used to evaluate antivenous thrombosis effectof Vn A in terms of thrombosis formation rate and decrease in thrombus dry weight.Re- sults The iv administration of Vn A( 7.2— 42 .9) ?g/kg to rats resulted in a dose- dependent effect and significantprolongation in OT. Vn A at the dose of 30?g/kg produced an antiarterial thrombosis effecte- qual to thatof LAS( 1 8.0 mg/kg) .Also,a single bolus iv Vn A( 30 ?g/kg) increased OT in a time- depen- dentmanner;the antiarterial thrombosis effectwas rapid in onsetand lasted atleast80 min,and peaked at 1 5 min postdosing.Vn A( 1 5— 45 ?g/kg iv) decreased the thrombus dry weight significantly and dose- de- pendently. Conclusion Vn A has powerful inhibitory effects againstboth arterial and venous thrombosis in rats and acts in a dose- and time- dependentmanner.Its effective dose is as low as?g perkg body weightof rats.The finding of the Vn A antithrombotic effeets reveal a bright future of its R &D.

Antithrombotic effect of verussurinine from Veratrum nigrum var. ussuriense alkaloids / 中草药

Objective To study the effects of verussurinine (VSRN), an alkaloid isolated from Veratrum nigrum var. ussuriense alkaloids (VnA), against thrombosis and its platelet aggregation inhibitory activity in rats in order to find out whether VSRN is the antithrombotic active ingredient of VnA. Methods The electrically induced rat carotid artery thrombosis and stasis-induced rat inferior vena cava thrombosis models were used to evaluate the anti-arterial and anti-venous thrombosis effect of VSRN, respectively. Borns turbidimetric method was used to examine the in vivo and in vitro anti-platelet effect so as to investigate the antiplatelet aggregation of VSRN. Results In comparison with saline, VSRN in five different doses (1.25—20.00 ?g/kg) showed significantly and dose-dependently prolonged occlusion time (OT) of carotid artery injured by electrical stimulation and reduced thrombus dry weight of inferior vena cava ligated for 4 h to cause stasis. Platelet aggregation was found to be inhibited by VSRN in the doses of 1.25—5.00 ?g/kg and at the concentration of 6.25—50 ?g/L in both in vivo and in vitro test. Conclusion VSRN has powerful arteriovenous antithrombosis and antiplatelet aggregation of rats. The antithrombotic effect of VSRN is related to its platelet aggregation inhibitory activity. The above findings indicate that VSRN is an antithrombotic active ingredient of VnA.