ABSTRACT
BACKGROUND: Older age, renal dysfunction and low left ventricular ejection fraction are accepted predictors of poor outcome in patients with infective endocarditis (IE). This study aimed to investigate the prognostic significance of the age, creatinine and ejection fraction (ACEF) score in IE. METHODS: The study involved 1019 IE patients, who were classified into three groups according to the tertiles of ACEF score: low ACEF (<0.6, n = 379), medium ACEF (0.6-0.8, n = 259) and high ACEF (>0.8, n = 381). The ACEF score was calculated as follows: age (years)/ejection fraction (%)+1 (if serum creatinine value was >2 mg/dL). The relationship between ACEF score and adverse events was analyzed. RESULTS: In-hospital mortality was 8.2%, which increased with the increase of ACEF score (4.2% vs. 5.0% vs. 14.4% for the low-, medium- and high-ACEF groups, respectively; P < 0.001). ACEF score had a good discriminative ability for predicting in-hospital death [areas under the curve (AUC), 0.706, P < 0.001]. The predictive value of ACEF score in surgical treatment was significantly higher than in conservative treatment for predicting in-hospital death (AUC, 0.812 vs. 0.625; P = 0.001). Multivariable analysis revealed that ACEF score was independently associated with in-hospital mortality (adjusted odds ratio, 2.82; P < 0.001) and long-term mortality (adjusted hazard ratio, 2.51; P < 0.001). CONCLUSION: ACEF was an independent predictor for in-hospital and long-term mortality in IE patients, and it could be considered as a useful tool for risk stratification. ACEF score was more suitable for surgical patients in terms of assessing the risk of in-hospital mortality.
Subject(s)
Age Factors , Creatinine/blood , Endocarditis/mortality , Endocarditis/physiopathology , Hospital Mortality/trends , Stroke Volume , Aged , Endocarditis/therapy , Female , Humans , Logistic Models , Male , Middle Aged , Multivariate Analysis , Predictive Value of Tests , Prognosis , Retrospective Studies , Risk Assessment/methods , Risk Factors , Survival AnalysisABSTRACT
AIM: Diabetes is a risk factor in infective endocarditis. However, few studies have focused on the prognostic value of prediabetes in infective endocarditis. This analysis aimed to explore the relationship between prediabetes and outcomes for people with infective endocarditis. METHODS: Diabetes and prediabetes definitions were based on the American Diabetes Association 2014 criteria. A total of 866 people who had been consecutively diagnosed with infective endocarditis between January 2009 and July 2015 were included in the analysis. They were divided into three groups: normoglycaemia (n = 469), prediabetes (n = 246) and diabetes (n = 151). Univariate and multivariate analyses were used to identify risk factors for adverse outcomes. RESULTS: Overall in-hospital mortality was 8.5% (74 of 866), and differed significantly among the normoglycaemia, prediabetes and diabetes groups (3.4%, 12.6% and 17.9%, respectively; P < 0.001). Compared with the normoglycaemia group, the adjusted odds ratio for in-hospital death was 2.42 [95% confidence interval (CI) 1.11-5.31; P = 0.027) for prediabetes and 3.39 (95% CI 1.48-7.80; P = 0.004) for diabetes. The cumulative long-term death rate was significantly higher in the prediabetes or diabetes groups than in the normoglycaemia group (log-rank = 34.82; P < 0.001). CONCLUSION: In addition to diabetes, prediabetes was also associated with a higher risk of in-hospital and long-term mortality among people with infective endocarditis. Therefore, attention should be paid to this population.
Subject(s)
Diabetes Mellitus/diagnosis , Endocarditis/diagnosis , Endocarditis/mortality , Prediabetic State/diagnosis , Adult , Aged , Comorbidity , Diabetes Mellitus/mortality , Diabetic Angiopathies/diagnosis , Diabetic Angiopathies/mortality , Endocarditis/complications , Female , Hospital Mortality , Humans , Male , Middle Aged , Prediabetic State/complications , Prediabetic State/mortality , Prognosis , Risk FactorsABSTRACT
To investigate the effects of a synthetic soybean isoflavone (ISF) on growth performance, meat quality, and antioxidation in male broilers, 1,500 birds that were 42 d old were allotted to 5 treatments with 6 replicates per treatment (50 birds per replicate). Birds were fed diets supplemented with 0, 10, 20, 40, or 80 mg of ISF/kg, respectively, for a period of 3 wk ad libitum. The results showed that dietary supplementations with 10 or 20 mg of ISF/kg increased weight gain by 13.6 and 16.2% (P < 0.01) and elevated feed intake by 7.37% (P < 0.05) and 11.2% (P < 0.01), respectively. Addition of 10 mg of ISF/kg decreased feed:gain by 5.5% (P < 0.05). Supplementation with 40 mg of ISF/kg in the diet slightly increased water-holding capacity by 17.24% (P < 0.1), and the addition of 20 or 40 mg/kg of ISF significantly increased the pH value of meat (P < 0.01), although adding 40 or 80 mg of ISF/kg increased the lightness of meat color (P < 0.05). Malondialdehyde production was slightly reduced in plasma of 20 mg of ISF/kg supplemented chickens (P < 0.1) and significantly decreased in breast muscles of 20, 40, or 80 mg of ISF/kg supplemented chickens (P < 0.01). The addition of 40 or 80 mg of ISF/kg significantly increased total antioxidant capability (P < 0.01) and slightly elevated total superoxide dismutase activity (P < 0.1) in plasma of chickens. The dose of 80 mg of ISF/kg slightly improved catalase activity in plasma (P < 0.06). In breast muscle, treatment of birds with 40 or 80 mg of ISF/kg caused an increase of total superoxide dismutase activity by 25.36% (P < 0.05) or 63.93% (P < 0.01). Catalase activity significantly increased by 70.61% by the supplemental ISF at the 40-mg level (P < 0.05). Also, 10, 20, or 40 mg doses of ISF/kg decreased lactic acid production (P < 0.05). The results of this study indicate that dietary ISF could improve growth performance and meat quality by decreasing lipid peroxidation and improving antioxidative status in male broilers.
Subject(s)
Antioxidants/metabolism , Chickens/growth & development , Chickens/metabolism , Glycine max/chemistry , Isoflavones/pharmacology , Meat/standards , Animal Feed , Animal Nutritional Physiological Phenomena , Animals , Diet/veterinary , Dietary Supplements , Isoflavones/chemistry , Lipid Peroxidation/drug effects , MaleABSTRACT
The new compound (R)-4-phenyl-2-O-[beta-d-xylopyranosyl(1 --> 6)-beta-D-glucopyranosyl]butane (1) and its epimer (2), together with (R)-4-phenyl-2-O-beta-D-glucopyranosyl butane (24) and (S)-4-phenyl-2-O-beta-D-glucopyranosyl butane (25) were firstly synthesized from 4-phenylbutan-2-one and glucose. The absolute configuration of C-2 for 1 was confirmed as R. Their anti-tumour activities were evaluated.
Subject(s)
Antineoplastic Agents, Phytogenic/chemical synthesis , Butanes/chemical synthesis , Disaccharides/chemical synthesis , Rhododendron/chemistry , Cell Line, Tumor , Humans , StereoisomerismABSTRACT
Three well-known natural diosgenyl glycosides which have the same sugar chains but different sequence, ophipogonin C', polyphillin C and prosapogenin B, were synthesised by a facile approach. A method using the levulinyl group as a protecting group to selectively mask the C3-OH of diosgenyl 4,6-O-benzylidene-beta-D-glucopyranoside is described.
Subject(s)
Diosgenin/analogs & derivatives , Diosgenin/chemical synthesis , Glycosides/chemical synthesis , Chromatography, Thin Layer , Magnetic Resonance Spectroscopy , Mass Spectrometry , Molecular StructureABSTRACT
Martentoxin is a peptide of 37 amino acid residues purified from the venom of the Chinese scorpion Buthus martensi Karch, which has been demonstrated to be an inhibitor of voltage-dependent sodium channel and voltage-dependent delayed rectifier potassium channel. To elucidate the molecular mechanism of this interaction, the structure of martentoxin was studied by 2D-NMR. The secondary structure of martentoxin consists of a triple-stranded beta-sheet connected to a alpha-helical structure. This helix encompasses 10 residues from Ser11 to Lys20. The three strands of beta-sheet probably comprise residues Gly2-Asp5, Q27-N30 and Glu33-Cys36, Cys30-Asn33 with a type I'beta turn centered on Asn31-Asn32. The results indicate that martentoxin possesses the conserved beta alpha beta beta structure of all the potassium channel toxins.
Subject(s)
Scorpion Venoms/chemistry , Scorpions/chemistry , Amino Acid Sequence , Animals , Hydrogen Bonding , Magnetic Resonance Spectroscopy , Molecular Conformation , Molecular Sequence DataABSTRACT
An efficient method for the synthesis of the natural product (+)-(R)-butyl ester of rosmarinic acid (+)-(R)-1 and its enantiomer ( - )-(S)-1 has been developed by chemical resolution of its phenyl lactic acid precursors 4 with ( - )-menthol. Their antioxidative and anti-tumor activities were evaluated.
Subject(s)
Antineoplastic Agents, Phytogenic/chemical synthesis , Antineoplastic Agents, Phytogenic/pharmacology , Antioxidants/chemical synthesis , Antioxidants/pharmacology , Cinnamates/chemical synthesis , Cinnamates/pharmacology , Depsides/chemical synthesis , Depsides/pharmacology , Isodon/chemistry , Animals , Cell Line, Tumor , Drug Screening Assays, Antitumor , Esters/chemical synthesis , Esters/pharmacology , Humans , In Vitro Techniques , Lactic Acid/chemistry , Lipid Peroxidation/drug effects , Magnetic Resonance Spectroscopy , Menthol/chemistry , Microsomes, Liver/drug effects , Microsomes, Liver/metabolism , Molecular Conformation , Rats , Solvents , Spectrometry, Mass, Electrospray Ionization , Spectrometry, Mass, Fast Atom Bombardment , Tetrazolium Salts , Thiazoles , Rosmarinic AcidABSTRACT
Anew peptide, designated as Buthus martensi Karch (BmK) AngM1, with an isoelectric point (pI) of 5.8 was purified and characterized from the venom of Buthus martensi Karch. The molecular mass was calculated as 7040.5 Da from multiple-charged ions by elelctrospray ionization mass spectroscopy (ESI/MS). The complete amino acid sequence of BmK AngM1 of 64 amino acid residues was determined by automatic sequencing of N-terminal part of the native peptide and the fragments of reduced and S-carboxymethylated (RCM)-peptide degraded by Staphylococcus aureaus V(8) protease and TPCK(N-p-Tosyl-L-phenylalanine chloromethyl ketone)-treated trypsin. Bioactivity tested using mouse-twisting model showed an evident analgesic effect with 63.0% (P < 0.001) inhibition efficiency at the dose of 0.8 mg/kg, but the LD(50) was larger than 50 mg/kg. Electrophysiological studies showed that BmK AngM1 at the concentration of 1 microm obviously inhibit voltage-dependent Na(+) current (I(Na)) and voltage-dependent delayed rectifier K(+) current (I(K)) but had no effects on transient K(+) current.
Subject(s)
Analgesics, Non-Narcotic/chemistry , Analgesics, Non-Narcotic/isolation & purification , Peptides/chemistry , Peptides/isolation & purification , Scorpion Venoms/chemistry , Amino Acid Sequence , Analgesics, Non-Narcotic/toxicity , Animals , Male , Membrane Potentials/drug effects , Mice , Neurons/physiology , Peptides/toxicity , Potassium/metabolism , Rats , Rats, Wistar , Scorpions/chemistry , Sodium/metabolism , Spectrometry, Mass, Electrospray IonizationABSTRACT
A new peptide named Martentoxin I and an analogue Martentoxin were purified and characterized from the venom of Buthus martensi Karch. Martentoxin I consisted of 36 amino acid residues with molecular mass as 3908.0 Da determined by matrix-assisted laser desorption ionization time-of-flight-MS. The amino acid sequence was determined as GLIDVKCFASSECWTACKKVTGSGQGKCQNNQCRCY by Edman degradation. Martentoxin consisted of 37 amino acid residues with a molecular mass as 4055.3 Da and it showed highly sequence identity to Martentoxin I as FGLIDVKCFASSECWTACKKVTGSGQGKCQNNQCRCY. Estimation from circular dichroism spectra indicated Martentoxin I owned 18.0% alpha-helix, 53.0% beta-sheet structure and 3.9% turn while Martentoxin contained 13.3% alpha-helix, 64.3% beta-sheet structure and 1.1% turn. The toxicity assay showed both peptides had no toxic effects on mice up to the dose of 10 mg/kg. Electrophysiological studies showed that Martentoxin I and Martentoxin at the concentration of 1 microm significantly inhibited voltage-dependent Na+ current (INa) and voltage-dependent delayed rectifier K+ current (IK) but had no effects on transient K+ current (IA). Both interactions with Na+ and K+ channels were irreversible.
Subject(s)
Peptides/chemistry , Peptides/isolation & purification , Scorpion Venoms/chemistry , Scorpion Venoms/isolation & purification , Scorpions/chemistry , Amino Acid Sequence , Animals , Circular Dichroism , Electrophysiology , Male , Membrane Potentials/drug effects , Mice , Molecular Sequence Data , Molecular Weight , Peptides/toxicity , Potassium/metabolism , Rats , Rats, Wistar , Scorpion Venoms/toxicity , Sodium/metabolism , Structure-Activity RelationshipABSTRACT
Five new diprenylated flavonols, broussonol A (1), broussonol B (2), broussonol C (3), broussonol D (4), and broussonol E (5), along with two known compounds, were isolated from an ethanolic extract of the leaves of Broussonetia kazinoki. Their structures were elucidated by chemical and spectral methods. Cytotoxic activities were evaluated against several different cell lines.
Subject(s)
Flavonoids/isolation & purification , Moraceae/chemistry , Dose-Response Relationship, Drug , Drug Screening Assays, Antitumor , Flavonoids/chemistry , Flavonoids/pharmacology , Humans , Ileal Neoplasms , KB Cells , Lung Neoplasms , Magnetic Resonance Spectroscopy , Medicine, Chinese Traditional , Molecular Conformation , Molecular Structure , Plant Leaves/chemistry , Plants, Medicinal/chemistry , Spectrophotometry, Infrared , Spectrophotometry, Ultraviolet , Tumor Cells, Cultured/drug effectsABSTRACT
Two new bislabdane-type diterpenoids lanceolatin (1), lancelatol (2) and three new diterpenoids 15-nor-14-oxo-8(17),12-labdanien-14,18-dionic acid (3), 8(17),12,14-labdantrien-18-oic acid (4) and 8(17),12,14-labdantrien-18-ol (5), together with 7 known diterpenoids were isolated from the roots of Cunninghamia lanceolata. Their structures were determined by spectroscopic and chemical methods. All of these compounds were isolated from the species for the first time. One of the isolated compounds showed a significant inhibition effect on mouse hind-paw edema induced by carrageenan.
Subject(s)
Cycadopsida/chemistry , Diterpenes/isolation & purification , Drugs, Chinese Herbal/chemistry , Animals , Anti-Inflammatory Agents, Non-Steroidal/chemistry , Anti-Inflammatory Agents, Non-Steroidal/isolation & purification , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Cycadopsida/therapeutic use , Diterpenes/chemistry , Drugs, Chinese Herbal/therapeutic use , Edema/chemically induced , Edema/drug therapy , Magnetic Resonance Spectroscopy , Mice , Molecular Structure , Phytotherapy , Plant Roots/chemistryABSTRACT
A steroidal saponin, named tuberoside, together with seven known compounds, were isolated from the seeds of Allium tuberosum Rottl. ex Spreng. Its structure was established by spectroscopic data, hydrolysis, and comparison with spectral data of known compounds to be (2alpha, 3beta, 5alpha, 25S)-2,3,27-trihydroxyspirostane 3-O-alpha-L-rhamnopyranoyl-(1-->2)-O-[alpha-L-rhamnopyranoyl-(1-->4)]-beta-D-glucopyranoside.
Subject(s)
Allium/chemistry , Saponins/isolation & purification , Steroids/isolation & purification , Magnetic Resonance Spectroscopy , Medicine, Chinese Traditional , Phytotherapy , Saponins/chemistry , Seeds/chemistry , Steroids/chemistryABSTRACT
A novel alkaloid, chestnutamide, was isolated from the flowers of Castanea mollissima Blume. The structure was determined on the basis of spectral analysis.
Subject(s)
Fagaceae/chemistry , Indole Alkaloids/isolation & purification , Pyrrolizidine Alkaloids/isolation & purification , China , Drugs, Chinese Herbal/chemistry , Indole Alkaloids/chemistry , Magnetic Resonance Spectroscopy , Molecular Structure , Plant Stems/chemistry , Plants, Medicinal/chemistry , Pyrrolizidine Alkaloids/chemistryABSTRACT
Two new benzofuran derivatives, macrourins A (1) and B (2), together with two known stilbene derivatives, were isolated from the barks of Morus macroura Miq. Their structures were elucidated by means of spectroscopic evidence.
Subject(s)
Benzofurans/chemistry , Trees/chemistry , Benzofurans/isolation & purification , China , Chromatography, Gel , Drugs, Chinese Herbal/chemistry , Gas Chromatography-Mass Spectrometry , Magnetic Resonance Spectroscopy , Optical Rotation , Plant Bark/chemistry , Spectrophotometry, Infrared , Spectrophotometry, UltravioletABSTRACT
20 compounds were isolated from the leaves of Magnolia denudata including 16 lignans, which belong to 6 structural types. Except for (7R, 8S, 1'S)-delta8' -1', 4'- dihydro-5'-methoxy-3,4-methylenedioxy-4'-oxo-7.0.2', 8.1'-neolignan (6), magliflonenone (9), 2, 5'-diene-2', 8'-epoxy-5'-methoxy-8-methyl-4'-oxo-3,4- methylenedioxy-spiro (5, 5)-undecane (10), veraguensin (16) and beta-sitosterol (20), the other 15 compounds were obtained from this species for the first time. The absolute configurations of 3 compounds (1, 4, 10) were determined by CD spectroscopy for the first time. The anti-inflammatory activities of compounds 1, 2 and 16 were assessed and 2 was shown to have significant inhibition effect on mice hind-paw edema induced by carrageenan.
Subject(s)
Anti-Inflammatory Agents/isolation & purification , Benzofurans/isolation & purification , Lignans/isolation & purification , Magnoliaceae/chemistry , Animals , Anti-Inflammatory Agents/chemistry , Anti-Inflammatory Agents/pharmacology , Benzofurans/chemistry , Benzofurans/pharmacology , China , Edema/drug therapy , Gas Chromatography-Mass Spectrometry , Lignans/chemistry , Lignans/pharmacology , Mice , Nuclear Magnetic Resonance, Biomolecular , Optical Rotation , Plant Extracts/chemistry , Plant Extracts/isolation & purification , Plant Leaves/chemistry , Spectrophotometry, InfraredABSTRACT
Five new annonaceous acetogenins, calamistrins C-G (1-5), were isolated from an ethanolic extract of the roots of Uvaria calamistrata. Compounds 1-3 were mono-THF ring acetogenins; compounds 4 and 5 were bis-THF acetogenins, with the THF rings from C-18 to C-25. The absolute configurations of 3, 4, and 5 as well as the partial absolute configurations of 1 and 2 were determined by (13)C NMR spectroscopy and advanced Mosher methodology.
Subject(s)
Furans/isolation & purification , Lactones/isolation & purification , Magnoliopsida/chemistry , Drug Screening Assays, Antitumor , Furans/chemistry , Furans/pharmacology , Humans , Lactones/chemistry , Lactones/pharmacology , Molecular Structure , Plant Roots/chemistry , Tumor Cells, CulturedABSTRACT
Two novel gamma-lactones, saccopetrin C(1) and saccopetrin D (2), were isolated from the roots of Saccopetalum prolificum. Their structures were established by spectroscopic and chemical methods.
Subject(s)
Lactones/isolation & purification , Magnoliopsida/chemistry , China , Lactones/chemistry , Magnetic Resonance Spectroscopy , Molecular Structure , Plant Roots/chemistryABSTRACT
AIM: To investigate the chemical constituents of Murraya kwangsiensis. METHODS: Compounds were isolated by silica gel column chromatography and TLC method, respectively. Structures of compounds were elucidated by spectral (UV, IR, MS, 1HNMR and 13CNMR) analysis. RESULTS: Five carbazole alkaloids and two other compounds were isolated and identified. Six of them are known compounds: murrayafoline A, murrayanine, koenine, isomahanine, palmitic acid and beta-sitosterol. One is a new alkaloid, named kwangsine. CONCLUSION: A new alkaloid, named kwangsine, was isolated from Murraya kwangsiensis Var. Six known compounds were isolated from this plant for the first time.