Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 9 de 9
Filtrar
1.
J Ethnopharmacol ; 266: 113432, 2021 Feb 10.
Artículo en Inglés | MEDLINE | ID: mdl-33011367

RESUMEN

ETHNOPHARMACOLOGICAL RELEVANCE: Veronica ciliata Fisch. is a traditional medical herb that present in more than 100 types of Tibetan medicine prescriptions, most of which are used for liver disease therapy. Iridoid glycosides have been identified as the major active components of V.ciliata with a variety of biological activities. AIMS OF THE STUDY: The aim of this study is to explore the protective effect and potential mechanism of n-Butanol extract (BE) and iridoid glycosides (IG) from V.ciliata against ɑ-naphthyl isothiocyanate (ANIT)-induced hepatotoxicity and cholestasis in mice. MATERIALS AND METHODS: Mice were intragastrically (i.g.) given BE and IG at different dose or positive control ursodeoxycholic acid (UCDA) once a day for 14 consecutive days, and were treated with ANIT to cause liver injury on day 12th. Serum levels of hepatic injury markers and cholestasis indicators, liver index and liver histopathology were measured to evaluate the effect of BE and IG on liver injury caused by ANIT. The protein levels of tumor necrosis factor-α (TNF-α), nuclear factor kappa B(NF-κB), interleukin-6 (IL-6), Na+/taurocholate cotransporting polypeptide (NTCP), bile salt export pump (BSEP), multidrug resistance-associated protein 2 (MRP2), and the levels of oxidative stress indicators in liver tissue were investigated to reveal the underlying protective mechanisms of BE and IG against ANIT-induced hepatotoxicity and cholestasis. RESULTS: The n-Butanol extract (BE) and iridoid glycosides (IG) isolated from V.ciliata significantly decreased serum level of cholestatic liver injury markers aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (ALP), γ-glutamyl transferase (GGT), total bile acid (TBA), total bilirubin (TBIL), and direct bilirubin (DBIL) in ANIT-treated mice. Histopathology of the liver tissue showed that pathological damages were relieved upon BE and IG treatment. Meanwhile, the results indicated BE and IG notably restored relative liver weights, inhibited oxidative stress induced by ANIT through increasing hepatic level of superoxide dismutase (SOD), reduced glutathione (GSH), catalase (CAT) and decreasing hepatic content of malondialdehyde (MDA). Western blot revealed that BE and IG inhibited the expression of pro-inflammatory factors TGF-α, IL-6 and NF-κB. Furthermore, the decreased protein expression of bile acid transporters NTCP, BSEP, MRP2 were upregulated by BE and IG in a dose-dependent manner. CONCLUSION: The results have demonstrated that BE and IG exhibited a dose-dependently protective effect against ANIT-induced liver injury with acute intrahepatic cholestasis in mice, which might be related to the regulation of oxidative stress, inflammatory response and bile acid transport. In addition, these findings pointed out that iridoid glycosides as main active components of V.ciliata play a critical role in hepatoprotective effect of V.ciliata.


Asunto(s)
Colestasis/tratamiento farmacológico , Glicósidos Iridoides/farmacología , Extractos Vegetales/farmacología , Veronica/química , 1-Butanol/química , 1-Naftilisotiocianato , Animales , Ácidos y Sales Biliares/metabolismo , Transporte Biológico/efectos de los fármacos , Colestasis/fisiopatología , Modelos Animales de Enfermedad , Relación Dosis-Respuesta a Droga , Glicósidos Iridoides/administración & dosificación , Glicósidos Iridoides/aislamiento & purificación , Hígado/efectos de los fármacos , Hígado/patología , Masculino , Medicina Tradicional Tibetana , Ratones , Estrés Oxidativo/efectos de los fármacos , Extractos Vegetales/administración & dosificación
2.
J Sep Sci ; 43(2): 406-417, 2020 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-31633862

RESUMEN

Zhi-Zi-Hou-Po Decoction, consisting of Gardenia jasminoides Ellis, Magnolia officinalis Rehd. et Wils., and Citrus aurantium L, is a classical Traditional Chinese Medicine formula for the treatment of depression. In order to make good and rational use of this formula in the future, a sensitive, selective, and reliable ultra high performance liquid chromatography with tandem mass spectrometry method was developed for simultaneous determination of two iridoid glycosides (geniposide and genipin gentiobioside), two lignans (honokiol and magnolol), four flavonoid glycosides (isonaringin, naringin, hesperidin, and neohesperidin), the major bioactive constituents of Zhi-Zi-Hou-Po Decoction, in rat plasma using paeoniflorin as internal standard. Plasma samples were pretreated by a simple protein precipitation with acetonitrile. Chromatographic separation was performed on a shim-pack XR-ODS C18 column (75 × 3.0 mm, 2.2 µm) using gradient elution with mobile phase consisting of 0.1% formic acid aqueous solution and acetonitrile at a flow rate of 0.5 mL/min. Mass spectrometric detection was conducted on a 3200 QTRAP mass spectrometry equipped with electrospray ionization source in negative ionization mode. Quantification was performed using multiple reactions monitoring mode. Calibration curves exhibited good linearity (r > 0.9947) over a wide concentration range for all analytes, and the lower limits of quantification were 10, 5, 1, 5, 1, 5, 1, and 5 ng/mL for geniposide, genipin gentiobioside, honokiol, magnolol, isonaringin, naringin, hesperidin, and neohesperidin, respectively. The intraday and interday precisions at three quality control levels were less than 12.3% and the accuracies ranged from -11.2 to 10.7%. Extraction recovery, matrix effect, and stability were satisfactory in rat plasma. The validated method was successfully applied to a pharmacokinetic study of the eight analytes after oral administration of Zhi-Zi-Hou-Po decoction to rats.


Asunto(s)
Medicamentos Herbarios Chinos/farmacocinética , Flavonoides/farmacocinética , Glicósidos Iridoides/farmacocinética , Lignanos/farmacocinética , Administración Oral , Animales , Cromatografía Líquida de Alta Presión , Medicamentos Herbarios Chinos/administración & dosificación , Medicamentos Herbarios Chinos/análisis , Flavonoides/administración & dosificación , Flavonoides/sangre , Glicósidos Iridoides/administración & dosificación , Glicósidos Iridoides/sangre , Lignanos/administración & dosificación , Lignanos/sangre , Masculino , Medicina Tradicional China , Estructura Molecular , Ratas , Ratas Sprague-Dawley , Espectrometría de Masas en Tándem
3.
Curr Med Sci ; 40(6): 1031-1039, 2020 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-33428130

RESUMEN

rTg4510 mice are transgenic mice expressing P301L mutant tau and have been developed as an animal model of tauopathies including Alzheimer's disease (AD). Besides cognitive impairments, rTg4510 mice also show abnormal hyperactivity behavior. Cornel iridoid glycoside (CIG) is an active ingredient extracted from Cornus officinalis, a traditional Chinese herb. The purpose of the present study was to investigate the effects of CIG on the emotional disorders such as hyperactivity, and related mechanisms. The emotional hyperactivity was detected by locomotor activity test and Y maze test. Immunofluorescent and immunohistochemical analyses were conducted to measure neuron loss and phosphorylated tau. Western blotting was used to detect the expression of related proteins. The results showed that intragastric administration of CIG for 3 months decreased the hyperactivity phenotype, prevented neuronal loss, reduced tau hyperphosphorylation and aggregation in the amygdala of rTg4510 mice. Meanwhile, CIG alleviated the synaptic dysfunction by increasing the expression of N-methyl-D-aspartate receptors (NMDARs) subunits GluN1 and GluN2A and αamino-3-hydroxy-5-methyl-4-isoxazole propionic acid receptor (AMPAR) subunits GluA1 and GluA2, and increased the level of phosphorylated Ca2+/calmodulin dependent protein kinase II α (p-CaMK IIα) in the brain of rTg4510 mice. In conclusion, CIG may have potential to treat the emotional disorders in tauopathies such as AD through reducing tau pathology and improving synaptic dysfunction.


Asunto(s)
Cornus/química , Glicósidos Iridoides/administración & dosificación , Tauopatías/tratamiento farmacológico , Proteínas tau/genética , Proteínas tau/metabolismo , Animales , Modelos Animales de Enfermedad , Femenino , Humanos , Glicósidos Iridoides/farmacología , Masculino , Aprendizaje por Laberinto/efectos de los fármacos , Ratones , Ratones Transgénicos , Mutación , Proteínas del Tejido Nervioso/metabolismo , Fenotipo , Fosforilación/efectos de los fármacos , Extractos Vegetales/química , Distribución Aleatoria , Receptores de N-Metil-D-Aspartato/metabolismo , Tauopatías/genética , Tauopatías/metabolismo , Tauopatías/psicología , Resultado del Tratamiento
4.
BMC Complement Altern Med ; 18(1): 288, 2018 Oct 24.
Artículo en Inglés | MEDLINE | ID: mdl-30355303

RESUMEN

BACKGROUND: Iridoid glycosides (IGs), including monotropein (MON) and deacetyl asperulosidic acid (DA) as the main ingredients, are the major chemical components in Morinda officinalis How. (MO) root, possessing various pharmacological properties including anti-osteoporosis, anti-inflammation and anti-rheumatism activities.The aim of the present study was to further elucidate the pharmacological actions of MO by investigating the pharmacokinetics and tissue distribution of IGs in MO. METHODS: An ultra high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS) method was developed and validated for simultaneous determination of MON and DA levels in plasma and various tissues of Wistar rats. MON, DA and acetaminophen (ACE) as the internal standard (IS) were extracted from rat plasma and tissue samples by direct deproteinization with methanol. The rats were administered orally at 1650 mg/kg MO and 25, 50 and 100 mg/kg MO iridoid glycosides (MOIGs) or intravenously at MOIG 25 mg/kg for pharmacokinetic study of MON and DA. In addition, 100 mg/kg MOIG was administered orally for tissue distribution study of MON and DA. Non-compartmental pharmacokinetic profiles were constructed. Tissue distributions were calculated according to the validated methods. RESULTS: Significant differences in the pharmacokinetic parameters were observed in male and female rats. The AUC0-t, Cmax and bioavailability of MON and DA in female rats were higher than those in male rats. MON and DA mainly distributed in the intestine and stomach after oral administration, and noteworthily high concentrations of MON and DA were detected in the rat hypothalamus. CONCLUSION: The results of the present study may shed new lights on the biological behavior of MOIGs in vivo, help explain their pharmacological actions, and provide experimental clues for rational clinical use of these IGs extracted from the MO root.


Asunto(s)
Medicamentos Herbarios Chinos/farmacocinética , Glicósidos/farmacocinética , Iridoides/farmacocinética , Morinda/química , Administración Oral , Animales , Medicamentos Herbarios Chinos/administración & dosificación , Medicamentos Herbarios Chinos/química , Femenino , Glicósidos/administración & dosificación , Glicósidos/química , Glicósidos Iridoides/administración & dosificación , Glicósidos Iridoides/química , Glicósidos Iridoides/farmacocinética , Iridoides/administración & dosificación , Iridoides/química , Masculino , Estructura Molecular , Raíces de Plantas/química , Ratas , Ratas Wistar , Espectrometría de Masas en Tándem , Distribución Tisular
5.
Biomed Res Int ; 2016: 6725381, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-27990434

RESUMEN

Purpose. This study was to investigate the effects of cornel iridoid glycoside (CIG) on spinal cord injury (SCI) in rats. Methods. The thoracic cord (at T9) of rats was injured by clip compression for 30 sec. Locomotor function was assessed using the Basso, Beattie, and Bresnahan (BBB) rating scale. Neuroanatomic stereological parameters as well as Nogo-A, p75 neurotrophin receptor (p75NTR), and ROCKII expression were measured by histological processing, immunohistochemistry, and stereological analyses. The axons passing through the lesion site were detected by BDA tracing. Results. Intragastric administration of CIG (60 and 180 mg/kg) improved the locomotor impairment at 10, 17, 24, and 31 days post-injury (dpi) compared with untreated SCI model rats. CIG treatment decreased the volume of the lesion epicenter (LEp) and increased the volume of spared tissue and the number of surviving neurons in the injured spinal cord at 31 dpi. CIG promoted the growth of BDA-positive axons and their passage through the lesion site and decreased the expression of Nogo-A, p75NTR, and ROCKII both in and around the LEp. Conclusion. CIG improved the locomotor impairment, decreased tissue damage, and downregulated the myelin-associated inhibition signaling pathway in SCI rats. The results suggest that CIG may be beneficial for SCI therapy.


Asunto(s)
Medicamentos Herbarios Chinos/administración & dosificación , Glicósidos Iridoides/administración & dosificación , Traumatismos de la Médula Espinal/tratamiento farmacológico , Médula Espinal/efectos de los fármacos , Animales , Axones/efectos de los fármacos , Axones/patología , Cornus/química , Medicamentos Herbarios Chinos/química , Regulación de la Expresión Génica/efectos de los fármacos , Humanos , Glicósidos Iridoides/química , Locomoción/efectos de los fármacos , Vaina de Mielina/efectos de los fármacos , Vaina de Mielina/genética , Proteínas del Tejido Nervioso , Proteínas Nogo/biosíntesis , Ratas , Receptores de Factores de Crecimiento , Receptores de Factor de Crecimiento Nervioso/biosíntesis , Transducción de Señal/efectos de los fármacos , Médula Espinal/fisiopatología , Traumatismos de la Médula Espinal/genética , Traumatismos de la Médula Espinal/patología , Quinasas Asociadas a rho/biosíntesis
6.
Anal Bioanal Chem ; 408(21): 5723-5735, 2016 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-27342796

RESUMEN

In this study, a novel untargeted metabolomics-driven strategy based on LC-MS was used to rapidly screen and identify the absorbed components and metabolites of Zhi-Zi-Hou-Po decoction (ZZHPD) in rat plasma. The plasma sample was obtained from orbital venous of rats after oral administration and pretreated by protein precipitation before analysis. All sample data from total ion chromatograms (TICs) of LC-TOF/MS were aligned and peak picked by XCMS and MetAlign combined to extract three-dimensional datasets (peak code, t R -m/z pairs and ion intensity). Xenobiotics in rat plasma were differentiated from endogenous components by multivariate statistical analysis and then divided into prototype compounds and metabolites by comparing t R -m/z with the chemical compounds of ZZHPD. Combined with fragment ions and structure information of LC-TSQ/MS, a total of 61 compounds, including 35 prototype compounds and 26 metabolites, were rapidly identified or tentatively characterized in rat plasma. Results indicated that iridoid glycosides, monoterpenoids, flavonoids, and lignans were the main absorbed chemical components of ZZHPD. Glucuronidation and sulfation were the main metabolic pathways of ZZHPD compounds in vivo. In addition, there were ring-opening reactions and reduction reactions for iridoid glycosides, hydrolysis for flavonoids, as well as hydroxylation and stereoscopic conversion reactions for lignans. This study offers a systematically applicable approach for rapid screening and identification of xenobiotics and metabolites derived from multi-herb prescription in vivo, and provides useful information for ascertaining bioactive ingredients and action mechanisms of ZZHPD. Graphical Abstract Diagram of untargeted metabolomics-driven strategy for ZZHPD in rat plasma.


Asunto(s)
Antidepresivos/metabolismo , Medicamentos Herbarios Chinos/metabolismo , Metabolómica/métodos , Administración Oral , Animales , Antidepresivos/administración & dosificación , Antidepresivos/sangre , Cromatografía Liquida/métodos , Medicamentos Herbarios Chinos/administración & dosificación , Medicamentos Herbarios Chinos/farmacocinética , Flavonoides/administración & dosificación , Flavonoides/sangre , Flavonoides/metabolismo , Glicósidos Iridoides/administración & dosificación , Glicósidos Iridoides/sangre , Glicósidos Iridoides/metabolismo , Lignanos/administración & dosificación , Lignanos/sangre , Lignanos/metabolismo , Masculino , Espectrometría de Masas/métodos , Redes y Vías Metabólicas , Ratas , Ratas Sprague-Dawley
7.
Biomed Chromatogr ; 27(11): 1503-10, 2013 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-23754598

RESUMEN

A simple and efficient liquid chromatography-mass spectrometry (LC-MS) method was developed and validated for simultaneous quantitation of catalpol and harpagide in normal and diabetic rat plasma. Protein precipitation extraction with acetonitrile was carried out using salidroside as the internal standard (IS). The LC separation was performed on an Elite C18 column (150 × 4.6 mm, 5 µm) with the mobile phase consisting of acetonitrile and water within a runtime of 12.0 min. The analytes were detected without endogenous interference in the selected ion monitoring mode with positive electrospray ionization. Calibration curves offered satisfactory linearity (r > 0.99) at linear range of 0.05-50.0 µg/mL for catalpol and 0.025-5.0 µg/mL for harpagide with the lower limits of quantitation of 0.05 and 0.025 µg/mL, respectively. Intra- and inter-day precisions (RSD) were <9.4%, and accuracy (RE) was in the -6.6 to 4.9% range. The extraction efficiencies of catalpol, harpagide and IS were all >76.5% and the matrix effects of the analytes ranged from 86.5 to 106.0%. The method was successfully applied to the pharmacokinetic study of catalpol and harpagide after oral administration of Zeng-Ye-Decoction to normal and diabetic rats, respectively.


Asunto(s)
Cromatografía Liquida/métodos , Diabetes Mellitus Experimental/tratamiento farmacológico , Hipoglucemiantes/sangre , Glucósidos Iridoides/sangre , Glicósidos Iridoides/sangre , Espectrometría de Masas/métodos , Piranos/sangre , Animales , Diabetes Mellitus Experimental/sangre , Medicamentos Herbarios Chinos/farmacocinética , Hipoglucemiantes/administración & dosificación , Glucósidos Iridoides/administración & dosificación , Glicósidos Iridoides/administración & dosificación , Límite de Detección , Masculino , Piranos/administración & dosificación , Ratas , Ratas Sprague-Dawley
8.
Pharm Biol ; 49(9): 989-93, 2011 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-21591872

RESUMEN

CONTEXT: Fructus Corni is derived from the dry ripe sarcocarp of Cornus officinalis Sieb. et Zucc. (Cornaceae). Morroniside is an active constituent of Fructus Corni used in many traditional Chinese medicines (TCMs). This article describes a sensitive and specific assay for the quantitation of morroniside in rat plasma after oral administration of iridoid glycosides from Fructus Corni. MATERIALS AND METHODS: In this article, back-propagation (BP) neural network method was fist developed for the prediction of pharmacokinetic (PK) parameters of morroniside in Fructus Corni. RESULTS: The results show that mean square error (MSE) of neural network model with 11 hidden neurons and 90% training data is 0.092. DISCUSSION AND CONCLUSION: This article provides a new method to calculate PK data, one do not need to figure out all the compartment parameters to acquire PK data of morroniside. Therefore, the BP neural network method would be useful for guiding the holistic PK study in consistence with the intrinsic theory and characteristics of TCM.


Asunto(s)
Cornus/química , Glicósidos/farmacocinética , Glicósidos Iridoides/farmacocinética , Redes Neurales de la Computación , Preparaciones de Plantas/farmacocinética , Animales , Glicósidos/administración & dosificación , Glicósidos/sangre , Glicósidos/farmacología , Glicósidos Iridoides/administración & dosificación , Glicósidos Iridoides/sangre , Glicósidos Iridoides/farmacología , Medicina Tradicional China , Fitoterapia , Preparaciones de Plantas/administración & dosificación , Preparaciones de Plantas/sangre , Preparaciones de Plantas/farmacología , Ratas
9.
Eur J Pharmacol ; 647(1-3): 68-74, 2010 Nov 25.
Artículo en Inglés | MEDLINE | ID: mdl-20826142

RESUMEN

Cornel iridoid glycoside (CIG) is a main component extracted from a traditional Chinese herb Cornus officinalis. Our previous study found that CIG improved neurological function in cerebral ischemic rats. The aim of this study was to investigate the therapeutic benefit of CIG in rats with fimbria-fornix transection (FFT) and explore the underlying molecular mechanisms. CIG (20, 60 and 180 mg/kg) or vehicle was intragastrically administered once daily to rats, starting immediately after the surgery and lasting for 4 weeks. Morris water maze and step-through tests showed that the memory deficits seen in FFT rats were significantly improved by CIG treatment. Immunohistochemical analysis showed that CIG treatment attenuated the loss of neurons in hippocampus. To elucidate the memory-improving mechanism of CIG, the neurotrophic factors, synaptic proteins and Bcl-2 family proteins in hippocampus were measured by Western blot analysis. FFT reduced hippocampal protein levels of nerve growth factor (NGF), tyrosine receptor kinase A (Trk A), brain-derived neurotrophic factor (BDNF), synaptophysin (SYP) and B-cell lymphoma-2 (Bcl-2), but not levels of tyrosine receptor kinase B (Trk B) and growth-associated protein 43 (GAP-43). FFT also elevated cytochorome C (Cyt c) and bcl-2-associated X protein (Bax). Administration of CIG to FFT rats significantly elevated the expression of NGF, TrkA, BDNF, SYP, GAP-43 and Bcl-2, and decreased the expression of Cyt c and Bax. These results indicated that CIG effectively counteracted cognitive impairments caused by fimbria-fornix lesions, and the mechanisms might be related to promoting neuronal survival and providing a beneficial environment for brain repair.


Asunto(s)
Cornus/metabolismo , Glicósidos Iridoides/farmacología , Memoria/efectos de los fármacos , Neuronas/efectos de los fármacos , Fitoterapia , Enfermedad de Alzheimer/tratamiento farmacológico , Animales , Reacción de Prevención/efectos de los fármacos , Factor Neurotrófico Derivado del Encéfalo/metabolismo , Factor Neurotrófico Derivado del Encéfalo/farmacología , Fórnix/fisiopatología , Fórnix/cirugía , Hipocampo/efectos de los fármacos , Hipocampo/metabolismo , Glicósidos Iridoides/administración & dosificación , Glicósidos Iridoides/metabolismo , Masculino , Aprendizaje por Laberinto/efectos de los fármacos , Medicina Tradicional China , Factor de Crecimiento Nervioso/metabolismo , Factor de Crecimiento Nervioso/farmacología , Factores de Crecimiento Nervioso/biosíntesis , Factores de Crecimiento Nervioso/metabolismo , Factores de Crecimiento Nervioso/farmacología , Neuronas/metabolismo , Preparaciones de Plantas/uso terapéutico , Ratas , Ratas Sprague-Dawley , Receptor trkA/metabolismo
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA