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1.
Indian J Exp Biol ; 52(8): 808-13, 2014 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-25141544

RESUMEN

Guduchi has been widely used in the traditional medicine as an immunomodulator. Description of guduchi in Ayurvedic literature resemble with T. sinensis rather than with commonly available T. cordifolia and hence this may be used as substitutes for T. sinensis. T. cordifolia growing on Azadirachta indica commonly called Neem-guduchi has more immunomodulatory potential. Thus, immunomodulatory activity of three Tinospora spp. was assessed by checking humoral and cell mediated immune responses to the antigenic challenges with sheep RBCs and by neutrophil adhesion tests on albino Wistar rats using Guduchi-Satwa, a well known dosage form. Results revealed that Neem-guduchi possesses higher immunomodulatory potential at the dose of 300 mg/kg, po and validated the traditional claim. Hence, Neem-Guduchi can be employed in immunomodulatory formulation prepared using guduchi.


Asunto(s)
Inmunomodulación , Extractos Vegetales/administración & dosificación , Tinospora/inmunología , Animales , Azadirachta/química , Azadirachta/crecimiento & desarrollo , Neutrófilos/efectos de los fármacos , Neutrófilos/inmunología , Fagocitosis/efectos de los fármacos , Fagocitosis/inmunología , Extractos Vegetales/química , Extractos Vegetales/inmunología , Ratas , Tinospora/química
2.
Trop Anim Health Prod ; 42(4): 645-51, 2010 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-19876755

RESUMEN

Enhancement of the diseased mammary gland immunity and therapeutic potential of hydro-methanolic extract of Tinospora cordifolia (T. cordifolia; stem) in bovine subclinical mastitis was investigated. Somatic cell count (SCC), total bacterial count (TBC), phagocytic activity, and leukocyte lysosomal enzymes like myeloperoxidase and acid phosphatase activity and Interleukin-8 (IL-8) level were evaluated after intramammary infusion of hydro-methanolic extract (stem) of T.cordifolia in diseased cows. The qualitative analysis of the extract revealed the presence of polysaccharide, phenol, alkaloid, and protein. Intramammary infusion of hydro-methanolic extract of T. cordifolia treatment initially enhanced the SCC; thereafter, significant reduction in cell count (P < 0.05) was observed on day 15 of the treatment period, however, reduction in TBC was observed from day 3 onwards. The phagocytic activity of milk polymorphonuclear cells enhanced in the diseased cows treated with the T. cordifolia extract. Similarly, the lysosomal enzyme content of the milk polymorphonuclear cells enhanced significantly (P < 0.05) in diseased cows treated with T. cordifolia. The IL-8 level in milk serum also increased significantly (P < 0.05) in diseased cows treated with the herb extract. The results suggest that the hydro-methanolic extract of T.cordifolia (stem) possesses antibacterial and immunomodulatory properties. In the present study, the biological activity of the Tinospora cordifolia extract at standardized dose against bovine subclinical mastitis is reported for the first time. Development of alternative therapy with medicinal plants is an option for livestock farmers who are not allowed to use the conventional allopathic drugs under certain farming system or cannot afford to use allopathic drugs.


Asunto(s)
Mastitis Bovina/tratamiento farmacológico , Mastitis Bovina/inmunología , Fitoterapia/métodos , Extractos Vegetales/uso terapéutico , Tinospora/química , Fosfatasa Ácida/análisis , Animales , Bovinos , Recuento de Células/veterinaria , Femenino , Interleucina-8/análisis , Mastitis Bovina/microbiología , Leche/citología , Leche/enzimología , Leche/microbiología , Muramidasa/análisis , Neutrófilos/citología , Neutrófilos/inmunología , Neutrófilos/microbiología , Peroxidasa/análisis , Fagocitosis , Tallos de la Planta/química , Tinospora/inmunología
3.
Indian J Med Sci ; 61(6): 347-55, 2007 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-17558098

RESUMEN

BACKGROUND: Chronic diabetic patients with wounds have deficient growth factors and impaired local and systemic cellular immunity. Treatment with growth factors is expensive with risk of infection transmission and these factors may not achieve optimum wound concentration. We evaluated the role of generalized immunomodulation in diabetic ulcers by using Tinospora cordifolia as an adjuvant therapy and studied its influence on parameters/determinants of healing, on bacterial eradication and on polymorphonuclear phagocytosis. MATERIALS AND METHODS: A prospective double-blind randomized controlled study lasting for over 18 months in 50 patients. The ulcer was classified by wound morphology and severity with Wound Severity Score (Pecoraro-Reiber system). Mean ulcer area, depth and perimeter were measured and swabs taken for culture. Blood was collected to assess polymorphonuclear % phagocytosis (PMN function by Lehrer-Cline C. albicans method). Medical therapy, glycemic control, debridement, wound care were optimized. At 4 weeks, parameters were reassessed. PMN function was reviewed at 3 months. RESULTS AND ANALYSIS: Forty-five patients completed the trial: study group - 23 (M:F = 17:1; mean age = 56.3 years; mean ulcer duration = 21.1 days); control group 22 (M:F = 19:3; mean age = 56.3 years; mean ulcer duration = 30.4 days). Net improvement was seen in 17 patients (73.9%) in the study group; while in the control group, in 13 patients (59.1%); P = 0.292. Specific parameters included rate of change of ulcer area - cm(2) /day (study - 0.15; control - 0.07; P = 0.145); rate of change of ulcer perimeter - mm/day (study - 0.09; control = - 0.07; P = 0.089); change of depth - mm (study - 2.2; control - 1.4; P = 0.096); change of wound score (study - 14.4; control - 10.6; P = 0.149); total number of debridements (study - 1.9; control - 2.5; P = 0.03) and change in % phagocytosis (study - 3.9; control - 2.3; P = 0.048). CONCLUSION: Diabetic patients with foot ulcers on T. cordifolia as an adjuvant therapy showed significantly better final outcome with improvement in wound healing. Reduced debridements and improved phagocytosis were statistically significant, indicating beneficial effects of immunomodulation for ulcer healing.


Asunto(s)
Pie Diabético/tratamiento farmacológico , Úlcera del Pie/tratamiento farmacológico , Fitoterapia/métodos , Tinospora/inmunología , Cicatrización de Heridas/efectos de los fármacos , Inductores de la Angiogénesis/economía , Inductores de la Angiogénesis/uso terapéutico , Becaplermina , Pie Diabético/inmunología , Pie Diabético/cirugía , Método Doble Ciego , Femenino , Úlcera del Pie/inmunología , Úlcera del Pie/cirugía , Humanos , Masculino , Neutrófilos/efectos de los fármacos , Preparaciones de Plantas/uso terapéutico , Factor de Crecimiento Derivado de Plaquetas/economía , Factor de Crecimiento Derivado de Plaquetas/uso terapéutico , Estudios Prospectivos , Proteínas Proto-Oncogénicas c-sis , Proteínas Recombinantes , Cicatrización de Heridas/inmunología
4.
Int Immunopharmacol ; 50: 168-177, 2017 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-28667885

RESUMEN

Macrophages are centrally placed in the innate immune system and their activation is crucial to the generation of appropriate immune response in the event of any pathogenic invasion, tumorigenesis or other human diseases. Many plant derived polysaccharides are known to activate macrophages. In the present study, effects of G1-4A, a polysaccharide derived from Tinospora cordifolia, on the activation of macrophages were investigated. Our data demonstrated the up regulation of expression of TNF-α, IL-ß, IL-6, IL-12, IL-10 and IFN-γ in RAW 264.7 cell line and peritoneal macrophages after G-14A treatment. Nitric oxide levels were also enhanced along with up-regulation of NOS2 expression in murine macrophages post G1-4A treatment. Further, G1-4A treatment up-regulated the surface expression of MHC-II and CD-86 in macrophages. Using siRNA against TLR4, MyD88 and anti-TLR4 blocking antibodies, we established that G1-4A activated macrophages by classical pathway in TLR4-MyD88 dependent manner. Additionally, G1-4A treatment activated p38, ERK and JNK MAPKs in macrophages. Using pharmaceutical inhibitors of above MAPKs we concluded that G1-4A activates the macrophages by activation of p38, ERK and JNK MAPKs in RAW264.7 macrophages. Thus our data suggests the activation of macrophages by classical pathway after treatment of G1-4A.


Asunto(s)
Adyuvantes Inmunológicos , Macrófagos/inmunología , Factor 88 de Diferenciación Mieloide/metabolismo , Polisacáridos/inmunología , Receptor Toll-Like 4/metabolismo , Animales , Anticuerpos Bloqueadores/metabolismo , Citocinas/metabolismo , Femenino , Inmunidad Innata , Mediadores de Inflamación/metabolismo , Sistema de Señalización de MAP Quinasas , Activación de Macrófagos , Ratones , Ratones Endogámicos BALB C , Factor 88 de Diferenciación Mieloide/genética , Óxido Nítrico Sintasa de Tipo II/genética , Óxido Nítrico Sintasa de Tipo II/metabolismo , Células RAW 264.7 , ARN Interferente Pequeño/genética , Transducción de Señal , Tinospora/inmunología , Receptor Toll-Like 4/genética
5.
J Immunol Res ; 2017: 1787803, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-29318160

RESUMEN

The present study was aimed at determining the activity of aqueous and methanolic extracts of Tinospora cordifolia (AETC and METC) against Salmonella typhimurium. In vitro anti-Salmonella activity of T. cordifolia was determined through the broth dilution and agar well diffusion assays. The immune-stimulating potential of AETC or METC was determined by measuring the cytokine levels in the culture supernatants of treated murine J774 macrophages. Antibacterial activity of AETC or METC was determined by treating S. typhimurium-infected macrophages and BALB/C mice. The toxicity of AETC or METC was determined by measuring the levels of liver inflammation markers aspartate transaminase (AST) and alanine transaminase (ALT) and antioxidant enzymes. Macrophages treated with AETC or METC secreted greater levels of IFN-γ, TNF-α, and IL-1ß. METC showed greater activity against S. typhimurium infection in macrophages and mice as well. Treatment with METC resulted in increased survival and reduced bacterial load in S. typhimurium-infected mice. Moreover, METC or AETC treatment reduced the liver inflammation and rescued the levels of antioxidant enzymes in S. typhimurium-infected mice. The results of the present study suggest that the use of T. cordifolia may act as a double-edged sword in combating salmonellosis.


Asunto(s)
Hepatitis A/terapia , Macrófagos/efectos de los fármacos , Extractos Vegetales/uso terapéutico , Salmonelosis Animal/terapia , Infecciones por Salmonella/terapia , Salmonella typhimurium/fisiología , Alanina Transaminasa/sangre , Animales , Aspartato Aminotransferasas/sangre , Carga Bacteriana/efectos de los fármacos , Línea Celular , Citocinas/metabolismo , Hepatitis A/inmunología , Humanos , Inmunomodulación , Mediadores de Inflamación/metabolismo , Macrófagos/inmunología , Macrófagos/microbiología , Metanol/química , Ratones , Ratones Endogámicos BALB C , Infecciones por Salmonella/inmunología , Salmonelosis Animal/inmunología , Salmonella typhimurium/efectos de los fármacos , Tinospora/inmunología , Agua/química
6.
Int Immunopharmacol ; 4(13): 1569-75, 2004 Dec 15.
Artículo en Inglés | MEDLINE | ID: mdl-15454110

RESUMEN

The antiangiogenic activity of Tinospora cordifolia was studied using in vivo as well as in vitro models. In vivo antiangiogenic activity was studied using B16F10 melanoma cell-induced capillary formation in animals. Intraperitoneal administration of the extract at a concentration of 20 mg/kg significantly inhibited the tumour directed capillary formation induced by melanoma cells. Analysis of the serum cytokine profile showed a drastic increase of proinflammatory cytokines such as IL-1beta, IL-6, TNF-alpha, granulocyte monocyte-colony stimulating factor (GM-CSF) and the direct endothelial cell proliferating agent vascular endothelial cell growth factor (VEGF) in the angiogenesis-induced control animals. Administration of Tinospora extract could differentially regulate these cytokine's elevation. The differential regulation is further evidenced by the increased production of antiangiogenic agents IL-2 and tissue inhibitor of metalloprotease-1 (TIMP-1) in the B16F10-injected, extract-treated animals. Moreover, using an in vitro rat aortic ring assay, it was observed that the extract at nontoxic concentrations inhibited the production of proangiogenic factors from B16F10 melanoma cells. Direct treatment of the extract also inhibits the microvessel outgrowth from the aortic ring. Hence, the observed antiangiogenic activity of the plant T. cordifolia is related, at least in part, to the regulation of the levels of these cytokines and growth factors in the blood of the angiogenesis-induced animal.


Asunto(s)
Citocinas/efectos de los fármacos , Neovascularización Patológica/prevención & control , Tinospora/química , Inhibidores de la Angiogénesis/inmunología , Inhibidores de la Angiogénesis/farmacología , Animales , Aorta/patología , Línea Celular Tumoral , Citocinas/sangre , Modelos Animales de Enfermedad , Ensayos de Selección de Medicamentos Antitumorales/métodos , Factor Estimulante de Colonias de Granulocitos y Macrófagos/sangre , Factor Estimulante de Colonias de Granulocitos y Macrófagos/efectos de los fármacos , Factor Estimulante de Colonias de Granulocitos y Macrófagos/inmunología , Inyecciones Intraperitoneales , Masculino , Melanoma Experimental/inmunología , Melanoma Experimental/patología , Ratones , Ratones Endogámicos C57BL , Neovascularización Patológica/fisiopatología , Extractos Vegetales/inmunología , Extractos Vegetales/aislamiento & purificación , Extractos Vegetales/farmacología , Tallos de la Planta/química , Ratas , Ratas Sprague-Dawley , Tinospora/inmunología , Inhibidor Tisular de Metaloproteinasa-1/sangre , Inhibidor Tisular de Metaloproteinasa-1/efectos de los fármacos , Inhibidor Tisular de Metaloproteinasa-1/inmunología , Células Tumorales Cultivadas/efectos de los fármacos , Células Tumorales Cultivadas/inmunología , Factor A de Crecimiento Endotelial Vascular/sangre , Factor A de Crecimiento Endotelial Vascular/efectos de los fármacos , Factor A de Crecimiento Endotelial Vascular/inmunología
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