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1.
Article in English | MEDLINE | ID: mdl-17923400

ABSTRACT

Ginger, the rhizome of Zingiber officinalis Roscoe (Zingiberaceae), is a common constituent of diets around the world and its extracts have been reported to exhibit several pharmacological activities. We investigated the effect of crude hydroalcoholic extract of ginger on the rat trachea hyperreactivity (RTHR) and lung inflammation induced by lipopolysaccharide (LPS). Our results demonstrate that ginger extract and celecoxib attenuated RTHR 90 min and 48 h after LPS. Ginger and celecoxib reduced the serum level of prostaglandin (PGE2) and thromboxane (TXA2) 90 min after LPS. Celecoxib and ginger also reduced myeloperoxidase activity and the number of cells in rat bronchoalveolar lavage 48 h post-LPS. On lung parenchyma, ginger and celecoxib reduced the release of PGE2 and TXA2 48 h post-LPS. These results suggest that ginger exerts an anti-inflammatory effect on lung attenuating RTHR and COX metabolites seem to be involved in these processes.


Subject(s)
Bronchial Hyperreactivity/drug therapy , Plant Extracts/therapeutic use , Pneumonia/drug therapy , Trachea/physiopathology , Zingiber officinale/chemistry , Animals , Bronchial Hyperreactivity/chemically induced , Bronchoalveolar Lavage Fluid/cytology , Celecoxib , Dinoprostone/blood , Lipopolysaccharides , Male , Masoprocol/pharmacology , Phytotherapy , Pneumonia/chemically induced , Pyrazoles/pharmacology , Rats , Rats, Wistar , Rhizome/chemistry , Sulfonamides/pharmacology , Thromboxane A2/blood , Trachea/drug effects
2.
Phytomedicine ; 10(5): 381-5, 2003.
Article in English | MEDLINE | ID: mdl-12834002

ABSTRACT

Plant extracts have been used for centuries as a popular mode of treatment for several health disorders. Over the last ten years, the study of those extracts has attracted attention in different fields of the biological sciences. Ginger, the rhizome of Zingiber officinale Roscoe (Zingiberaceae), is a commom constituent of diet worldwide and it has been reported that its extracts present some pharmacological activities. Here we investigate the effects of the crude hydralcoholic extract of ginger rhizomes on the classical models of rat paw and skin edema. The carrageenan-, compound 48/80- or serotonin-induced rat paw edema were inhibited significantly by the intraperitoneal administration of alcoholic ginger extract. Ginger extract was also effective in inhibiting 48/80-induced rat skin edema at doses of 0.6 and 1.8 mg/site. Rat skin edema induced by substance P or bradikinin was not affected by treatment with Z. officinalle extract. The intraperitoneal administration of ginger extract (186 mg/kg(-1) body wt.) 1 h prior to serotonin injections, reduced significantly the serotonin-induced rat skin edema. Our results demonstrated that crude extract of Zingiber officinale was able to reduce rat paw and skin edema induced by carrageenan, 48/80 compound and serotonin. The antiedematogenic activity seems to be related, at least partially, to an antagonism of the serotonin receptor.


Subject(s)
Anti-Inflammatory Agents/pharmacology , Edema/drug therapy , Plant Extracts/pharmacology , Rhizome/chemistry , Zingiber officinale/chemistry , Animals , Anti-Inflammatory Agents/chemistry , Anti-Inflammatory Agents/therapeutic use , Edema/chemically induced , Male , Plant Extracts/chemistry , Plants, Medicinal/chemistry , Rats , Rats, Wistar , Serotonin/pharmacology , Skin/drug effects , Skin/pathology , p-Methoxy-N-methylphenethylamine/pharmacology
3.
Phytomedicine ; 9(3): 245-8, 2002 Apr.
Article in English | MEDLINE | ID: mdl-12046866

ABSTRACT

Petiveria alliacea L (Phytolaccaceae) is a perennial bush plant that grows widely in Brazil. The roots and leaves of P. alliacea have been used in folk medicine for their antispasmodic, sedative, diuretic and antihelminthic actions. We recently described the anti-inflammatory properties of P. alliacea administered topically and orally in different animal models. In the present study, we investigated the anti-inflammatory activity of a crude lyophilized extract of P. alliacea roots administered to rats with pleurisy. The oral administration of P. alliacea root extract did not significantly reduce the total number of leukocytes at the doses tested. By contrast, the highest dose of extract tested (43.9 mg/kg body wt.) significantly reduced the number of migrating neutrophils, mononuclear cells and eosinophils; the dose of 31.4 mg/kg body wt. also reduced mononuclear cell migration. The P. alliacea root extract also showed a significant analgesic effect in the experimental model used. The results of this study provide a basis for the use of P. alliacea extracts in popular folk medicine, but further studies are necessary to elucidate the mechanism of its anti-inflammatory and analgesic actions.


Subject(s)
Analgesics/pharmacology , Anti-Inflammatory Agents/pharmacology , Leukocytes/drug effects , Pain/drug therapy , Phytolaccaceae , Phytotherapy , Plant Extracts/pharmacology , Pleurisy/drug therapy , Administration, Oral , Analgesics/administration & dosage , Analgesics/therapeutic use , Animals , Anti-Inflammatory Agents/administration & dosage , Anti-Inflammatory Agents/therapeutic use , Carrageenan , Disease Models, Animal , Dose-Response Relationship, Drug , Leukocytes/physiology , Male , Pain/chemically induced , Plant Extracts/administration & dosage , Plant Extracts/therapeutic use , Plant Leaves , Plant Roots , Pleurisy/chemically induced , Rats , Rats, Wistar
4.
J Ethnopharmacol ; 31(2): 239-47, 1991 Feb.
Article in English | MEDLINE | ID: mdl-2023431

ABSTRACT

The antiinflammatory effects and gastrotoxicity of a lyophilized 70% ethanol extract of the leaves of Cordia verbenacea were investigated through experimental models in rats and mice. The oral administration of 1.24 mg/kg of the extract significantly inhibited nystatin-induced oedema. Topical application of the extract at a dose of 0.09 mg/ear in mice was clearly more effective than 1.0 mg/ear of naproxen in the reduction of the ear oedema induced by corton oil. At antiinflammatory doses, the extract showed an important protective effect on the gastric mucosa, reducing significantly the number of gastric lesions.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/isolation & purification , Plants, Medicinal , Animals , Anti-Inflammatory Agents, Non-Steroidal/administration & dosage , Anti-Inflammatory Agents, Non-Steroidal/toxicity , Dermatitis/drug therapy , Edema/drug therapy , Gastric Mucosa/drug effects , Male , Mice , Plant Extracts/administration & dosage , Plant Extracts/isolation & purification , Plant Extracts/toxicity , Rats , Rats, Inbred Strains
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