Significant Inhibition Of Paw Edema Research Articles

Phytochemistry and Therapeutic Potentials of the Seed Essential Oil of Eucalyptus maculata Hook from Nigeria

The aim of this research was to study the phytochemicals, therapeutic potentials of the seed essential oil of E. maculata Hook grown in Nigeria. Composition of the seed essential oil was investigated by GC, GC-MS, MS and FT-IR. Analyses of the volatile oil resulted in the identification of fifty-eight phytocompounds representing 98.95% of the oil. Cyclofenchene (7.0%), α-pinene (8.0%), 1R-α-pinene (6.0%), 1S-α-pinene (7.0%), DL-pinene (6.0%) and β-trans-Ocimene (8.0%) were detected as the principal components accounted for 42% of the seed essential oil. None of these main compounds has ever been detected in the leaves extracts of E. maculata that had been investigated before except α-Pinene. The total phenolics content of the seed oil of E. maculata was estimated as 195.84 ± 0.002 μg/mg GAE. The results of free radical scavenging capacity using DPPH and FRAP methods showed that the oil possessed strong antioxidant activity with IC50 8.0 and 10.0 µgml-1 respectively. The acute toxicity test showed that the seed oil extract is safe to be used in vivo. The seed oil at 1000 µgkg-1 (p.o.) gave 87.50% significant inhibition of paw edema. In the antinociceptive assay the oil inhibited the licking time by 86.46% in first phase (neurogenic pain) and 60.10% in the second phase (inflammatory pain). These results showed that the seed oil of E. maculata could be an active source of substances with antioxidant, anti-inflammatory and analgesic activities. The pharmacological potentials of the investigated seed oil could be explained by their antioxidant properties, due to their high phenolic and terpenoids contents.

The analgesic and acute anti-inflammatory effect of the ethanolic extract of the leaves of Paederia foetida (EEPF) on experimental animal models

Objective:To study the analgesic and acute anti-inflammatory effect of the ethanolic extract of the leaves of Paederia foetida (EEPF) on experimental animal models. Materials and Methods: Fresh leaves were collected, air-dried, powdered, and percolated in 95% ethanol. Acute toxicity test was done according to OECD guidelines. Healthy albino rats (150-200 gm) of either sex were taken and divided into five groups with six animals in each group for central analgesic activity by tail flick method. Peripheral analgesic activity by 1% glacial acetic acid induced writhing test by taking albino mice (20-30 gm) of either sex which were divided into three groups with six animals in each. EEPF was used in a dose of 500 mg/kg bodyweight subcutaneously for tail-flick method and orally for writhing test. In tail-flick method the basal reaction time was taken and a cut-off period of 10 sec was observed. Reaction time were recorded at predrug, 15, 30, 60, 90, 120, 150 and 180 minutes after administration of drug . The standard drug used for central analgesic activity was pethidine 5 mg/kg bw, naloxone 1mg/kg as antagonist and naloxone 1mg/kg bw with 500mg/kg bw of EEPF to study the central mechanism of action. The standard drug used for peripheral analgesic activity was aspirin 100mg/kg bw orally. A control group was maintained in all the models. For anti-inflammatory study, three groups of animals of either sex (n = 6), weighing 150-200g of the species Rattus norvegicus were taken for the study. Group A was taken as control (Normal salie, 10 mL/kg body weight), Group B as test group (EEPF 500 mg/kg body weight), and Group C as standard (Aspirin 100 mg/kg body weight). The animals were studied for acute inflammation by Carrageenan-induced rat paw edema. Statistical analysis was done by one-way analysis of variance followed by multiple comparison tests.Results: EEPF significantly increased the reaction time in tail-flick method (p<0.05) whereas the combination of naloxone and EEPF decreased the reaction time indicating that naloxone inhibits the analgesic effect of EEPF. In 1% glacial acetic acid induced writhing EEPF reduced writhing significantly In acute inflammation, there was significant inhibition of paw edema in Groups B, C in comparison with Group A (P < 0.05). Conclusion:The ethanolic extract of Paederia foetida has significant analgesic and anti-inflammatory activity. DOI: http://dx.doi.org/10.3329/bjms.v11i3.11723 Bangladesh Journal of Medical Science Vol. 11 No. 03 July’12

A study of the anti-inflammatory effect of the leaves of Psidium guajava Linn. on experimental animal models

Introduction:The aim is to study the anti-inflammatory effect of the ethanolic extract of the leaves of Psidium guajava(PGE) on experimental animal models.Materials and Methods:Fresh leaves were collected, air-dried, powdered, and percolated in 95% ethanol. Acute toxicity test was done according to OECD guidelines. Four groups of animals of either sex, weighing 150–200g of the species Rattus norvegicus were taken for the study (n = 6). Group A was taken as control (3% gum acacia in 10 mL/kg body weight), Group B as test group (PGE 250 mg/kg body weight), Group C as test group (PGE 500 mg/kg body weight), and Group D as standard (Aspirin 100 mg/kg body weight). The animals were studied for acute inflammation by Carrageenan-induced rat paw edema, subacute inflammation by Granuloma pouch method, and chronic inflammation by Freund’s adjuvant-induced arthritis method. Statistical analysis was done by one-way analysis of variance followed by multiple comparison tests.Results:In acute inflammation, there was significant inhibition of paw edema in Groups B, C, and D in comparison with Group A (P < 0.05). In subacute inflammation, there was significant inhibition of exudate formation in Groups B, C, and D in comparison to Group A (P < 0.05). In chronic inflammation, there was significant inhibition of paw edema and inhibition of weight reduction in Groups B, C, and D compared with Group A. Downregulation of arthritis index was also significant in Groups B, C, and D in comparison with Group A (P < 0.05).Conclusion:The ethanolic extract of PGE has significant anti-inflammatory activity.

Anti-inflammation activity and chemical composition of flower essential oil from Hedychium coronarium

Hedychium coronarium Koen. (Family Zingiberaceae), popularly named butterfly ginger, is widely available in tropical and subtropical regions. It has been used in folk medicine for many conditions, such as contusion inflammation, anti-rheumatic and so on. In this study, chemical compositions and anti-inflammatory activity of this flowers’ essential oil were investigated for the first time. Followed by GC–MS analysis, a total of 29 components were identified and the main constituents included
-transocimenone (28.05%), linalool (18.52%), 1,8-cineole (11.35%), -terpineol (7.11%), 10-epi--eudesmol (6.06%), sabinene (4.59%) and terpinen-4-ol (3.17%). We measured the antioxidant activity of the essential oil in vitro (DPPH reduction assay and ferric reducing antioxidant power assay) and the antiinflammatory activity in vivo (carrageenan-induced hind paw edema in rats). The oil (100 mg/kg p.o.) produced significant inhibition of paw oedema, but showed poor antioxidant activity (with the DPPH IC50 value of 1091.00
g/ml and FRAP value of 0.22
mol Fe2+/mg). The results reveal that there is no direct correlation between anti-inflammatory effect and antioxidant activity of this essential oil.

Anti-inflammatory and anti-pyretic activities of earthworm extract— Lampito mauritii (Kinberg)

Aim of the study Experiments were conducted to understand the therapeutic properties such as anti-inflammatory and anti-pyretic activities of biologically active extract isolated from whole earthworm ( Lampito mauritii, Kinberg). Materials and methods Inflammation in the hind paw of Wistar albino rat, Rattus norvegicus, was induced by histamine, granuloma pouch was induced by turpentine and pyrexia induced by Brewer's yeast in rats were followed as earlier studies. Anti-inflammatory drug—indomethacin and anti-pyretic drug—paracetamol were used as standard drug for comparison. Results Administration of indomethacin (10 mg/kg), paracetamol (150 mg/kg) and/or different doses of earthworm extract (EE) (50, 100 and 200 mg/kg) reduced and restored to normal conditions in a dose-dependent manner of histamine and turpentine induced inflammation, and Brewer's yeast induced pyretic in rats. Conclusions The most significant inhibition of paw oedema and granuloma and also the significant reduction in hyperpyrexia in rats when treated with standard drugs as well as different doses of EE, reflect the presence of anti-inflammatory and anti-pyretic properties of EE similar to glycoprotein complex (G-90).

The inhibition of paw oedema formation caused by the oil of Copaifera multijuga Hayne and its fractions

Abstract Two oils exuded from a Copaifera multijuga Hayne tree (Leguminosae-Caesalpinoideae), collected from the same plant, but in different periods of the year, and the hexanic, dichloromethanic and methanolic fractions of one of these oils were analysed by high-resolution gas chromatography (HRGC) and HRGC coupled with mass spectrometry (HRGC-MS). In addition, the in-vivo preliminary anti-oedematogenic actions of the oil and some fractions of it were assessed against carrageenan- and bradykinin-induced oedema formation in the rat paw. Twenty-seven sesquiterpenes and six diterpenes were identified, β-caryophyllene, α-copaene and copalic acid being the main components. The dichloromethanic and methanolic fractions obtained from C. multijuga oil given by the intraperitoneal route caused a significant inhibition of paw oedema caused by carrageenan with inhibition of 49 ± 13% and 64 ± 9 %, respectively. Likewise, dexamethasone (the positive control drug) also greatly inhibited carrageenan-induced paw oedema formation (60 ± 4% at 2 h). The hexanic fraction also significantly inhibited (50 ± 6%) the paw oedema formation caused by bradykinin. These results suggest the presence of still non-identified active terpene compounds in the oil of C. multijuga that exhibit anti-oedematogenic properties. Of note, the yield of these compounds and the pharmacological actions of the oil, exhibited great seasonal variations, a relevant aspect that should be carefully observed for the correct medicinal use of this plant by the population.

Relevance of tumour necrosis factor‐α for the inflammatory and nociceptive responses evoked by carrageenan in the mouse paw

1. The present study evaluated the participation of tumour necrosis factor-alpha (TNF-alpha) in the inflammatory and nociceptive responses evoked by carrageenan in the mouse paw. 2. The intraplantar injection of carrageenan (300 microg paw-1) induced a marked and biphasic paw oedema formation (peaks at 6 and 72 h), which was accompanied by a long-lasting mechanical allodynia (that remained elevated for up to 72 h) and a significant increase of myeloperoxidase (MPO) activity (peak at 6 h) in both Swiss and C57/BL6 mice. 3. The paw oedema, the elevation of MPO activity and to a lesser extent the mechanical allodynia elicited by carrageenan were found to be significantly reduced in TNF-alpha p55 receptor knockout mice. 4. Of interest, the systemic administration of an anti-TNF-alpha antibody produced a significant inhibition of paw oedema, mechanical allodynia and MPO activity. A noteworthy decrease in inflammatory and nociceptive responses caused by carrageenan was also observed when mice were previously treated with the preferential inhibitor of TNF-alpha synthesis, thalidomide. 5. The present results clearly indicate that the proinflammatory cytokine TNF-alpha plays a critical role in the oedema formation, as well as in the mechanical allodynia and the neutrophil migration, following carrageenan administration into the mouse paw. Intraplantar injection of carrageenan in mice could constitute a useful model for assessment of the in vivo effects of potential inhibitors of TNF-alpha-related pathways.

Anti-inflammatory activity of extract and fractions from Nepeta sibthorpii Bentham

Several species of Nepeta genus are utilized in folk medicine for treatment of contusions, rheumatic pains, fever, cutaneous eruptions. Some species are employed for their anti-inflammatory properties. In this paper, we report the results of phytochemical studies on aerial parts of Nepeta sibthorpii Bentham (Lamiaceae), an endemic plant of Greece. The bioassay-guided fractionation of methanol extract led to the isolation of ursolic acid and polyphenol fraction. By HPLC, we determined some phenolics: chlorogenic acid (0.315 mg/g) and the flavonoids rutin (0.091 mg/g), luteolin-7- O-glucoside (0.387 mg/g) and a luteolin derivative. We assayed the radical scavenging activity of Nepeta sibthorpii methanol extract by the 1,1-diphenyl-2-picrylhydrazyl (DPPH) method. Moreover, we studied the anti-inflammatory activity of Nepeta sibthorpii methanol extract (50 mg/kg, os), ursolic acid and polyphenol fraction (dose corresponding to 50 mg/kg of methanol extract, os) in the carrageenan-induced paw oedema in rat. In this experimental model, we observed a significant inhibition of paw oedema. We suppose that the anti-inflammatory effect of methanol extract could be related to the free radical scavenging activity and that it depends on a synergic action of all the components of the methanol extract, even if ursolic acid can be considered the main responsible for this activity.

Inflammatory effects of acute and chronic capsaicin treatment on rat paw

AbstractCapsaicin extracted from natural sources (Capsicum frutescens) and standard capsaicin (Sigma Chemicals) were used in this study. On acute treatment capsaicin produced a dose‐related inflammatory response in rat paw as measured by the volume displacement method. This response was found to be synergestic when injected with carrageenan. Preliminary experiments showed that pretreatment with diphenhydramine‐HCl produced a significant inhibition of this acute capsaicin induced paw oedema, whereas indomethacin and methysergide were ineffective in blocking paw oedema. On the other hand, chronically capsaicin treated rats (for 10 days) showed a significant inhibition of paw oedema when treated with either carregeenan or a single high dose of capsaicin. Both the extracted and the standard capsaicin showed a similar type of response in all experiments.

Effects of salmon calcitonin and combination drug therapy on rat adjuvant arthritis.

The effect of chronic administration of salmon calcitonin (SCT) to rats with adjuvant arthritis was studied. Compared to arthritic controls, 10 units/kg day in a divided dose of SCT given s.c. resulted in a significant inhibition of paw edema and a reduction in the marked deterioration of the bones of the hind limbs, particularly those of the tarsus, as visualized by x-ray. In addition, a pronounced increase in bone density in the proximal metaphyseal area of the tibia was consistently observed in calcitonin treated animals. Animals treated with SCT also showed improved clinical symptoms including increased mobility and decreased sensitivity to handling compared to arthritic controls.