scholarly journals Analgesic and Anti-Inflammatory Activities of Sophocarpine from Sophora viciifolia Hance

2021 ◽  
Vol 2021 ◽  
pp. 1-7
Author(s):  
F. L. Wang ◽  
H. Wang ◽  
J. H. Wang ◽  
D. X. Wang ◽  
Y. Gao ◽  
...  
Keyword(s):  
Acetic Acid ◽  
Total Duration ◽  
Inflammatory Factors ◽  
Tail Flick ◽  
Edible Plant ◽  
Hot Plate ◽  
Dependent Inhibition ◽  
Dose Dependent Inhibition ◽  
Anti Inflammatory ◽  
Dose Dependent

Sophora viciifolia Hance is an edible plant used in traditional Chinese medicine. Sophocarpine, a tetracyclic quinolizidine alkaloid, is one of the most abundant active ingredients in Sophora viciifolia Hance. Here, we study the analgesic and anti-inflammatory effects, as well as the acute toxicity of sophocarpine from Sophora viciifolia Hance in mice. Sophocarpine (20, 40, and 80 mg/kgbw) significantly prolonged the delay period before a hot plate reaction occurred (all P < 0.05 ), and the delay before a tail-flick response was induced by a warm bath ( P < 0.05 ; P < 0.01 ). Sophocarpine (40, 80 mg/kg) resulted in dose-dependent inhibition of the writhing reaction induced by acetic acid in mice ( P < 0.05 ; P < 0.001 , respectively). Sophocarpine (80 mg/kg) reduced the total duration of a formalin-induced pain response ( P < 0.05 ). Sophocarpine prolonged the foot-licking latency of mice after the hot plate reaction, and this effect was antagonized by calcium chloride and enhanced by verapamil. Sophocarpine (20, 40, and 80 mg/kg) significantly inhibited xylene-induced ear edema ( P < 0.01 ; P < 0.001 ; P < 0.001 , respectively) and the penetration of acetic acid-induced dye into the peritoneal cavity ( P < 0.01 ; P < 0.01 ; P < 0.001 , respectively). It also reduced the levels of proinflammatory cytokine interleukin (IL)-1β, IL-6, and prostaglandin E2 ( P < 0.05 , P < 0.01 , P < 0.001 ) and those of serum nitric oxide ( P < 0.05 ). The results of this study suggest that sophocarpine possesses certain analgesic and anti-inflammatory activities, which may be related to calcium and inhibition of the secretion of inflammatory factors.

scholarly journals Evaluation on Analgesic and Anti-Inflammatory Activities of Total Flavonoids from Juniperus sabina

2018 ◽  
Vol 2018 ◽  
pp. 1-9 ◽  
Author(s):  
Jun Zhao ◽  
Aosimanjiang Maitituersun ◽  
Chenyang Li ◽  
Qian Li ◽  
Fang Xu ◽  
...  
Keyword(s):  
Acetic Acid ◽  
Total Flavonoids ◽  
Hot Plate ◽  
Egg Albumin ◽  
Inhibition Ratio ◽  
Paw Oedema ◽  
Dependent Inhibition ◽  
Anti Inflammatory ◽  
Juniperus Sabina ◽  
Dose Dependent

The leaves of Juniperus sabina (Cupressaceae) are used in traditional Uygur medicine for the treatment of rheumatism and arthritic pain. This study aimed to investigate the analgesic and anti-inflammatory effects of total flavonoids from leaves of Juniperus sabina (JSTF) on rodents. The anti-inflammatory activity was investigated using the carrageenan, egg albumin, or histamine-induced rat paw edema as well as xylene-induced ear edema, capillary permeability, and cotton pellet granuloma while the antinociceptive activity was evaluated using the mouse writhing, formalin, and hot-plate tests. JSTF (125, 250, 500 mg/kg) significantly inhibited xylene-induced ear edema in mice (inhibition ratio as 16.22%, 40.67%, and 51.78%, respectively) and also significantly ameliorated acetic acid increased vascular permeability in mice (inhibition ratio as 11.63%, 32.56%, and 53.49%, respectively). JSTF (250 and 500 mg/kg) gave significant reduction of carrageenin-induced paw oedema at the interval of 1 h and 5 h. Administration of JSTF (500 mg/kg) caused a significant anti-inflammatory effect against oedema induced by egg albumin or histamine at the interval of 0.5 h and 4 h, and both which induced the paw oedema were also inhibited by JSTF (250 mg/kg) at a point in 1, 2, or 3 h after the inflammation. Furthermore, JSTF (125, 250, and 500 mg/kg) produced time-course increase in pain threshold in hot-plate test also. JSTF produced concentration-dependent inhibition on cyclooxygenase-2 (COX-2) or 5-lipoxygenase (5-LO) activities in vitro, and their IC50 values were 31.92 and 129.26 μg/mL, respectively. Moreover, JSTF significantly caused a significant dose-dependent inhibition on acetic acid induced writhing response in mice (inhibition ratio as 23.27%, 36.91%, and 50.76%, respectively). JSTF also significantly ameliorated formalin-induced pain in mice in the late phase on dose-dependent way. These results confirms the clinical use of J. sabina for treatment of rheumatoid arthritis in ethnomedicine, and its effective mechanism will be further studied in the future.

scholarly journals Preliminary assessment of the anti-inflammatory and analgesic effects of methanol leaf extract of Cussonia barteri (Araliaceae) in rodents

2019 ◽  
Vol 65 (3) ◽  
pp. 22-31
Author(s):  
Ighodaro Igbe ◽  
Osaze Edosuyi ◽  
Agbonlahor Okhuarobo ◽  
Adarki Pongri ◽  
Nkechi Maduako ◽  
...  
Keyword(s):  
Acetic Acid ◽  
Analgesic Effect ◽  
Leaf Extract ◽  
Methanol Extract ◽  
Tail Flick ◽  
Hot Plate ◽  
Analgesic Effects ◽  
Paw Oedema ◽  
Anti Inflammatory ◽  
Ear Oedema

Summary Introduction: Potato (Solanum tuberosum L.) is an important vegetable crop in Syria. Potato tuber moth Cussonia barteri is a small tree that grows in the sub-Saharan part of Africa. Various parts of the plant are used for the treatment of a variety of ailments in ethno-medicine. Objective: To evaluate the anti-inflammatory and analgesic effect of the methanol leaf extract of Cussonia barteri. Material and methods: The leaves were air-dried, powdered and repeatedly extracted with methanol using a Soxhlet apparatus. The resulting methanol extract (100, 200 and 400 mg/kg) was evaluated for anti-inflammatory activity using carrageenan-induced paw oedema, xylene-induced ear oedema and formalin-induced arthritis tests. Analgesic effect was evaluated using acetic acid-induced mouse writhing, hot plate and tail flick tests. Results: All doses of the extract significantly (p<0.05) reduced carrageenan-induced paw oedema, however the 400 mg/kg dose gave a sustained effect. The extract significantly inhibited xylene induced ear oedema at all doses. There were no significant (p>0.05) reductions in paw swellings due to formalin. In the acetic acid induced writhing test, the extract significantly (p<0.05) decreased writhing at 400 mg/kg only. Reaction times were not significantly different from the control in the hot plate and tail flick tests. Conclusion: This study has shown that the methanol extract possesses acute anti-inflammatory and peripherally mediated analgesic effects.

scholarly journals The Anti-Nociceptive Potential of Tulathromycin against Chemically and Thermally Induced Pain in Mice

Pharmaceutics ◽  
2021 ◽  
Vol 13 (8) ◽  
pp. 1247
Author(s):  
Mohamed Elbadawy ◽  
Amira Abugomaa ◽  
Hussein M. El-Husseiny ◽  
Ahmed S. Mandour ◽  
Mohamed M. Abdel-Daim ◽  
...  
Keyword(s):  
Acetic Acid ◽  
Acute Pain ◽  
Symptomatic Relief ◽  
Late Phase ◽  
Control Group ◽  
Tail Flick ◽  
Nociceptive Response ◽  
Hot Plate ◽  
Significant Prolongation ◽  
Dose Dependent

The present study was conducted to evaluate the analgesic potential of the new triamilide macrolide antibiotic, tulathromycin, at 20 and 40 mg/kg of body weight (BW), subcutaneously against acute pain in mice. Acute pain was induced either chemically (using acetic acid-induced writhing and formalin-induced pain tests) or thermally (using hot-plate, and tail-flick tests). In the acetic acid-induced writhing test, tulathromycin induced a dose-dependent and significant decrease in the number of writhes compared with the control group. In the late phase of the formalin test, a significant decline in hind paw licking time compared with the control group was observed. In the hot-plate and tail-flick tests, tulathromycin caused a dose-dependent and significant prolongation of latency of nociceptive response to heat stimuli, compared with the control group. These findings may indicate that tulathromycin possesses significant peripheral and central analgesic potentials that may be valuable in symptomatic relief of pain, in addition to its well-established antibacterial effect.

scholarly journals Evaluation of analgesic and anti-inflammatory activity of a combination of tramadol-pregabalin in animal models of pain and inflammation

2017 ◽  
Vol 6 (6) ◽  
pp. 1511
Author(s):  
Suthakaran C. ◽  
Raja T. A. R. ◽  
Kayalvizhi M. K. ◽  
Nithya K. ◽  
Ramnarayana Reddy R. V.
Keyword(s):  
Acetic Acid ◽  
Reaction Time ◽  
Animal Models ◽  
Inflammatory Activity ◽  
Tail Flick ◽  
High Dose ◽  
Hot Plate ◽  
Provide Pain Relief ◽  
Anti Inflammatory ◽  
Rats And Mice

Background: A major goal of pain management is to provide pain relief that is clinically meaningful, sustained, and associated with minimum and reversible adverse effects. Since single analgesic drug is not effective in all patients, there is a need either to develop new and more effective drugs or to identify favourable combinations of drugs that are already available. The aim of the present was to evaluate the analgesic and anti-inflammatory activity of tramadol and pregabalin when used alone or in combination in animal models of pain and inflammation.Methods: The animals (rats and mice) were divided into eight groups with six animals in each group. Analgesia was assessed by acetic acid induced writhing and tail flick methods in mice and hot plate method in rats. Paw oedema model in rats after induction with 0.1 ml of 1% carrageenan was used to assess the anti‑inflammatory activity. The percentage inhibition of writhes and prolongation of reaction time were used for assessing analgesic activity and reduction in paw volume was used for assessing anti-inflammatory activity. The results obtained were analysed by ANOVA and Tukey HSD Post-hoc Test.Results: Treatment with tramadol pregabalin alone or in combination reduced writhing episodes significantly in acetic acid induced writhing in mice as compared to control indicating its analgesic effect and the highest percentage inhibition of pain was seen with high dose tramadol plus pregabalin. Treatment in Hot plate and Tail flick methods significantly prolonged the reaction time at all time points.Conclusions: Tramadol when combined with pregabalin may enhance its anti-nociceptive effects. If confirmed in additional models of acute and/or chronic pain this combination might be useful in the clinical management of pain not associated with inflammation.

Anti-nociceptive activity of a few structurally related trimethoxy flavones and possible mechanisms involved

2016 ◽  
Vol 27 (2) ◽  
Author(s):  
Jagan Nadipelly ◽  
Vijaykumar Sayeli ◽  
Parimala Kadhirvelu ◽  
Jaikumar Shanmugasundaram ◽  
Binoy Varghese Cheriyan ◽  
...  
Keyword(s):  
Acetic Acid ◽  
Hot Water ◽  
Dependent Manner ◽  
Tail Immersion ◽  
Dopaminergic Mechanisms ◽  
Dependent Inhibition ◽  
Dose Dependent Inhibition ◽  
Dose Dependent ◽  
Definite Role

AbstractThe present study was designed to investigate the anti-nociceptive activity of a few structurally related trimethoxy flavones (7,2′,3′-TMF, 7,2′,4′-TMF, 7,3′,4′-TMF and 7,5,4′-TMF) and the possible mechanisms involved.Anti-nociceptive activity was evaluated in mice by employing acetic acid-induced writhing, formalin-induced nociception and hot water tail immersion methods. The involvement of opioid, GABAergic, tryptaminergic, adrenergic and dopaminergic mechanisms and KTrimethoxy flavones exhibited a significant and dose-dependent inhibition of acetic acid writhing. The paw-licking response time was reduced both in the early and late phases of formalin nociception in a dose-dependent manner by trimethoxy flavones. A significant increase in tail withdrawal latency time was also observed after trimethoxy flavones treatment. These observations revealed the potential anti-nociceptive action of the investigated trimethoxy flavones. Pretreatment with naloxone and bicuculline significantly attenuated the reduction of abdominal constrictions produced by all the tested trimethoxy flavones indicating a definite role of opioid and GABAergic mechanisms in the anti-nociceptive effect of trimethoxy flavones. The anti-nociceptive action elicited by various trimethoxy flavones was differently modulated by glibenclamide, ondansetron, yohimbine and sulpiride.The investigated trimethoxy flavones exhibited promising anti-nociceptive activity in various nociceptive models, and multiple mechanisms are involved in the anti-nociceptive activity of these compounds.

scholarly journals Pharmacological Potential of Anti-Inflammatory and Anti Nociceptive Activity of Bioactive Fractions from Leaves of Maytenus emarginata

2021 ◽  
Vol 71 (1) ◽  
Author(s):  
Sunil Kumar ◽  
Mathew George ◽  
Lincy Joseph
Keyword(s):  
Cardiac Glycosides ◽  
Methyl Cellulose ◽  
Dependent Manner ◽  
Dependent Inhibition ◽  
Pure Compounds ◽  
Cotton Pellet Granuloma ◽  
Dose Dependent Inhibition ◽  
Anti Inflammatory ◽  
Pharmacological Potential ◽  
Dose Dependent

The antinociceptive & anti-inflammatory activities of extract were compared to dose of Phenylbutazone. The phytochemical secondary metabolites tested for include alkaloids, cardiac glycosides, flavonoids, phenols, saponins, steroids and terpenoids. Maytenus emarginata leaves extract demonstrated significant antinociceptive and anti- inflammatory effects in a dose-dependent manner. The extract dose at 200mg/kg bw exhibited the highest antinociceptive and anti-inflammatory activities & its activities were comparable to those of the respective reference drugs. BFLME (suspended in 1% carboxy methyl cellulose) in doses of 50, 100 and 200 mg/kg caused a dose-dependent inhibition of swelling caused by carrageenin equivalent to 30.2–63.2% protection (P<0.05– P<0.001) and in cotton pellet granuloma, 47.2–45.4% protection (P<0.01-P<0.001) was observed from inflammation. There was a significant increase in analgesiometer force induced pain in rat equivalent to 98.1–146.5% protection (P<0.01-P<0.001) and 7.19–37.8 % (P<0.05–P<0.001) protection against Acetic acid induced writhing. Phytochemical screening of the extract indicated the presence of alkaloids, cardiac glycosides, flavonoids, phenols, saponins, steroids and terpenoids. The present study therefore demonstrated the antinociceptive and anti-inflammatory properties of bioactive fraction of ethyl acetate extract from leaves of M. emarginata (BFLME), hence providing a basis for further research that may result in pure compounds that can be advanced into drug discovery.

scholarly journals Antinociceptive and anti-inflammatory effects of Lantana camara L. extract in mice

2015 ◽  
Vol 17 (2) ◽  
pp. 224-229 ◽  
Author(s):  
T.S.C. SILVA ◽  
I.B. SUFFREDINI ◽  
E.L. RICCI ◽  
S.R.C. FERNANDES ◽  
V.JR GONÇALVES ◽  
...  
Keyword(s):  
Acetic Acid ◽  
Analgesic Activity ◽  
Lantana Camara ◽  
Tail Flick ◽  
Male Mice ◽  
Paw Edema ◽  
Hot Plate ◽  
Active Compounds ◽  
The Family ◽  
Anti Inflammatory

ABSTRACT:he Lantana camara L. belongs to the family Verbenaceae, which contains several active compounds in leaves and roots and which are reported to have medicinal and insecticidal properties. Studies of plants within the same family show the existence of anti-inflammatory activity in paw edema induced by carrageenan, serotonin and histamine and analgesic activity in the acetic acid writhing and tail-flick tests. The present study investigated whether the L. camara extract (ACE) also exerts these effects. The ACE toxicity was studied in male mice, and the percentage of mortality recorded 7 days after treatment was assessed. The ACE was evaluated as an antinociceptive agent in the hot plate, tail-flick and acetic acid writhing tests at a nontoxic dose of 1.0 g/Kg. The results showed that 1.5 g/Kg of ACE was not able to cause death, and doses of 3.0 and 4.0 g/Kg caused 50% and 60% death, respectively, in male mice. In all of the antinociceptive tests, 1 g/Kg of ACE markedly reduced responses to pain. Our findings suggest that ACE may have active anti-inflammatory and antinociceptive properties in much smaller doses than toxic.

scholarly journals Flavonoids from the Bark of Artocarpus integer var. silvestris and their Anti-inflammatory Properties

2016 ◽  
Vol 11 (9) ◽  
pp. 1934578X1601100
Author(s):  
Masuri Kama Kamaruddin Shah ◽  
Hasnah Mohd Sirat ◽  
Shajarahtunnur Jamil ◽  
Juriyati Jalil
Keyword(s):  
2D Nmr ◽  
Prostaglandin E ◽  
Spectroscopic Techniques ◽  
Dependent Inhibition ◽  
Pure Compounds ◽  
Dose Dependent Inhibition ◽  
Cox 2 ◽  
Anti Inflammatory ◽  
Dose Dependent ◽  
Radioimmunoassay Method

A new pyranoflavone, methoxycyclocommunol (1) together with four known flavonoids, artonin F (2), heteroflavanone A (3), cudraflavone C (4) and cyclocommunol (5) were isolated from the bark of Artocarpus integer var. silvestris Corner. Their structures were elucidated through extensive spectroscopic techniques (UV, IR, MS, 1D-NMR and 2D-NMR) and by comparison with literature data. All the pure compounds were tested for their anti-inflammatory activities by using screening kit and radioimmunoassay methods. In a 15-lipoxygenase (15-LOX) inhibitory assay, compounds 1, 2, 4 and 5 gave weak percentages of inhibition, 16.5, 18.3, 17.6, 10.2%, respectively at the concentration of 100 μM. Compounds 1, 3 and 4, however, showed strong dose-dependent inhibition towards prostaglandin E2 (PGE2) production in lipopolysaccharide-induced human whole blood using a radioimmunoassay method with IC50 values of 4.3, 0.8, and 0.07 μM, respectively suggesting that they strongly exhibited cyclooxygenase-2 (COX-2) activity.

Sign in / Sign up

Export Citation Format

Share Document