Analgesic,antipyretic and antiinflammatory effects of Achillea ageratum

The aqueous and methanol extracts of Achillea ageratum L. (Asteraceae) have been evaluated for analgesic, antipyretic and antiinflammatory properties in mice and rats in several experimental models. The aqueous extract exhibited significant activity in the analgesic and antiinflammatory assays but was unable to reduce hyperthermia. Moreover, the methanol extract exerted effects in three pharmacological actions. The phytochemical investigation of this latter extract revealed the presence of flavonic compounds: luteolin, quercetin and 7-O-β-luteolin. © 1997 John Wiley & Sons, Ltd.     

Antiinflammatory activity of the iridoids kutkin,picroside-1 and kutkoside from Picrorhiza kurrooa

Powdered roots of Picrorhiza kurrooa (PK), its alcoholic extract (AEPK) and active constituents kutkin, picroside-1 and kutkoside demonstrated antiinflammatory activity (AIA) in a variety of test models. Significant AIA was recorded in adjuvant-induced and formaldehyde arthritis in rats and mice. In carrageenan-induced oedema inhibitory activity was remarkably enhanced upon intraperitoneal treatment in rats and mice. Kutkin exhibited significant action in dextran-induced oedema in rats. It inhibited acetic acid induced vascular permeability in mice and leucocyte migration in rats. Kutkin lacked any analgesic, antipyretic or ulcerogenic effect.     

Antipyretic,hypothermic and antiinflammatory activities and metabolites from Solanum ligustrinum Lood.

The acute toxicities of the global methanol extract of Solanum ligustrinum (Solanaceae) and the crude steroidal glycoalkaloids mixture were determined. The antipyretic, hypothermic and antiinflammatory activities of aqueous, global methanol, petroleum ether, dichloromethane and methanol extracts and crude steroidal glycoalkaloids mixture of the aerial parts were evaluated. All the extracts and the crude steroidal glycoalkaloids mixture were inactive in the hypothermic activity assay, nevertheless, they showed antipyretic and antiinflammatory activities. Scopoletin and β-sitosterol 3-O-β-D-glucoside were isolated and identified from the dichloromethane extract. The impure coumarin fraction showed antipyretic and antiinflammatory activities and β-sitosterol glucoside exhibited antiinflammatory activity. In the light of the results of several NOE experiments, the H-5 and H-8 signals in the ¹H-NMR spectra of scopoletin were reassigned. The methanol global extract yielded a crude steroidal glycoalkaloids mixture with antipyretic and antiinflammatory effects. © 1998 John Wiley & Sons, Ltd.     

Some effects of Salvia aegyptiaca L. on the central nervous system in mice

Salvia aegyptiaca L. is used for treating various unrelated conditions that include nervous disorders, dizziness, trembling, diarrhoea and piles. This work examines some effects of the crude acetone and methanol extracts of the plant given at single oral doses of 0.25, 0.5, 1 or 2 g/kg, on the central nervous system (CNS) in mice. The extracts were also tested for anti-inflammatory and antipyretic actions. Several models of nociception have been used to examine the analgesic effect of the extract. In treated mice, the extracts caused dose-related inhibition of acetic acid-induced abdominal constriction, and significantly reduced formalin-induced pain. Treatment with the extracts at doses of 0.5 and 1 g/kg significantly increased the reaction time in the hot-plate test. In treated mice both extracts caused significant and dose-related impairment of the sensorimotor control and motor activity. Treatment with both extracts did not significantly affect the rectal temperature of normothermic mice. The methanol extract (0.5 and 1.0 g/kg) did not affect the rectal temperature of hyperthermic mice, but the acetone extract was effective in significantly reducing the rectal temperature of hyperthermic mice, 0.5 and 1 h after administration of the extract at doses of 0.25-2 g/kg. It is concluded that the crude methanol and acetone extracts of S. aegyptiaca have CNS depressant properties, manifested as antinociception and sedation. Both extracts have some anti-inflammatory and antipyretic actions. On the whole, the acetone extract appeared to be slightly more effective than the methanol extract in this regard.     

Pharmacological activities of extracts of Daniellia oliveri (Rolfe) Hutch. and Dalz. (Leguminosae)

Extracts of the stem bark of Daniellia oliveri using hexane, ethyl acetate and methanol were tested for analgesic, antipyretic and antiinflammatory activities. The hexane extract exhibited a dose related analgesic activity whilst the methanolic extract was active in the induced inflammatory condition. The ethyl acetate extract was relatively inactive and none of the extracts showed any antipyretic activity. Metabolic cage studies showed that a 70% ethanolic extract of the bark caused significant decreases in body weight, food intake, urine and stool output of rats. This extract also exhibited a competitive antagonism on histamine-induced contractions of the guinea-pig ileum and a non-competitive inhibition of acetyl choline-induced contraction of the frog rectus abdominis muscle.     

Analgesic and antiinflammatory properties of Scoparia dulcis L. Extracts and glutinol in rodents

The analgesic, antiinflammatory and antipyretic activities of the water (WE) and ethanolic (EE) extracts of Scoparia dulcis L. were tested in mice and rats. Both extracts (0.5 and 1 g/kg) p.o., prolonged the sleeping time induced by pentobarbital in mice, EE being more active than WE. Injections of EE (0.5–2 mg/kg i.v.) to anaesthetized rats induced a dose-related hypertension inhibited by alpha-blocker drugs; the hypertension was not obtained after oral treatment. EE (0.25-1 g/kg p.o.) but not WE, reduced writhings induced by acetic acid in mice. Glutinol (30 mg/kg p.o.), a major triterpene obtained from EE, produced the same effect. The tail flick response of mice was not influenced by either extract. EE (0.5 and 1 g/kg) and glutinol (30 mg/kg) p.o., reduced the paw oedema and pleurisy induced by carrageenin in rats, but only EE (1 g/kg) reduced the paw oedema induced by dextran or histamine. No effect of EE was detected on chronic inflammation induced by cotton pellets and in yeast-induced hyperthermia in rats. The results indicate that the extract of S. dulcis is endowed with analgesic effects probably related to the antiinflammatory activity of the plant. Those effects are related mainly to the presence of glutinol and flavonoids, which exert their action on the early phase of the acute inflammatory process.     

Anti-inflammatory activity of Lannea coromandelica bark extract in rats

Oral administration of an ethanolic extract of Lannea coromandelica (ELC) demonstrated a dose related antiinflammatory activity (AIA) in carrageenan and dextran induced oedema and adjuvant induced arthritis in rats. ELC reduced the pleural exudate volume and inhibited leucocyte migration in carrageenan-induced pleurisy in rats. It lacked analgesic, antipyretic or ulcerogenic effect and failed to exhibit any effect in cotton pellet granuloma. It did not prolong the gestation period, parturition time in pregnant rats or the onset time of diarrhoea in rats induced by castor oil. The ALD₅₀ is greater than 2 g/kg p.o. in mice.     

A preliminary study of Cedronella canariensis (L.) var. Canariensis extracts for antiinflammatory and analgesic activity in rats and mice

Several extracts and fractions from Cedronella canariensis (L.) have been submitted to analgesic, antipyretic and antiinflammatory tests on rats and mice. The experimental results obtained justified the utilization of this species as an anticatarrh and antiinfluenza agent in Canarian folk medicine. Its acute toxicity turned out to be low as measured in mice.     

Preliminary pharmacologic evaluation of crude whole plant extracts of Elephantopus scaber. Part I: In vivo studies.

Elephantopus scaber has been used in Brazil as a traditional remedy to cause diuresis, antipyresis and to eliminate bladder stones. In the current study, aqueous and hydroalcoholic extracts of whole plants were tested for acute toxicity, analgesic, antipyretic, antiinflammatory, cardiovascular, diuretic and constipating activities. Both extracts (0.3-6 g/kg i.p.) induced writhing, loss of muscle tone, ataxia, prostration and death in mice. No analgesic effects of these extracts were detected using mouse hot-plate and acetic acid-induced writhing tests. Both extracts failed to modify diuresis or carrageenan-induced rat paw edema. In contrast, given intraperitoneally, both reduced brewer's yeast-induced hyperthermia in rats, but when given orally did not affect it. Moreover, the aqueous extract decreased the intestinal transit time in mice while the hydroalcoholic extract increased it. Finally, these extracts, given intravenously, reduced blood pressure and heart rate in rats; these effects could be blocked by atropine but not by co-administration of pyrilamine and cimetidine.     

Anti-inflammatory and antipyretic properties of Clerodendrum petasites S. Moore

The methanol extract from Clerodendrum petasites S. Moore (CP extract) was assessed for anti-inflammatory and antipyretic activities on the experimental animal models. It was found that CP extract possessed moderate inhibitory activity on acute phase of inflammation in a dose-related manner as seen in ethyl phenylpropiolate-induced ear edema (ED(50)=2.34 mg/ear) as well as carrageenin-induced hind paw edema (ED(30)=420.41 mg/kg) in rats. However, CP extract did not elicit any inhibitory effect on arachidonic acid-induced hind paw edema in rats. In subchronic inflammatory model, CP extract provoked a significant reduction of transudation but had no effect on proliferative phase when tested in cotton pellet-induced granuloma model. CP extract also reduced the alkaline phosphatase activity in serum of rats in this animal model. Moreover, CP extract possessed an excellent antipyretic effect when tested in yeast-induced hyperthermic rats. It is postulated that the anti-inflammatory and antipyretic effects of CP extract are caused by the inhibition of the prostaglandin synthesis. Anyhow, CP extract did not possess any analgesic activity in acetic acid-induced writhing response in mice. The results obtained show that C. petasites has beneficial properties since it possesses potent antipyretic and moderate anti-inflammatory activities without ulcerogenic effect.     

Studies on the Antiulcer Activity of the Chloroform Fraction of Calotropis procera Root Extract

Calotropis procera has been widely used in the Indian traditional medicinal system for the treatment of a variety of disease conditions. Earlier studies in our laboratory revealed that the chloroform fraction of C. procera root extract possesses significant analgesic, antipyretic and antiinflammatory activity. Further studies also revealed that, unlike the NSAIDs, C. procera simultaneously possesses significant antiulcer activity. It is well established that the NSAIDs are potentially ulcerogenic and they exert their antiinflammatory activity following inhibition of prostaglandin synthesis (owing to the blockade of the cyclooxygenase pathway), thereby leading to overproduction of leukotrienes and other related products of arachidonic acid metabolism which in turn have potential ulcerogenic activity. We accordingly attempted to evaluate the antiulcer activity of C. procera using different in vivo ulcer models. The results of the present study revealed that C. procera significantly inhibited aspirin, reserpine, absolute alcohol and serotonin-induced gastric ulcerations in rats. The same also protected the gastric mucosa from aspirin-induced ulceration in pyloric-ligated rats and significant protection was observed in histamine-induced duodenal ulcers in guinea-pigs. © 1997 by John Wiley & Sons, Ltd.     

Analgesic and antipyretic effects of Myrica salicifolia (Myricaceae)

Myrica salicifolia Hoechst (Myricaceae) root extract was found to have analgesic activity in mice. In rats there was antipyretic but no antiinflammatory activity.     

Pharmacological evaluation of Hoslundia opposita extract in rodents

A chloroform extract of the dried root of Hoslundia opposita was studied for its analgesic, antipyretic and antiinflammatory activities. A significant protection against the acetic acid-induced writhing response in mice, and a marked lowering of the body temperature of hyperthermic mice was observed. A significant inhibition of the carrageenan-induced rat hind paw oedema was also produced. Our preliminary screening thus confirms the folklore use of Hoslundia opposita in various ailments. © 1998 John Wiley & Sons, Ltd.     

Analgesic and antiinflammatory effects of mollic acid glucoside, a 1 alpha-hydroxycycloartenoid saponin extractive from Combretum molle R. Br. ex G. Don (Combretaceae) leaf

The analgesic and antiinflammatory properties of mollic acid glucoside (MAG), a 1 alpha-hydroxycycloartenoid extract from Combretum molle leaf, have been investigated in mice and rats. The effects of graded doses of mollic acid glucoside (MAG, 5-80 mg/kg i.p.) were examined against thermally- and chemically-induced nociceptive pain in mice. Furthermore, the effects of graded doses of the plant extract (MAG, 5-80 mg/kg p.o.) were also investigated on rat paw oedema induced by subplantar injections of fresh egg albumin (0.5 mg/kg). Morphine (MPN, 10 mg/kg i.p.) and diclofenac (DIC, 100 mg/kg i.p.) were used as reference analgesic and antiinflammatory agents for comparison, respectively. Like DIC (100 mg/kg i.p.) and MPN (10 mg/kg i.p.), MAG (5-80 mg/kg i.p.) produced dose-dependent, significant (p < 0.05-0.001) analgesic effects against thermally and chemically induced nociceptive pain in mice. The extractive (MAG, 5-80 mg/kg i.p.) also significantly reduced (p < 0.05-0.001) rat paw oedema induced by subplantar injections of fresh egg albumin in a dose-related fashion. However, the extract (MAG, 5-80 mg/kg i.p.) was found to be less potent than diclofenac (DIC) as an analgesic or antiinflammatory agent. Experimental evidence obtained from this laboratory animal study indicates that the Combretum molle leaf extractive (MAG) possesses analgesic and antiinflammatory properties, and thus lend pharmacological credence to the folkloric, ethnomedical uses of the plant's leaf in the management, control and/or treatment of painful, arthritic and other inflammatory conditions in some rural communities of southern Africa.     

Studies on the anti-inflammatory, antipyretic and analgesic properties of Alstonia boonei stem bark

The methanol extract of the stem bark of Alstonia boonei was investigated for anti-inflammatory property. The analgesic and antipyretic properties of the extract was also evaluated. The extract caused a significant (P<0.05) inhibition of the carrageenan-induced paw oedema, cotton pellet granuloma, and exhibited an anti-arthritic activity in rats. Vascular permeability induced by acetic acid in the peritoneum of mice was also inhibited. The extract also produced marked analgesic activity by reduction of writhings induced by acetic acid, as well as the early and late phases of paw licking in mice. A significant (P<0.05) reduction in hyperpyrexia in mice was also produced by the extract. This study has established anti-inflammatory, analgesic and antipyretic activities of the stem bark of A. boonei.     

Analgesic and antipyretic properties of Euphorbia royleana latex

The ethyl acetate fraction (EA) from the residue of an 85% ethanol extract of the latex of Euphorbia royleana (Euphorbiaceae) was investigated for antipyretic and analgesic properties. The results showed a dose related peripheral analgesic effect. The fraction assayed exhibited a significant antipyretic effect in hyperthermic rats and rabbits. The oral LD₅₀ was more than 2 g/kg in rats and mice. © 1997 John Wiley & Sons, Ltd.     

小叶黑柴胡的药理作用研究

小叶黑柴胡水煎剂与粗皂甙对菌苗致热家兔有明显解热作用。粗皂甙对小鼠扭体有明显镇痛作用。乙醚提取物与粗皂甙对二甲苯所致小鼠耳壳肿胀和角叉菜胶致小鼠足跖肿胀均有明显抑制作用,这些作用与相同剂量的北柴胡之间无显著差异,它们之间的急性毒性亦无显著差异。     

两种不同挥发油含量柴胡制剂药效作用研究

目的:对比两种不同挥发油含量柴胡制剂的抗炎、镇痛、解热作用。方法:分别采用二甲苯致炎剂所致小鼠耳廓肿胀实验,醋酸引起小鼠疼痛扭体实验,干酵母致大鼠发热实验,观察两种柴胡制剂的抗炎、镇痛、解热作用,并比较二者差异。结果:采用抗炎、镇痛、解热三种动物模型研究表明,普通柴胡浸膏5g生药/kg、10g生药/kg,富集挥发油的柴胡浸膏5g生药/kg、10g生药/kg均可显著减轻二甲苯所致的小鼠耳肿胀,减少醋酸所致的小鼠扭体反应次数,降低干酵母引起的大鼠体温升高,其中富集挥发油的柴胡浸膏的抗炎活性优于普通柴胡浸膏,但镇痛和解热活性两种浸膏无显著性差异。结论:两种不同挥发油含量柴胡浸膏均具有明显的抗炎、镇痛和解热作用,但柴胡挥发油抗炎活性较高。     

Studies on the anti-inflammatory, antipyretic and analgesic properties of the leaves of Aegle marmelos Corr

The serial extracts of the leaves of Aegle marmelos Corr. were investigated for anti-inflammatory property. The analgesic and antipyretic properties were also evaluated. The most of the extracts derived from the plant Aegle marmelos caused a significant inhibition of the carrageenan-induced paw oedema and cotton-pellet granuloma in rats. The extracts also produced marked analgesic activity by reduction the early and late phases of paw licking in mice. A significant reduction in hyperpyrexia in rats was also produced by the most of the extracts. This study was established anti-inflammatory, antinociceptive and antipyretic activities of the leaves of Aegle marmelos.     

栽培苦参与野生苦参的药效学研究

目的:比较栽培与野生苦参的清热、利尿、镇痛方面的药效学作用。方法:以干酵母致大鼠高热模型比较栽培苦参与野生苦参的解热作用;以代谢笼收集大鼠不同时间点的排尿量和总尿量比较栽培与野生苦参的利尿效果;采用热板和扭体法比较观察其对小鼠的镇痛作用。结果:栽培与野生苦参(1,2,4 g.kg-1剂量)均能明显降低酵母菌致热模型大鼠的体温;明显增加大鼠不同时间段的排尿量和排尿总量;栽培与野生苦参3,6 g.kg-1剂量均可明显提高小鼠的热板痛阈值、明显延长小鼠出现扭体的潜伏期并明显减少小鼠的扭体次数,表明其具有非常明显的镇痛作用。结论:栽培苦参与野生苦参都具有明显的清热、利尿和镇痛方面的作用,药效学作用强度比较野生与栽培苦参无显著差异,本实验结果为栽培苦参代替野生苦参提供了实验依据。