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1.
J Evid Based Complementary Altern Med ; 21(4): 271-6, 2016 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-26427790

RESUMO

Asafetida is well known for its medicinal and therapeutic values in Iranian folk medicine. This study was conducted to investigate the antinociceptive and anti-inflammatory effects of asafetida. In hot plate test, asafetida exhibited a significant antinociceptive effect at all administered doses and the most effective dose was 10 mg/kg. The highest maximum potent effect was observed 15 minutes after asafetida administration. The antinociceptive effect of asafetida was not reversed by administration of any antagonist used in this study but asafetida showed a remarkable antioxidant and also inhibitory action against lipoxygenase activity. Paw weight was significantly reduced only in treated animals with 2.5 mg/kg asafetida. Results clearly indicate that the asafetida could be a potential source of anti-inflammatory and analgesic agent. These effects may be due to its effective constituents such as monoterpenes, flavonoids and phenolic components that have antioxidant properties and inhibit lipoxygenase activity.


Assuntos
Analgésicos , Anti-Inflamatórios , Ferula/química , Gomas Vegetais , Resinas Vegetais , Ácido Acético , Analgésicos/análise , Analgésicos/farmacologia , Animais , Anti-Inflamatórios/análise , Anti-Inflamatórios/farmacologia , Antioxidantes/química , Antioxidantes/farmacologia , Comportamento Animal/efeitos dos fármacos , Edema , Peroxidação de Lipídeos/efeitos dos fármacos , Masculino , Camundongos , Manejo da Dor , Medição da Dor , Gomas Vegetais/química , Gomas Vegetais/farmacologia , Resinas Vegetais/química , Resinas Vegetais/farmacologia
2.
J Ayurveda Integr Med ; 6(3): 175-80, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-26604552

RESUMO

BACKGROUND: In Ayurveda and traditional medicines of different countries such as Iran, America and Brazil, asafoetida has been used as an aphrodisiac agent. OBJECTIVE: The present study was aimed to evaluate the effectiveness of asafoetida on spermatic and testicular parameters in treated rats. MATERIALS AND METHODS: A total of 30 male Wistar rats divided equally to five groups (one control and four test groups receiving 25, 50,100 and 200 mg/kg asafoetida respectively). After 6 weeks, a small part of the cauda epididymis of each rat was dissected, and the spermatic parameters were evaluated for at least 200 spermatozoa of each animal. Testis of all rats was harvested for pathologic examination. The testosterone concentration of serum was also determined. Data were statistically assessed by one-way ANOVA and value of P < 0.05 was considered as the level of significance. RESULTS: This study indicated that the asafoetida significantly increased the number and viability of sperms (P < 0.05). Histological study showed that spermatogenesis process and numbers of Leydig cells were increased with increasing the dose, but the Leydig cells become vacuolated. Johnsen score in experimental groups was increased compared to control although this difference was not significant (P > 0.05). CONCLUSION: Asafoetida showed a positive effect on spermatic parameters although the histopathological effects on the testis were observed, particularly at high doses.

3.
J Ayurveda Integr Med ; 6(1): 19-23, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-25878459

RESUMO

BACKGROUND: In Iranian traditional medicine, gum obtained from Astragalus gummifer and some other species of Astragalus was used as analgesic agent. OBJECTIVE: In this study, we investigated the antinociceptive effect of several concentrations (125, 250, and 500 µg/kg body weight) of Astragalus gummifer gum (AGG) on thermal and acetic acid induced pain in mice. MATERIALS AND METHODS: AGG was dissolved in distillated water and injected i.p to male mice 15 minute before the onset of experiment. Writhing and hot-plate tests were applied to study the analgesic effect of AGG and compared with that of diclofenac sodium (30 mg/kg, i.p.) or morphine (8 mg/kg, i.p). To investigate the mechanisms involved in antinociception, yohimbine, naloxone, glibenclamide, and theophylline were used in writhing test. These drugs were injected intraperitoneally 15 min before the administration of AGG. The number of writhes were counted in 30 minutes and analyzed. RESULTS: AGG exhibited a significant antinociceptive effect and the most effective dose of AGG was 500 µg/kg. The most maximum possible effect (%MPE) was observed (117.4%) 15 min after drug administration. The %inhibition of acetic acid-induced writhing in AGG 125, 250 and 500 was 47%, 50% and 54% vs %15 of control and 66.3% of diclofenac sodium group. The antinociceptive effect induced by this gum in the writhing test was reversed by the systemic administration of yohimbine (α2-adrenergic antagonist), but naloxone, glibenclamide, and theophylline did not reverse this effect. CONCLUSIONS: The findings of this study indicated that AGG induced its antinociceptive through the adrenergic system.

4.
Am J Alzheimers Dis Other Demen ; 30(6): 607-12, 2015 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-25788433

RESUMO

In Iranian traditional medicine, asafoetida is introduced as a valuable remedy for nervous disorders. Dementia was induced by injection of d-galactose and NaNO2 for 60 consecutive days. Animals were divided into normal control (NC), dementia control (DC), dementia prophylactic (DP), and dementia treated (DT). The learning and memory functions were examined by 1-way active and passive avoidance tests, using a shuttle box device. Avoidance response in training tests and 1 and 3 weeks later was significantly increased in NC, DP, and DT groups compared to the DC group. Step through latency in all groups was significantly greater than the DC group. Total time spent in light room, which shows the memory retention ability, in DP, NC, and DT was significantly greater than the DC group. Our findings indicate that asafoetida could prevent and treat amnesia. These beneficial effects maybe related to some constituent's effectiveness such as ferulic acid and umbelliferone.


Assuntos
Comportamento Animal/efeitos dos fármacos , Demência/tratamento farmacológico , Ferula , Transtornos da Memória/tratamento farmacológico , Fitoterapia/métodos , Preparações de Plantas/farmacologia , Animais , Demência/induzido quimicamente , Demência/prevenção & controle , Modelos Animais de Doenças , Conservantes de Alimentos/administração & dosagem , Conservantes de Alimentos/farmacologia , Galactose/administração & dosagem , Galactose/farmacologia , Irã (Geográfico) , Transtornos da Memória/induzido quimicamente , Transtornos da Memória/prevenção & controle , Camundongos , Preparações de Plantas/administração & dosagem , Nitrito de Sódio/administração & dosagem , Nitrito de Sódio/farmacologia
5.
Avicenna J Phytomed ; 4(1): 53-8, 2014 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-25050301

RESUMO

OBJECTIVE: Many biological studies have been done to determine the activity of medicinal plants on gastrointestinal function. Since acetylcholine is the major transmitter involved in the gastrointestinal motility and there are some evidences regarding the cholinergic modulatory effect of hops extract, in the present study spasmolytic and antispasmodic action of hops (Humulus lupulus) on acetylcholine-induced contraction in isolated rat's ileum was evaluated. MATERIAL AND METHODS: In this study, pieces of isolated rat's ileum were mounted in the internal chamber of an organ bath which was filled with Tyrode's solution and tightly tied to the lever of an isotonic transducer. The contractile responses were recorded by using an oscillograph device. In the presence of normal saline and different concentrations of hops (0.1, 0.3, and 0.5 mg/ml), the amplitude of contractions induced by10(-12) up to 10(-2) M acetylcholine was determined. The spasmolytic action of the same extract concentrations was also examined on contraction induced by 10(-4) acetylcholine. RESULTS: Our findings indicate that hops extract reduces acetylcholine-induced contraction in all concentrations. The significant inhibitory effects of 0.1, 0.3, and 0.5 mg/ml hops extract on contraction induced by 10(-3) M acetylcholine were 81.9, 77, and 29.3, respectively (p<0.05). CONCLUSION: According to our findings, hops extract poses a potent spasmolytic and antispasmodic action on acetylcholine-induced contraction in isolated rat's ileum which may be mediated by cholinergic systems.

6.
J Acupunct Meridian Stud ; 2(1): 75-8, 2009 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-20633478

RESUMO

AIMS: There are many biological investigations for determining an effective cure for the dysfunction of gastrointestinal tracts, using herbal medicine. It has been reported that Carum Copticum is a bactericidal agent and possesses anticholinergic, antihistaminic and b-adrenergic stimulatory effects in some tissues. However, these effects of Carum Copticum on mechanical activities of isolated intestine are not clearly identified yet. The present study has been designed to find out the specific effects of Carum Copticum on mechanical activity of isolated rat's ileum. MATERIALS AND METHODS: In this study rat's ileum contraction was recorded through an isolated tissue chamber in an organ bath by using isotonic transducer and oscillographic device. The effect of Carum Copticum extract on acetylcholine induced contraction in isolated rat's ileum was evaluated. RESULTS: Our findings showed that 1% aqueous extract of Carum Copticum reduces the basal contractile activity of rat's ileum. The extract also reduced acetylcholine induced contraction to 40% of its maximum response. The inhibitory action of Carum Copticum extract on acetylcholine induced contraction was similar but slower than that of atropine sulfate. CONCLUSION: The results of this study showed an inhibitory effect of Carum Copticum extract on acetylcholine induced contraction in rat's ileum.


Assuntos
Acetilcolina/farmacologia , Carum/química , Íleo/fisiologia , Contração Muscular/efeitos dos fármacos , Extratos Vegetais/farmacologia , Animais , Íleo/efeitos dos fármacos , Técnicas In Vitro , Masculino , Ratos
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