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锯齿草(Pluchea sagittalis(Lam.)Cabrera)乙醇提取物的镇痛和胃保护作用。

Antinociceptive and gastroprotective actions of ethanolic extract from Pluchea sagittalis (Lam.) Cabrera.

机构信息

Laboratory of Neurobiology of Pain and Inflammation, Department of Physiological Sciences, Center of Biological Sciences, Universidade Federal de Santa Catarina, Florianópolis, SC 88040-900, Brazil.

出版信息

J Ethnopharmacol. 2011 Jun 1;135(3):603-9. doi: 10.1016/j.jep.2011.03.006. Epub 2011 Mar 15.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Pluchea sagittalis, an herbaceous plant widely distributed in South America, is used in folk medicine for the treatment of digestive diseases and inflammation.

AIM OF THE STUDY

This study was designed to investigate the antinociceptive and gastroprotective effects of the ethanolic extract (EE) of aerial parts from Pluchea sagittalis in rodents.

MATERIALS AND METHODS

The antinociceptive effects of EE was evaluated in mice after oral administration in chemical tests (acetic-acid, glutamate and formalin) or by biting behavior following intrathecal administration of cytokines such as interleukin-1beta (IL-1β) and tumor necrosis factor-alpha (TNF-α) in mice. Furthermore, rats were treated with EE and subsequently exposed to acute gastric lesions induced by 80% ethanol. Afterwards the gastric lesion extension and the mucus levels of gastric mucosa were measured.

RESULTS

The oral administration of EE showed a dose-dependent inhibition of acetic acid-induced abdominal constrictions and glutamate-induced pain in mice, with ID(50) values of 624.0 (523.0-746.0) mg/kg and 368.0 (216.0-628.0) mg/kg, respectively. In the formalin test, the EE also produced significant inhibition of the inflammatory phase, with an ID(50) value of 411.0 (183.0-721.0) mg/kg; however, it was ineffective in the neurogenic phase caused by formalin. In addition, oral treatment with EE caused a significant inhibition of biting behavior induced by i.t. injection of interleukin-1β (IL-1β) and tumor necrosis factor-α (TNF-α). The antinociception caused by the EE (300 mg/kg, p.o.) was not reversed by naloxone (1 mg/kg, i.p.) when assessed in the acetic acid writhing test. The EE (300-1000 mg/kg, p.o.) did not affect the motor coordination of animals in an open-field model. Oral treatment with the EE protected rats against gastric lesions induced by ethanol, with an ID(50) value of 55.0 (46.6-64.9) mg/kg, and increased the mucus levels of gastric mucosa to levels found in the non-lesioned group.

CONCLUSIONS

The mechanism by which the extract produced antinociception still remains unclear, but this effect seems to be primarily related to the modulation or inhibition of the action of pro-inflammatory mediators. Furthermore, these data support, at least in part, the ethnomedical use of Pluchea sagittalis.

摘要

民族药理学相关性

Pluchea sagittalis 是一种广泛分布于南美洲的草本植物,在民间医学中用于治疗消化疾病和炎症。

研究目的

本研究旨在研究 Pluchea sagittalis 地上部分的乙醇提取物(EE)在啮齿动物中的镇痛和胃保护作用。

材料和方法

通过口服给予 EE 后,在化学试验(乙酸、谷氨酸和甲醛)中或通过鞘内给予白细胞介素-1β(IL-1β)和肿瘤坏死因子-α(TNF-α)等细胞因子后通过咬行为评估 EE 的镇痛作用。此外,用 EE 处理大鼠,然后使其暴露于 80%乙醇引起的急性胃损伤。然后测量胃损伤的延伸和胃粘膜的粘液水平。

结果

EE 的口服给药显示出剂量依赖性抑制乙酸引起的腹部收缩和谷氨酸引起的疼痛,ID(50)值分别为 624.0(523.0-746.0)mg/kg 和 368.0(216.0-628.0)mg/kg。在甲醛试验中,EE 还显著抑制了炎症期,ID(50)值为 411.0(183.0-721.0)mg/kg;然而,它对甲醛引起的神经原性期无效。此外,口服 EE 治疗可显著抑制鞘内注射白细胞介素-1β(IL-1β)和肿瘤坏死因子-α(TNF-α)引起的咬行为。在乙酸扭体试验中,EE(300mg/kg,po)引起的镇痛作用不受纳洛酮(1mg/kg,ip)逆转。EE(300-1000mg/kg,po)对动物在开阔场模型中的运动协调没有影响。口服 EE 治疗可预防乙醇引起的胃损伤,ID(50)值为 55.0(46.6-64.9)mg/kg,并增加胃粘膜的粘液水平至未损伤组的水平。

结论

提取物产生镇痛作用的机制尚不清楚,但这种作用似乎主要与促炎介质的调节或抑制有关。此外,这些数据至少部分支持 Pluchea sagittalis 的民族医学用途。

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