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内源性大麻素系统参与脂多糖诱导的唾液分泌抑制。

Participation of the endocannabinoid system in lipopolysaccharide-induced inhibition of salivary secretion.

机构信息

Cátedra de Fisiología, Universidad de Buenos Aires, Argentina.

出版信息

Arch Oral Biol. 2010 Aug;55(8):583-90. doi: 10.1016/j.archoralbio.2010.05.006. Epub 2010 Jun 9.

Abstract

OBJECTIVE

The aim of the present paper was to assess whether lipopolysaccharide (LPS)-induced inhibition of salivary secretion involves the activation of the endocannabinoid system and the participation of tumor necrosis factor (TNF)alpha in the submandibular gland.

DESIGN

Pharmacological approaches were performed by using CB1 and/or CB2 cannabinoid receptor antagonists, AM251 and AM630, respectively, injected into the submandibular gland, to study the participation of the endocannabinoid system in LPS inhibitory effects on metacholine-induced salivary secretion. To assess the participation of TNFalpha on LPS inhibitory effects, salivary secretion was studied in LPS treated rats after the intraglandular injection of etanercept, a soluble form of TNF receptor which blocks TNFalpha action. Finally, to evaluate the possible interplay between endocannabinoids and TNFalpha on the submandibular gland function reduced during LPS challenge, the salivary secretion was studied after the intraglandular injection of this cytokine alone or concomitantly with AM251 and AM630.

RESULTS

AM251 and AM630, injected separately or concomitantly, partially prevented LPS-induced inhibition of salivation. Also, anandamide synthase activity was increased in submandibular glands extracted from rats 3h after LPS injection, suggesting that the endocannabinoid system was activated in response to this challenge. On the other hand, etanercept, prevented the inhibitory effect of LPS on salivary secretion and moreover, TNFalpha injected intraglandularly inhibited salivary secretion, being this effect prevented by AM251 and AM630 injected concomitantly.

CONCLUSION

The present results demonstrate the participation of the endocannabinoid system and TNFalpha on salivary responses during systemic inflammation induced by LPS.

摘要

目的

本研究旨在评估脂多糖(LPS)诱导的唾液分泌抑制是否涉及内源性大麻素系统的激活以及肿瘤坏死因子(TNF)α在颌下腺中的参与。

设计

通过向颌下腺内注射 CB1 和/或 CB2 大麻素受体拮抗剂 AM251 和 AM630,分别研究内源性大麻素系统在 LPS 对乙酰甲胆碱诱导的唾液分泌抑制作用中的参与。为了评估 TNFα 在 LPS 抑制作用中的参与,在 LPS 处理的大鼠中研究了 TNF 受体可溶性形式etanercept (可阻断 TNFα 作用)的颌下腺内注射后对 LPS 抑制作用的影响。最后,为了评估内源性大麻素和 TNFα 在 LPS 刺激期间对颌下腺功能降低的相互作用,在单独或同时注射内源性大麻素和 TNFα 后研究了唾液分泌。

结果

AM251 和 AM630 分别或同时注射可部分预防 LPS 诱导的唾液分泌抑制。此外,在 LPS 注射后 3 小时提取的颌下腺中,发现了更多的花生四烯酸酰胺合成酶活性,表明内源性大麻素系统对这种刺激做出了反应。另一方面,etanercept 可预防 LPS 对唾液分泌的抑制作用,而且,TNFα 颌下腺内注射可抑制唾液分泌,这种作用可被同时注射的 AM251 和 AM630 预防。

结论

本研究结果表明,内源性大麻素系统和 TNFα 参与了 LPS 诱导的全身炎症期间的唾液反应。

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