Anandamide

本公司产品仅用于科研实验，不得用于人体或动物的临床与诊断

Anandamide 是一种免疫调节剂，不仅通过大麻素受体（CB1 和 CB2）发挥作用，还通过中枢神经系统中的其他靶标（例如 GPR18/GPR55）发挥作用。

Anandamide, an immune modulator, acts via not only cannabinoid receptors (CB1 and CB2) but also other targets (e.g., GPR18/GPR55) in the central nervous system.(In Vitro):Anandamide, acting via CB2 receptors, alleviates lipopolysaccharide (LPS)-induced neuroinflammation in rat primary microglial cultures. Endocannabinoids, especially Anandamide (AEA), can activate numerous other receptors like PPARS, TRPV1, and GPR18/GPR55 .(In Vivo):Anandamide is an endocannabinoid binding both CB1R and CB2R. To evaluate the impact of CBR activation on whole-body glucose homeostasis, glucose tolerance is assessed after a single intraperitoneal Anandamide injection (10 mg/kg). The increase in glycemia in response to glucose ingestion is considerably smaller in mice treated with Anandamide compared with control. It is associated with an improvement of glucose tolerance as illustrated by the AUC0-2h calculations.

Anandamide (0-250 μg/ml, 1 h) inhibits C. albicans hyphal growth and prevents hyphal adherence to epithelial cells.Anandamide (0-250 μg/ml, 2 h) alters the expression of genes involved in adhesion and hyphal morphogenesis.Anandamide reduces tau phosphorylation through the inhibition of the activity of protein kinases. RT-PCRCell Line:HeLa cervical epithelial cells Concentration:0, 10, 50, 125, 250 μg/ml Incubation Time:2 h Result:Repressed the expression of the HWP1 and ALS3 adhesins involved in Candida adhesion to epithelial cells and the HGC1, RAS1, EFG1 and ZAP1 regulators of hyphal morphogenesis and cell adherence. Increased the expression of NRG1, a transcriptional repressor of filamentous growth.

Anandamide (10 mg/kg, IP, once) considerably lowers the increase of glycemia in response to glucose ingestion compared with control, and this is associated with an improvement of glucose tolerance.Anandamide (100 ng, ICV bilateral injection, single) partially prevents streptozotocin (STZ)-induced cognitive impairments, changes in synaptic markers and ventricle enlargement.Anandamide exerts anti-inflammatory activities, attenuating the development of inflammation in a mouse model of ulcerative colitis.Anandamide alleviates lipopolysaccharide (LPS)-induced neuroinflammation in rat primary microglial cultures. Animal Model:Male Wistar rats (3-4 months, 350-400 g, STZ-induced AD-like sporadic dementia model) Dosage:100 ng Administration:ICV bilateral injection, single Result:Prevented recognition and non-associative emotional memory impairments induced by STZ, but did not influence tone fear conditioning. Decreased BAG2 (Bcl2-associated athanogene) levels, and prevented STZ-induced ventricle enlargement.

(5Z,8Z,11Z,14Z)-N-(2-Hydroxyethyl)icosa-5,8,11,14-tetraenamide

GPCR/G Protein

Cannabinoid Receptor

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94421-68-8

347.53

C22H37NO2

>98% (HPLC)

In Vitro:?DMSO : ≥ 100 mg/mL (287.74 mM)

CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(NCCO)=O

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(-20℃)

With Ice Pack

≥ 2 years