Astragali radix and its main bioactive compounds activate the Nrf2-mediated signaling pathway to induce P-glycoprotein and breast cancer resistance protein.

08:00 EDT 19th September 2018 | BioPortfolio

Summary of "Astragali radix and its main bioactive compounds activate the Nrf2-mediated signaling pathway to induce P-glycoprotein and breast cancer resistance protein."

Astragali radix (Huang Qi, HQ), a well-known Chinese herbal medicine, is widely coadministered with many other drugs for treating diseases. The potential herb-drug interactions (HDIs) possibly occur during the combination therapy. P-glycoprotein (P-gp) and breast cancer resistance protein (BCRP) are the crucial targets that mediate the production of HDIs. We previously observed that HQ and its three main bioactive compounds, including Astragaloside IV (AS-IV), calycosin (CS) and formononetin (FMNT), could significantly induce the expression of P-gp and BCRP in HepG2 cells in vitro. However, their modulations on the function of P-gp and BCRP remain unknown; their impact on these two proteins expression in vivo is not clear; the exact regulatory mechanism has also not yet been explored.


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This article was published in the following journal.

Name: Journal of ethnopharmacology
ISSN: 1872-7573


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Medical and Biotech [MESH] Definitions

Compounds formed by condensation of secologanin with tryptamine resulting in a tetrahydro-beta-carboline which is processed further to a number of bioactive compounds. These are especially found in plants of the APOCYNACEAE; LOGANIACEAE; and RUBIACEAE families.

Compounds that bind to and activate PURINERGIC RECEPTORS.

Compounds that selectively bind to and activate ADENOSINE A2 RECEPTORS.

Compounds bind to and activate ADRENERGIC BETA-2 RECEPTORS.

Compounds that bind to and activate ADRENERGIC BETA-1 RECEPTORS.

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