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HPLC-Based Activity Profiling for GABAA Receptor Modulators in Searsia pyroides Using a Larval Zebrafish Locomotor Assay.

Authors :
Moradi-Afrapoli F
van der Merwe H
De Mieri M
Wilhelm A
Stadler M
Zietsman PC
Hering S
Swart K
Hamburger M
Source :
Planta medica [Planta Med] 2017 Oct; Vol. 83 (14-15), pp. 1169-1175. Date of Electronic Publication: 2017 May 16.
Publication Year :
2017

Abstract

A dichloromethane extract from leaves of Searsia pyroides potentiated gamma aminobutyric acid-induced chloride currents by 171.8 ± 54% when tested at 100 µg/mL in Xenopus oocytes transiently expressing gamma aminobutyric acid type A receptors composed of α <subscript>1</subscript> β <subscript>2</subscript> γ <subscript>2</subscript> s subunits. In zebrafish larvae, the extract significantly lowered pentylenetetrazol-provoked locomotion when tested at 4 µg/mL. Active compounds of the extract were tracked with the aid of HPLC-based activity profiling utilizing a previously validated zebrafish larval locomotor activity assay. From two active HPLC fractions, compounds 1  -  3 were isolated. Structurally related compounds 4  -  6 were purified from a later eluting inactive HPLC fraction. With the aid of <superscript>1</superscript> H and <superscript>13</superscript> C NMR and high-resolution mass spectrometry, compounds 1  -  6 were identified as analogues of anacardic acid. Compounds 1  -  3 led to a concentration-dependent decrease of pentylenetetrazol-provoked locomotion in the zebrafish larvae model, while 4  -  6 were inactive. Compounds 1  -  3 enhanced gamma aminobutyric acid-induced chloride currents in Xenopus oocytes in a concentration-dependent manner, while 4  -  6 only showed marginal enhancements of gamma aminobutyric acid-induced chloride currents. Compounds 2, 3 , and 5 have not been reported previously.<br />Competing Interests: Conflict of Interest: None.<br /> (Georg Thieme Verlag KG Stuttgart · New York.)

Details

Language :
English
ISSN :
1439-0221
Volume :
83
Issue :
14-15
Database :
MEDLINE
Journal :
Planta medica
Publication Type :
Academic Journal
Accession number :
28511229
Full Text :
https://doi.org/10.1055/s-0043-110768