Hsp90β inhibitors prevent GLT-1 degradation but have no beneficial efficacy on absence epilepsy.

Abstract:

:The loss of glutamate transporter-1 (GLT-1) is associated with temporal lobe epilepsy (TLE). A recent study reported that Hsp90β interacted with GLT-1 and recruited it to 20S proteasome for degradation. Therefore, inhibiting Hsp90β may be a new strategy for treating epilepsy. So far, no studies have shown whether the inhibition of Hsp90β had therapeutic effects on absence epilepsy. Using a model of absence epilepsy, we demonstrated that 17-allylamino-17-demethoxygeldanamycin (17AAG) and Ganetespib (STA9090) had no therapeutic effect. Although this is a negative result, it also has a meaningful exploration value for whether Hsp90 inhibitors have therapeutic effects on other epilepsy types.

journal_name

J Asian Nat Prod Res

authors

Peng YC,Wang S,Zhang Y,Huang LJ,Wang XL,Peng Y

doi

10.1080/10286020.2018.1530989

subject

Has Abstract

pub_date

2019-09-01 00:00:00

pages

905-915

issue

9

eissn

1028-6020

issn

1477-2213

journal_volume

21

pub_type

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