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. 2021 May 12;179(8):1620–1639. doi: 10.1111/bph.15443

TABLE 2.

Functional abnormalities of ADSHE‐mutant nAChRs

Gene CRHNA4 CRHNB2
Mutation (aminoacid change) c.839C > T (S280F) c.870_872dupGCT (L291dup: insL) c.851C > T (S284L) c.859G > C (V287L)
Cell type Xenopus oocyte Xenopus oocyte Xenopus oocyte HEK293 Xenopus oocyte
ACh sensitivity Enhanced Enhanced Enhanced Enhanced Enhanced
Desensitisation Enhanced No Enhanced Reduced Enhanced
Use‐dependent potentiation Enhanced Enhanced No
Ca2+ permeability Reduced Reduced No No Reduced
Ca2+ dependency Reduced Reduced Reduced Reduced Reduced
CBZ sensitivity (IC50: μM) (wild: 140 μM) Enhanced (51 μM) Enhanced (66 μM) Reduced (296 μM)
Reference IC50 of CBZ to wild‐type α4β2‐nAChR[1] [2–9] [2–4, 8–10] [3, 8–11] [12] [8]

References: 1. Picard et al. (1999); 2. Figl et al. (1998); 3. Bertrand et al. (2002); 4. Bertrand et al. (1998); 5. Weiland et al. (1996); 6. Kuryatov et al. (1997); 7. Moulard et al. (2001); 8. Rodrigues‐Pinguet et al. (2003); 9. Rodrigues‐Pinguet et al. (2005); 10. Steinlein et al. (1997); 11. Matsushima et al. (2002); 12. De Fusco et al. (2000).