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. Author manuscript; available in PMC: 2024 Jan 1.
Published in final edited form as: Int Rev Neurobiol. 2022 Nov 11;168:311–347. doi: 10.1016/bs.irn.2022.10.002

Table 2.

Sex hormone regulation of mGlu receptor synaptic plasticity.

Family Subtype Region Species/Strain Sexes used Sex diff Key findings First author (Year)
Group I mGlu1 HPC Rata Both Y E2 facilitates CREB phosphorylation through ERα/mGlu1, PLC, PKC, and IP3R in ♀ but not ♂ (Boulware et al., 2005) Boulware (2005)
Rat, SD Both (OVX) Y E2 suppresses GABA release probability through ERα/mGlu1, anandamide, and CB1R in ♀ but not ♂ (Huang & Woolley, 2012) Huang (2012)
Rat, SD Both (OVX/CAS) Y E2 suppression of GABA release probability coincides with greater IP3 production in ♀ than ♂. ERα/mGlu1 complexes in exist in ♂ but are only regulated by E2 in ♀ (Tabatadze et al., 2015) Tabatadze (2015)
Rat, SD ♀ (OVX) n.a. E2 increases dendritic spine density through activation of mGlu1 (Peterson et al., 2015) Peterson (2015)
mGlu5 Striatum Rata n.a. E2 facilitates CREB phosphorylation through ERα/mGlu5 and MAPK (Grove-Strawser et al., 2010) Grove-Strawser (2010)
NAC core Rat, SD ♀ (ovx) n.a. E2 decreases dendritic spine density through activation of mGlu5 (Peterson et al., 2015) Peterson (2015)
NAC shell Rat, SD ♂ (CAS) n.a. DHT decreases dendritic spine density in the NAC shell, but not core, through mGlu5 (Gross et al., 2018) Gross (2018)
Group II mGlu2/3 HPC Rata Both Y E2 decreases CREB phosphorylation through mGlu2 and/or mGlu3 inhibition of L-type calcium channels in ♀ but not ♂ (Boulware et al., 2005) Boulware (2005)
mGlu3 Striatum Rata n.a. E2 decreases CREB phosphorylation through mGlu3 inhibition of L-type calcium channels (Grove-Strawser et al., 2010) Grove-Strawser (2010)
a

Pyramidal neurons cultured from P1-P2 rat pups, experiments performed at 9 d.i.v.; strain not specified

CAS, castrated; CB1R, cannabinoid receptor type 1; CREB, cAMP response element-binding protein; DHT, dihydrotestosterone; GABA, gamma-aminobutyric acid; E2, estradiol; ER, estrogen receptor; HPC, hippocampus; IP3R, inositol triphosphate receptor; MAPK, mitogen-activated protein kinase; n.a., not addressed; NAC, nucleus accumbens; OVX, ovariectomized; PLC, phospholipase C; PKC, protein kinase C; SD, Sprague Dawley