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. 2021 Aug 12;15:100380. doi: 10.1016/j.ynstr.2021.100380

Table 4.

Animal PV neuron alterations under enrichment paradigms.

Species Age during manipulation Age at measurement Sex Experimental paradigm Brain region Method Measure Outcome Reference
Rat (Sprague-Dawley) Early postnatal; adolescent Adolescent MS 4h/day; 500uM TAT2A microinjection into PFC every other day from P31–P39 Prelimbic cortex IHC PV cell density rescued MS-induced decrease [49] Ganguly et al. (2015)
Rat (Sprague-Dawley) Early postnatal Juvenile; adult Oral FLX 10 mg/kg/d from P2–P21 Prelimbic cortex IHC; WFA stain PV cell density no change [113] Mukhopadhyay et al. (2021)
Rat (Wistar) Adult Adult EE 2 months Prelimbic cortex IHC Total PV cell number increased [149] Sampedro-Piquero et al. (2016)
Rat (Sprague-Dawley) Adult Adult FLX 10 mg/kg twice daily IP for 15 days, then brains collected on day 35 Prelimbic cortex IHC PV cell density decreased [160] Song et al. (2019)
Rat (Wistar) Adult Adult SI 21 days; FLX 15 mg/kg/day, CLZ 20 mg/kg/day, or vehicle IP during stress. Prelimbic cortex IHC Total PV cell number decreased by SI in vehicle but not CLZ or FLX treatment [167] Todorovic et al. (2018)
Rat (Sprague-Dawley) Adolescent Adolescent R- or S-ketamine 10 mg/kg IP; sacrifice 30 min later Prelimbic cortex IHC PV cell density Decreased by S-ketamine [186] Yang et al. (2015)
Rat (Sprague-Dawley) Early postnatal; adolescent Adolescent MS 4h/day P2–P20; IL-10 intraventricular infusion from P30–P38. Sacrifice on P40 Prelimbic cortex IHC PV cell density; fraction of PV cells co-expressing NR2A density decreased by MS, rescued by IL-10; fraction increased by MS, rescued by IL-10 [182] Wieck et al. (2013)
Rat (Sprague-Dawley) Juvenile-adolescent Adolescent ♂♀ EE P21–P36 Prelimbic cortex Western blot PV protein content no change [35] do Prado et al. (2015)
Rat (Sprague-Dawley) Early postnatal-adolescent Adolescent ♂♀ MS 4h/day from P2–P20; EE P21–P36 Prelimbic cortex Western blot PV protein content decreased in males [35] do Prado et al. (2015)
Rat (Sprague-Dawley) Early postnatal; adolescent Adolescent MS 4h/day; 500uM TAT2A microinjection into PFC every other day from P31–P39 Infralimbic cortex IHC PV cell density rescued MS-induced decrease [49] Ganguly et al. (2015)
Rat (Sprague-Dawley) Early postnatal Juvenile; adult Oral FLX 10 mg/kg/d from P2–P21 Infralimbic cortex IHC; WFA stain PV cell density no change [113] Mukhopadhyay et al. (2021)
Rat (Wistar) Adult Adult EE 2 months Infralimbic cortex IHC Total PV cell number no change [149] Sampedro-Piquero et al. (2016)
Rat (Sprague-Dawley) Adult Adult FLX 10 mg/kg twice daily IP for 15 days, then brains collected on day 35 Infralimbic cortex IHC PV cell density decreased [160] Song et al. (2019)
Rat (Wistar) Adult Adult SI 21 days; FLX 15 mg/kg/day, CLZ 20 mg/kg/day, or vehicle IP during stress. Infralimbic cortex IHC Total PV cell number decreased by SI in vehicle but not CLZ or FLX treatment [167] Todorovic et al. (2018)
Rat (Sprague-Dawley) Adolescent Adolescent R- or S-ketamine 10 mg/kg IP; sacrifice 30 min later Infralimbic cortex IHC PV cell density no change [186] Yang et al. (2015)
Mouse (C57/BL6) Adult Adult 10 mg/kg/d oral FLX 30 days Infralimbic cortex IHC; WFA stain PV + fraction of PNN + cells no change [77] Karpova et al. (2011)
Rat (Sprague-Dawley) Juvenile-adolescent Adolescent ♂♀ EE P21–P36 Infralimbic cortex Western blot PV protein content no change [35] do Prado et al. (2015)
Rat (Sprague-Dawley) Early postnatal-adolescent Adolescent ♂♀ MS 4h/day from P2–P20; EE P21–P36 Infralimbic cortex Western blot PV protein content decreased in males [35] do Prado et al. (2015)
Rat (Sprague-Dawley) Early postnatal Juvenile; adult Oral FLX 10 mg/kg/d from P2–P21 Cingulate cortex IHC; WFA stain PV cell density no change [113] Mukhopadhyay et al. (2021)
Mouse (C57/BL6) Adolescent-adult Adult Dried bonito broth (10%) intake 53 days Medial Prefrontal cortex IHC PV cell density increased [74] Jargalsaikhan et al. (2017)
Rat (Wistar) Adult Adult SI 21 days; FLX 15 mg/kg/day, CLZ 20 mg/kg/day, or vehicle IP during stress. Medial Prefrontal cortex IHC Total PV cell number decreased by SI in vehicle but not CLZ or FLX treatment [167] Todorovic et al. (2018)
Mouse (C57/BL6) Adult Adult FLX 15 mg/kg/day IP for 3 weeks Medial Frontal cortex IHC and WFA stain PV cell density; PV+/PNN + cell density; PNN + fraction of PV cells decreased (all) [125] Ohira et al. (2013)
Mouse (GAD-GFP) Adult Adult IP injection of 20 mg/kg FLX daily for 2 weeks Medial Prefrontal cortex IHC; WFA stain Total PV cell number; total PV+/PNN + cell number; PV + fraction of PNN + cells; perisomatic PV, synaptophysin, and PV+/synaptophysin + puncta densities on pyramidal cells decreased PV+/PNN + cell number; decreased perisomatic PV+/synaptophysin + puncta [63] Guirado et al., 2014
Rat (Wistar) Juvenile-adult Adult ♂♀ SI 7 weeks with 5 mg/kg/day oral apocynin Prefrontal cortex IHC PV immunoreactivity decreased by SI alone, no change in apocynin alone or SI + apocynin [151] Schiavone et al. (2009)
Rat (Wistar) Adult Adult Ketamine 10 mg/kg IP; brains harvested 0.5 and 2h after Prefrontal cortex IHC PV fluorescence intensity decreased 0.5h but not 2h after ketamine treatment [190] Zhou et al. (2014)
Rat (Wistar) Adult Adult Apocynin 5 mg/kg/day oral for 7 days; ketamine 10 mg/kg IP on day 8; brains harvested 0.5 and 2h after ketamine Prefrontal cortex IHC PV fluorescence intensity decreased by ketamine alone but not apocynin + ketamine [190] Zhou et al. (2014)
Rat (Sprague-Dawley) Early postnatal; adolescent Adolescent MS 4h/day; treatment with COX-2 inhibitor NS-398 (8 mg/kg) every other day IP from P30–P38; LH task P41 Prefrontal cortex Western blot PV protein content increased [97] Lukkes et al. (2017)
Rat (Sprague-Dawley) Early postnatal; adolescent Adolescent MS 4h/day; treatment with COX-2 inhibitor NS-398 (8 mg/kg) every other day IP from P30–P38; LH P41; allowed to witness another rat in task 1 day before they did it. Prefrontal cortex Western blot PV protein content no change [97] Lukkes et al. (2017)
Rat (Wistar) Juvenile-adult Adult ♂♀ SI 7 weeks with 5 mg/kg/day oral apocynin Prefrontal cortex Western blot PV protein content decreased by SI alone, no change in apocynin alone or SI + apocynin [151] Schiavone et al. (2009)
Rat (Sprague-Dawley) Adult Adult IFS 15 min on day 0, then EE 2h/day for 30 days. Brains collected on day 46 Prefrontal cortex Western blot PV protein content IFS reduced PV protein, EE + IFS rescued normal amount. No change for EE alone [164] Sun et al. (2016)
Rat (Wistar) Adult Adult Neuregulin-1 infusion to lateral ventricles same time as ketamine 10 mg/kg IP Prefrontal cortex Western blot PV protein content decreased by ketamine but not ketamine + neuregulin-1 [179] Wang et al. (2014)
Rat (Wistar) Adult Adult Ketamine 10 mg/kg IP; brains harvested 0.5 and 2h after Prefrontal cortex Western blot PV protein content decreased 0.5h but not 2h after ketamine treatment [190] Zhou et al. (2014)
Mouse (C57/BL6) Adult Adult ♂♀ 10 mg/kg ketamine IP; 1 week rest Prefrontal Cortex qPCR PV mRNA expression decreased in males [127] Okine et al. (2020)
Mouse (C57/BL6) Adult Adult ♂♀ 10 mg/kg ketamine IP; 1 week rest; 4 weeks UCMS Prefrontal Cortex qPCR PV mRNA expression decreased in males [127] Okine et al. (2020)
Rat (Wistar) Adult Adult Lurasidone 3 mg/kg/day oral for 5 weeks Prefrontal cortex qPCR PV mRNA expression no change [145] Rossetti et al. (2018)
Rat (Wistar) Adult Adult CMS 7 weeks + lurasidone 3 mg/kg/day oral during last 5 weeks of CMS Prefrontal cortex qPCR PV mRNA expression no change [145] Rossetti et al. (2018)
Mouse (C57/BL6) Adolescent Adolescent ♂♀ 10uM ketamine bath application Frontal Association cortex Electrophysiology PV cell firing frequency 10, 30, and 50 min after ketamine infusion increased after ketamine at injected currents of 50, 100, 150, 200, and 250 pA [120] Ng et al. (2018)
PV-Cre; Ai9-tdTomato Mice (C57/BL6); AAV injection of Cre-GCaMP6f Adolescent Adolescent ♂♀ 8 h RS; 10 mg/kg IP ketamine at 4 and 8 h marks Frontal Association cortex layers 2/3 GCaMP6f signal recording PV cell intracellular calcium (average ΔF/Fo) increased by RS + ketamine vs RS + saline [120] Ng et al. (2018)
Mouse (C57/BL6) Adolescent Adolescent ♂♀ 10 mg/kg IP ketamine or saline, followed by 6h RS for 1, 2, 5, or 7 days Frontal Association cortex layers 2/3 In vivo PV axonal bouton imaging PV bouton elimination, formation, and net change in PV bouton number increased elimination at day 7 RS vs no RS; decreased formation at day 5 and day 7 RS vs RS + ketamine; decreased net change in PV bouton number at day 5 and 7 RS compared to no RS group. [120] Ng et al. (2018)
PV-Cre; Ai9-tdTomato Mice (C57/BL6) Adolescent Adolescent ♂♀ CNO and ketamine 10 mg/kg injection into PV-hM3D or PV hM4D rats, followed by 6h RS, for 2 days Frontal Association cortex layers 2/3 DREADD activation/inhibition of PV cells; Microscopy PV cell dendritic spine elimination rate increased by PV cell inhibition [120] Ng et al. (2018)
PV-Cre; Ai9-tdTomato Mice (C57/BL6) Adolescent Adolescent ♂♀ CNO and ketamine 10 mg/kg injection into PV-hM3D or PV hM4D rats, followed by 6h RS, for 2 days Frontal Association cortex layers 2/3 DREADD activation/inhibition of PV cells; Microscopy PV cell dendritic mushroom, stubby, and thin spine elimination rate increased mushroom spine elimination in PV-inhibited mice [120] Ng et al. (2018)
Rat (Wistar) Adult Adult EE 2 months Cingulate cortex IHC Total PV cell number increased [149] Sampedro-Piquero et al. (2016)
Rat (Wistar) Adult Adult SI 21 days; FLX 15 mg/kg/day, CLZ 20 mg/kg/day, or vehicle IP during stress. Cingulate cortex IHC Total PV cell number decreased by SI, SI + FLX, and SI + CLZ [167] Todorovic et al. (2018)
Rat (Wistar) Adult Adult SI 21 days; FLX 15 mg/kg/day, CLZ 20 mg/kg/day, or vehicle IP during stress. Dorsal Peduncular cortex IHC Total PV cell number decreased by SI in vehicle but not CLZ or FLX txt; increased by CLZ alone vs CLZ + SI [167] Todorovic et al. (2018)
Wnt3a-Cre Mice (C57/BL6 ∗ NZB) Not stated Adolescent ♂♀ EE: running wheel and Enviro-Dri bedding added (timeline not stated) Dentate Gyrus IHC PV cell density no change [4] Anstotz et al. (2018)
Tree Shrew (Tupaia Belangeri) Adult Adult 5 weeks' daily psychosocial conflict; FLX (15 mg/kg/day) or SLV-323 (20 mg/kg/day) oral treatment daily for latter 4 weeks Dentate Gyrus IHC Total PV cell number Decreased by stress; rescued by FLX and by SLV-323 [31] Czeh et al. (2005)
Rat (Wistar) Adolescent-adult Adult FLX 15 mg/kg/day or CLZ 20 mg/kg/day with SI for 3 weeks Dentate Gyrus IHC Total PV cell number decreased by FLX + SI compared to SI [44] Filipović et al. (2017)
Rat (Wistar) Juvenile-adolescent Adult Physical exercise 40 days Dentate Gyrus IHC Total PV cell number no change [58] Gomes da Silva et al., 2010
Rat (Wistar) Adolescent-adult Adult CUS 3 weeks. Anhedonic subgroup given escitalopram (5 mg/kg/day) or vehicle IP for 5 weeks Dentate gyrus hilus and granule cell layer IHC PV cell density no change [69] Holm et al. (2011)
Rat (Long-Evans) Adult Adult Physical exercise 30 min/day for 5 weeks Dentate Gyrus IHC Total PV cell number no change [121] Nguyen et al. (2013)
Rat (Wistar) Adult Adult SI 6 weeks with anhedonic rats given tianeptine 10 mg/kg/day IP for last 3 weeks Dentate Gyrus IHC Total PV cell number increased by tianeptine + SI vs SI alone [136] Peric et al. (2018)
Rat (Wistar) Adult Adult EE 2 months Dentate Gyrus IHC Total PV cell number no change [149] Sampedro-Piquero et al. (2016)
Rat (Wistar) Juvenile Adult EE 40 days Dentate Gyrus IHC PV cell density no change [154] Serra et al. (2020)
Rat (Wistar) Juvenile Adult Exercise 40 days Dentate Gyrus IHC PV cell density increased [154] Serra et al. (2020)
Rat (Sprague-Dawley) Adolescent Adolescent R- or S-ketamine 10 mg/kg IP; sacrifice 30 min later Dentate Gyrus IHC PV cell density decreased by S-ketamine [186] Yang et al. (2015)
Rat (Sprague-Dawley) Early postnatal Juvenile; adult Oral FLX 10 mg/kg/d from P2–P21 Dentate Gyrus IHC; WFA stain Total PV cell number; PNN + fraction of PV cells no change [113] Mukhopadhyay et al. (2021)
Mouse (C57/BL6) Prenatal, early postnatal Early postnatal; juvenile ♂♀ Mothers given oral FLX 11.3 mg/kg/d from GD7-P7 Dentate Gyrus IHC; WHA stain Total PV cell number; PV+/PNN + cell number; PV intensity in PV+/PNN + cells no change [172] Umemori et al. (2015)
PV-TRAP Mouse (C57/BL6) Adult Adult ♂♀ 18 days oral FLX 0.167 mg/ml in 1% saccharine drinking water Dentate Gyrus Electrophysiology 5HT-induced change in PV cell membrane potential decreased (hyperpolarized) [146] Sagi et al. (2020)
PV-TRAP Mouse (C57/BL6) Adult Adult ♂♀ 18 days oral FLX 0.167 mg/ml in 1% saccharine drinking water; 5HT5A receptor antagonist administered Dentate Gyrus Electrophysiology 5HT-induced change in PV cell membrane potential no change [146] Sagi et al. (2020)
PV-Cre Mouse (C57/BL6) Adult Adult ♂♀ 18 days oral FLX 0.167 mg/ml in 1% saccharine drinking water; PV cell-specific 5HT5A receptor KO Dentate Gyrus Electrophysiology 5HT-induced change in PV cell membrane potential no change [146] Sagi et al. (2020)
PV-TRAP Mouse (C57/BL6) Adult Adult ♂♀ 18 days oral FLX 0.167 mg/ml in 1% saccharine drinking water Dentate Gyrus Electrophysiology 5HT-induced PV cell firing frequency decreased [146] Sagi et al. (2020)
PV-Cre Mouse (C57/BL6) Adult Adult ♂♀ 18 days oral FLX 0.167 mg/ml in 1% saccharine drinking water; PV cell-specific 5HT5A receptor KO Dentate Gyrus Electrophysiology 5HT-induced PV cell firing frequency no change [146] Sagi et al. (2020)
PV-TRAP Mouse (C57/BL6) Adult Adult ♂♀ 18 days oral FLX 0.167 mg/ml in 1% saccharine drinking water Dentate Gyrus Electrophysiology 5HT-induced PV cell Kv channel potassium current amplitude decreased [146] Sagi et al. (2020)
PV-Cre Mouse (C57/BL6) Adult Adult ♂♀ 18 days oral FLX 0.167 mg/ml in 1% saccharine drinking water; PV cell-specific 5HT5A receptor KO Dentate Gyrus Electrophysiology 5HT-induced PV cell Kv channel potassium current amplitude no change [146] Sagi et al. (2020)
PV-TRAP Mouse (C57/BL6) Adult Adult ♂♀ 18 days oral FLX 0.167 mg/ml in 1% saccharine drinking water Dentate Gyrus Electrophysiology Change in PV cell Kv channel potassium maximum current amplitude after 200 nM PMA or 200 nM PMA+30uM 5HT bath decreased in FLX-treated but not vehicle-treated mice [146] Sagi et al. (2020)
Tree Shrew (Tupaia Belangeri) Adult Adult 5 weeks' daily psychosocial conflict; FLX (15 mg/kg/day) or SLV-323 (20 mg/kg/day) oral treatment daily for latter 4 weeks CA1 IHC Total PV cell number no change [31] Czeh et al. (2005)
Rat (Wistar) Adolescent-adult Adult FLX 15 mg/kg/day or CLZ 20 mg/kg/day with SI for 3 weeks CA1 IHC Total PV cell number increased by FLX vs vehicle; decreased by FLX + SI, CLZ, and CLZ + SI vs vehicle; decreased by FLX + SI vs FLX [44] Filipović et al. (2017)
Rat (Wistar) Juvenile-adolescent Adult Physical exercise 40 days CA1 IHC Total PV cell number increased [58] Gomes da Silva et al., 2010
Rat (Long-Evans) Adult Adult Physical exercise 30 min/day for 5 weeks CA1 IHC Total PV cell number increased [121] Nguyen et al. (2013)
Rat (Wistar) Adult Adult SI 6 weeks with anhedonic rats given tianeptine 10 mg/kg/day IP for last 3 weeks CA1 IHC Total PV cell number increased by tianeptine and tianeptine + SI vs their vehicle controls [136] Peric et al. (2018)
Rat (Wistar) Adult Adult EE 2 months CA1 IHC Total PV cell number no change [149] Sampedro-Piquero et al. (2016)
Rat (Wistar) Juvenile Adult EE 40 days CA1 IHC PV cell density no change [154] Serra et al. (2020)
Rat (Wistar) Juvenile Adult Exercise 40 days CA1 IHC PV cell density no change [154] Serra et al. (2020)
Rat (Sprague-Dawley) Adolescent Adolescent R- or S-ketamine 10 mg/kg IP; sacrifice 30 min later CA1 IHC PV cell density no change [186] Yang et al. (2015)
Mouse (GAD-GFP) Adult Adult IP injection of 20 mg/kg FLX daily for 2 weeks CA1 IHC; WFA stain Total PV cell number; total PV+/PNN + cell number; PV + fraction of PNN + cells decreased (all) [63] Guirado et al., 2014
Mouse (C57/BL6) Adult Adult 10 mg/kg/d oral FLX 30 days CA1 IHC; WFA stain PV + fraction of PNN + cells decreased [77] Karpova et al. 2011
Rat (Sprague-Dawley) Early postnatal Juvenile; adult Oral FLX 10 mg/kg/d from P2–P21 CA1 IHC; WFA stain PNN + fraction of PV cells; total PV cell number decreased fraction in juveniles [113] Mukhopadhyay et al. (2021)
Mouse (C57/BL6) Prenatal, early postnatal Early postnatal; juvenile ♂♀ Mothers given oral FLX 11.3 mg/kg/d from GD7-P7 CA1 IHC; WHA stain Total PV cell number; PV+/PNN + cell number; PV intensity in PV+/PNN + cells no change [172] Umemori et al. (2015)
Rat (Wistar) Juvenile-adult Adult 8 weeks SI starting at P21, followed by 3 weeks re-isolation or pair housing and oral FLX 6 mg/kg/d or vehicle CA1 IHC PV+/PNN + cell number decreased by FLX overall (net effect of re-isolates and pair housing groups combined) [109] Mikics et al. (2018)
Mouse (C57/BL6) Adult Adult Isoflurane anaesthesia 30 min CA1 IHC FosB intensity in PV + cells increased [5] Antila et al. (2017)
Tree Shrew (Tupaia Belangeri) Adult Adult 5 weeks' daily psychosocial conflict; FLX (15 mg/kg/day) or SLV-323 (20 mg/kg/day) oral treatment daily for latter 4 weeks CA2 IHC Total PV cell number Decreased by stress; rescued by SLV-323 [31] Czeh et al. (2005)
Rat (Wistar) Adolescent-adult Adult FLX 15 mg/kg/day or CLZ 20 mg/kg/day with SI for 3 weeks CA2 IHC Total PV cell number increased by FLX + SI and CLZ + SI vs SI alone [44] Filipović et al. (2017)
Rat (Wistar) Adult Adult SI 6 weeks with anhedonic rats given tianeptine 10 mg/kg/day IP for last 3 weeks CA2 IHC Total PV cell number increased by tianeptine and tianeptine + SI vs their vehicle controls [136] Peric et al. (2018)
Rat (Wistar) Juvenile-adolescent Adult Physical exercise 40 days CA2/3 IHC Total PV cell number increased [58] Gomes da Silva et al., 2010
Rat (Long-Evans) Adult Adult Physical exercise 30 min/day for 5 weeks CA2/3 IHC Total PV cell number increased [121] Nguyen et al. (2013)
Rat (Wistar) Juvenile Adult EE 40 days CA2/3 IHC PV cell density no change [154] Serra et al. (2020)
Rat (Wistar) Juvenile Adult Exercise 40 days CA2/3 IHC PV cell density increased [154] Serra et al. (2020)
Tree Shrew (Tupaia Belangeri) Adult Adult 5 weeks' daily psychosocial conflict; FLX (15 mg/kg/day) or SLV-323 (20 mg/kg/day) oral treatment daily for latter 4 weeks CA3 IHC Total PV cell number Decreased by stress; rescued by SLV-323 [31] Czeh et al. (2005)
PV-Cre mice Adult Adult EE Dorsal CA3b IHC Total PV cell number no change [36] Donato et al. (2013)
Rat (Wistar) Adolescent-adult Adult FLX 15 mg/kg/day or CLZ 20 mg/kg/day with SI for 3 weeks CA3 IHC Total PV cell number increased by FLX + SI and CLZ + SI vs SI alone [44] Filipović et al. (2017)
Mouse (C57/BL6) Adult Adult FLX 10 mg/kg/day SC for 21 days starting at P90 CA3 IHC Total PV cell number no change [56] Godavarthi et al. (2014)
Rat (Wistar) Adult Adult SI 6 weeks with anhedonic rats given tianeptine 10 mg/kg/day IP for last 3 weeks CA3 IHC Total PV cell number increased by tianeptine and tianeptine + SI vs their vehicle controls [136] Peric et al. (2018)
Rat (Wistar) Adult Adult EE 2 months CA3 IHC Total PV cell number no change [149] Sampedro-Piquero et al. (2016)
Rat (Sprague-Dawley) Adolescent Adolescent R- or S-ketamine 10 mg/kg IP; sacrifice 30 min later CA3 IHC PV cell density no change [186] Yang et al. (2015)
Rat (Sprague-Dawley) Early postnatal Juvenile; adult Oral FLX 10 mg/kg/d from P2–P21 CA3 IHC; WFA stain Total PV cell number; PNN + fraction of PV cells decreased fraction in juveniles [113] Mukhopadhyay et al. (2021)
Mouse (C57/BL6) Adult Adult FLX 15 mg/kg/day IP for 3 weeks CA3 IHC; WFA stain PV cell density; PV+/PNN + cell density; PNN + fraction of PV cells decreased PV cell density and PV+/PNN + cell density [125] Ohira et al. (2013)
PV-Cre mice Adult Adult EE Dorsal CA3b IHC fraction of PV cells expressing low amounts of PV increased in basket cells and PV cells overall (not chandelier cells) [36] Donato et al. (2013)
PV-Cre mice Adult Adult EE Dorsal CA3b IHC Inhibitory puncta densities onto PV dendrites increased [36] Donato et al. (2013)
PV-Cre mice Adult Adult EE Dorsal CA3b Chemogenetic activation of PV cells; IHC fraction of PV cells expressing high amounts of PV increased [36] Donato et al. (2013)
Rat (Wistar) Juvenile Adult EE 40 days Subiculum IHC PV cell density no change [154] Serra et al. (2020)
Rat (Wistar) Juvenile Adult Exercise 40 days Subiculum IHC PV cell density increased [154] Serra et al. (2020)
Rat (Wistar) Juvenile Adult EE 40 days Hilus IHC PV cell density no change [154] Serra et al. (2020)
Rat (Wistar) Juvenile Adult Exercise 40 days Hilus IHC PV cell density no change [154] Serra et al. (2020)
PV-TRAP Mouse (C57/BL6) Adult Adult ♂♀ 18 days oral FLX 0.167 mg/ml in 1% saccharine drinking water Subgranular zone IHC 5HT5A + fraction of PV cells no change [146] Sagi et al. (2020)
PV-TRAP Mouse (C57/BL6) Adult Adult ♂♀ 18 days oral FLX 0.167 mg/ml in 1% saccharine drinking water Subgranular zone IHC pKv3.1b + fraction of PV cells increased [146] Sagi et al. (2020)
PV-Cre Mouse (C57/BL6) Adult Adult ♂♀ 18 days oral FLX 0.167 mg/ml in 1% saccharine drinking water; PV cell-specific 5HT5A receptor KO Subgranular zone IHC pKv3.1b + fraction of PV cells no change [146] Sagi et al. (2020)
Mouse (C57/BL6) Adolescent-adult Adult Dried bonito broth (10%) intake 53 days Hippocampus IHC PV cell density increased [74] Jargalsaikhan et al. (2017)
Mouse (GAD-GFP) Adult Adult IP injection of 20 mg/kg FLX daily for 2 weeks Hippocampus IHC; WFA stain Total PV cell number; total PV+/PNN + cell number; PV + fraction of PNN + cells; perisomatic PV and synaptophysin puncta densities on pyramidal cells decreased PV+/PNN + cell number and PV + fraction of PNN + cells [63] Guirado et al., 2014
Rat (Wistar) Juvenile Adult EE 40 days Hippocampus IHC; Western blot PV cell density; PV protein content no change [154] Serra et al. (2020)
Rat (Wistar) Juvenile Adult Exercise 40 days Hippocampus IHC; Western blot PV cell density; PV protein content increased protein and density [154] Serra et al. (2020)
Rat (Wistar) Juvenile-adolescent Adult Physical exercise 40 days Hippocampus Western blot PV protein content increased [58] Gomes da Silva et al., 2010
Rat (Sprague-Dawley) Adolescent-adult Adult Paroxetine 5 mg/kg/day injection for 12 days Hippocampus 2D gel then mass spectrometry proteomics on hippocampus samples PV protein content decreased 1.3-fold [104] McHugh et al. (2009)
Rat (Sprague-Dawley) Adult Adult IFS 15 min on day 0, then EE 2h/day for 30 days. Brains collected on day 46 Hippocampus Western blot PV protein content IFS reduced PV protein, EE + IFS rescued normal amount. No change for EE alone [164] Sun et al. (2016)
Rat (Wistar) Adult Adult Neuregulin-1 infusion to lateral ventricles same time as ketamine 10 mg/kg IP Hippocampus Western blot PV protein content decreased by ketamine but not ketamine + neuregulin-1 [177] Wang et al. (2014)
Rat (Wistar-Kyoto) Adolescent Adolescent 7h/day exposure to roman chamomile essential oil or a-pinene vapors for 14 days Hippocampus qPCR PV mRNA expression increased by roman chamomile and a-pinene [84] Kong et al. (2017)
PV-TRAP Mouse (C57/BL6) Adult Adult ♂♀ 18 days oral FLX 0.167 mg/ml in 1% saccharine drinking water Hippocampus Translating ribosome affinity purification (TRAP) PV cell 5HT5A receptor mRNA no change [146] Sagi et al. (2020)
PV-TRAP Mouse (C57/BL6) Adult Adult ♂♀ 18 days oral FLX 0.167 mg/ml in 1% saccharine drinking water Hippocampus Western blot 5HT5A receptor protein level in membrane-bound fraction of hippocampal lysate increased [146] Sagi et al. (2020)
Rat (Wistar) Adult Adult SI 6 weeks with anhedonic rats given tianeptine 10 mg/kg/day IP for last 3 weeks Dorsal Hippocampus IHC Total PV cell number increased by tianeptine and tianeptine + SI vs their vehicle controls [136] Peric et al. (2018)
Rat (Wistar) Adult Adult Lurasidone 3 mg/kg/day oral for 5 weeks Dorsal Hippocampus qPCR; Western blot PV mRNA expression; PV protein content decreased mRNA [145] Rossetti et al. (2018)
Rat (Wistar) Adult Adult CMS 2 weeks, then anhedonic rats received 5 more weeks CMS + lurasidone 3 mg/kg/day oral Dorsal Hippocampus qPCR; Western blot PV mRNA expression; PV protein content no change [145] Rossetti et al. (2018)
Rat (Wistar) Adult Adult Lurasidone 3 mg/kg/day oral for 5 weeks Ventral Hippocampus qPCR; Western blot PV mRNA expression; PV protein content no change [145] Rossetti et al. (2018)
Rat (Wistar) Adult Adult CMS 2 weeks, then anhedonic rats received 5 more weeks CMS + lurasidone 3 mg/kg/day oral Ventral Hippocampus qPCR; Western blot PV mRNA expression; PV protein content no change [145] Rossetti et al. (2018)
Sprague-Dawley rats Adult Adult Daily FS P65–P74, RS 1hr on P65, P66, P74; VPA IP 300 mg/kg or vehicle P60-74 Ventral Hippocampus IHC Total PV cell number decreased by VPA and VPA + stress at 12 weeks old; decreased by VPA + stress at 16 weeks old [57] Gomes et al. (2019)
Sprague-Dawley rats Adult Adult Daily FS P65–P74, RS 1hr on P65, P66, P74; VPA IP 300 mg/kg or vehicle P60-74 Ventral Hippocampus IHC and WFA stain Total PV/PNN + cell number decreased by VPA and VPA + stress at 12 weeks old; decreased by VPA + stress at 16 weeks old [57] Gomes et al. (2019)
Mouse (C57/BL6) Adult Adult FLX 10 mg/kg/day SC 24 days Basolateral Amygdala IHC Total PV cell number no change [56] Godavarthi et al. (2014)
Mouse (C57/BL6) Adolescent-adult Adult Dried bonito broth (10%) intake 53 days Basolateral Amygdala IHC PV cell density increased [74] Jargalsaikhan et al. (2017)
Rat (Wistar) Adult Adult EE 2 months Basolateral Amygdala IHC Total PV cell number no change [149] Sampedro-Piquero et al. (2016)
Rat (Wistar) Adolescent Adult EE 35 days Basolateral Amygdala IHC Total PV cell number; large and small PV cell number increased total and small PV cell number [173] Urakawa et al. (2013)
Mouse (C57/BL6) Prenatal, early postnatal Early postnatal; juvenile ♂♀ Mothers given oral FLX 11.3 mg/kg/d from GD7-P7 Basolateral Amygdala IHC; WHA stain Total PV cell number; PV+/PNN + cell number; PV intensity in PV+/PNN + cells decreased PV+/PNN + cell number at P17 but not P24; other measures unchanged [172] Umemori et al. (2015)
Mouse (C57/BL6) Adult Adult 10 mg/kg/d oral FLX 30 days Basolateral Amygdala IHC; WFA stain PV + fraction of PNN + cells decreased [77] Karpova et al. (2011)
Rat (Sprague-Dawley) Juvenile Adolescent 1 week EE Basolateral Amygdala IHC; WFA stain c-Fos + proportion of PV cells; WFA + proportion of PV cells; c-Fos + proportion of WFA + PV cells decreased c-Fos + proportion of PV cells; decreased c-Fos + proportion of WFA + PV cells [175] Vazquez-Sanroman et al. (2021)
Rat (Sprague-Dawley) Early postnatal; adolescent Adolescent MS 4h/day from P2–P20; treatment with COX-2 inhibitor NS-398 (8 mg/kg) every other day IP from P30–P38; LH task P41 Basolateral Amygdala Western blot PV protein content no change [97] Lukkes et al. (2017)
Rat (Sprague-Dawley) Early postnatal; adolescent Adolescent MS 4h/day from P2–P20; treatment with COX-2 inhibitor NS-398 (8 mg/kg) every other day IP from P30–P38; LH task P41; allowed to witness another rat in task 1d before they did it. Basolateral Amygdala Western blot PV protein content no change [97] Lukkes et al. (2017)
Rat (Wistar) Adolescent Adult EE 35 days Lateral Amygdala IHC Large and small PV cell number no change [173] Urakawa et al. (2013)
Rat (Sprague-Dawley) Adolescent Adolescent R- or S-ketamine 10 mg/kg IP; sacrifice 30 min later Nucleus Accumbens IHC PV cell density no change [186] Yang et al. (2015)
Rat (Wistar) Juvenile-adult Adult ♂♀ SI + 7 weeks with or without 5 mg/kg/day oral apocynin Nucleus Accumbens IHC PV immunoreactivity decreased by SI alone, no change in apocynin alone or SI + apocynin [151] Schiavone et al. (2009)
Rat (Wistar) Juvenile-adult Adult ♂♀ SI + 7 weeks with or without 5 mg/kg/day oral apocynin Nucleus Accumbens Western blot PV protein content decreased by SI alone, no change in apocynin alone or SI + apocynin [151] Schiavone et al. (2009)
Mouse (C57/BL6) Adolescent Adolescent ♂♀ EE or EE + RS 2 h/d for 7 days Barrel cortex IHC c-Fos + fraction of PV cells increased in both [23] Chen et al. (2018)
Mouse (C57/BL6) Early postnatal Early postnatal, adult ♂♀ EE from late pregnancy until P21 Lateral Striatum IHC and WFA stain High-PV and low-PV cell density; high-PV and low-PV PNN + cell density increased low-PV cell density and low-PV/PNN + cell density in early postnatal and adult mice [124] O'Connor et al. (2019)
Mouse (C57/BL6) Early postnatal Early postnatal, adult ♂♀ EE from late pregnancy until P21 Medial Striatum IHC and WFA stain High-PV and low-PV cell density; high-PV and low-PV PNN + cell density increased low-PV cell density and low-PV/PNN + cell density in adults [124] O'Connor et al. (2019)
Rat (Sprague-Dawley) Early postnatal; adolescent Adolescent MS 4h/day from P2–P20; treatment with COX-2 inhibitor NS-398 (8 mg/kg) every other day IP from P30–P38; LH task P41 Dorsal Raphe Nucleus Western blot PV protein content increased [97] Lukkes et al. (2017)
Rat (Sprague-Dawley) Early postnatal; adolescent Adolescent MS 4h/day from P2–P20; treatment with COX-2 inhibitor NS-398 (8 mg/kg) every other day IP from P30–P38; LH P41; allowed to witness another rat in task 1 day before they did it. Dorsal Raphe Nucleus Western blot PV protein content no change [97] Lukkes et al. (2017)
Mouse (C57/BL6) Adult Adult FLX 15 mg/kg/day IP 3 weeks Thalamic Reticular Nucleus IHC and WFA stain PV cell density; PV+/PNN + cell density; PNN + fraction of PV cells no change [125] Ohira et al. (2013)
Mouse (C57/BL6) Adolescent-adult Adult Dried bonito broth (10%) intake 53 days Superior Colliculus IHC PV cell density increased [74] Jargalsaikhan et al. (2017)
Mouse (C57/BL6) Adult Adult CSD 10 days followed by 20 mg/kg/day FLX IP or vehicle for 14 days Ventral Pallidum Electrophysiology Number of spikes elicited by 100 pA current injection in PV(VP-- > LHb) cells; ratio of excitatory:inhibitory inputs onto PV(VP-- > LHb) cells CSD alone increased number of spikes in resilient and susceptible mice, prevented by FLX; decreased ratio in resilient and FLX-treated mice compared to susceptible [83] Knowl et al. (2017)
Mouse (C57/BL6) Adult Adult CSD 10 days followed by 20 mg/kg/day FLX IP or vehicle for 14 days Ventral Pallidum Electrophysiology Number of spikes elicited by 100 pA current injection in PV(VP-- > VTA) cells; ratio of excitatory:inhibitory inputs onto PV(VP-- > VTA) cells decreased spike number in resilient and FLX (FLX vs. susceptible only) mice but not susceptible; ratio increased in susceptible mice [83] Knowl et al. (2017)

Studies of particular significance are bolded. Mouse and rat life stages were defined as the following: early postnatal: P0-19 (postnatal day 0–19, where day of birth is P0; juvenile: P20-30; adolescent: P31-60; and adult: P61+. Abbreviations: CLZ: clozapine; CNO: clozapine N-oxide; CMS: chronic mild stress; CNO: clozapine N-oxide; CSD: chronic social defeat; CSPG: chondroitin sulfate proteoglycan; CUS: chronic unpredictable stress; DREADD: designer receptor exclusively activated by designer drugs; EE: environmental enrichment; FLX: fluoxetine; IFS: inescapable foot shocks; IHC: immunohistochemistry; IL-10: interleukin-10; IP: intraperitoneal; LHb: lateral habenula; mRNA: messenger ribonucleic acid; MS: maternal separation; qPCR: quantitative polymerase chain reaction; RS: restraint stress; SI: social isolation; SC: subcutaneous; VP: ventral pallidum; VPA: valproic acid; VTA: ventral tegmental area; WFA: Wisteria floribunda agglutinin.