Cheryl a. Frye

Cheryl a. Frye's AcademicInfluence.com Rankings

Cheryl a. Frye

Psychology

#2479

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#2876

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Behavioral Neuroscience

#16

World Rank

#17

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psychology Degrees

Cheryl a. Frye

Biology

#7415

World Rank

#10335

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Neuroscience

#965

World Rank

#1006

Historical Rank

biology Degrees

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Psychology
Biology

Cheryl a. Frye's Degrees

PhD Neuroscience Stanford University

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Cheryl a. Frye's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

The use of the elevated plus maze as an assay of anxiety-related behavior in rodents (2007) (2160)
Estrous cycle and sex differences in performance on anxiety tasks coincide with increases in hippocampal progesterone and 3α,5α-THP (2000) (421)
A Review and Update of Mechanisms of Estrogen in the Hippocampus and Amygdala for Anxiety and Depression Behavior (2006) (409)
Endocrine Disrupters: A Review of Some Sources, Effects, and Mechanisms of Actions on Behaviour and Neuroendocrine Systems (2012) (372)
Withdrawal from 3α-OH-5α-Pregnan-20-One Using a Pseudopregnancy Model Alters the Kinetics of Hippocampal GABAA-Gated Current and Increases the GABAAReceptor α4 Subunit in Association with Increased Anxiety (1998) (325)
Estrus-associated decrements in a water maze task are limited to acquisition (1995) (282)
Changes in Progesterone Metabolites in the Hippocampus Can Modulate Open Field and Forced Swim Test Behavior of Proestrous Rats (2002) (263)
Ovarian steroids enhance object recognition in naturally cycling and ovariectomized, hormone-primed rats (2006) (248)
Estrogens and progestins enhance spatial learning of intact and ovariectomized rats in the object placement task (2007) (246)
Testosterone increases analgesia, anxiolysis, and cognitive performance of male rats (2001) (244)
ERβ-Selective Estrogen Receptor Modulators Produce Antianxiety Behavior when Administered Systemically to Ovariectomized Rats (2005) (227)
The role of neurosteroids and non-genomic effects of progestins and androgens in mediating sexual receptivity of rodents (2001) (194)
The neurosteroid 3α,5α-THP has antiseizure and possible neuroprotective effects in an animal model of epilepsy (1995) (193)
Responses to Laboratory Psychosocial Stress in Postpartum Women (2001) (179)
Estrogen and/or progesterone administered systemically or to the amygdala can have anxiety-, fear-, and pain-reducing effects in ovariectomized rats. (2004) (168)
Testosterone's analgesic, anxiolytic, and cognitive-enhancing effects may be due in part to actions of its 5alpha-reduced metabolites in the hippocampus. (2004) (167)
Testosterone's anti-anxiety and analgesic effects may be due in part to actions of its 5α-reduced metabolites in the hippocampus (2005) (166)
Progesterone metabolites, effective at the GABAA receptor complex, attenuate pain sensitivity in rats (1994) (164)
Neurosteroids Affect Spatial/Reference, Working, and Long-Term Memory of Female Rats (1995) (162)
Antidepressant effects of ERβ-selective estrogen receptor modulators in the forced swim test (2004) (162)
Behavioral effects of 3α-androstanediol I: modulation of sexual receptivity and promotion of GABA-stimulated chloride flux (1996) (161)
Antianxiety and Antidepressive Behavior Produced by Physiological Estradiol Regimen may be Modulated by Hypothalamic–Pituitary–Adrenal Axis Activity (2005) (156)
Differential effects of antiepileptic drugs on sexual function and hormones in men with epilepsy (2005) (154)
Administration of estrogen receptor beta-specific selective estrogen receptor modulators to the hippocampus decrease anxiety and depressive behavior of ovariectomized rats (2007) (153)
The neurosteroids, progesterone and 3α,5α-THP, enhance sexual motivation, receptivity, and proceptivity in female rats (1998) (151)
Estrous cycle and sex differences in performance on anxiety tasks coincide with increases in hippocampal progesterone and 3alpha,5alpha-THP. (2000) (147)
Depression: reduced number of granule cells in the hippocampus of female, but not male, rats due to prenatal restraint stress (2002) (142)
Effect of prenatal stress and gonadal hormone condition on depressive behaviors of female and male rats (2003) (138)
Estradiol or diarylpropionitrile administration to wild type, but not estrogen receptor beta knockout, mice enhances performance in the object recognition and object placement tasks (2008) (134)
Proestrous compared to diestrous wildtype, but not estrogen receptor beta knockout, mice have better performance in the spontaneous alternation and object recognition tasks and reduced anxiety-like behavior in the elevated plus and mirror maze (2009) (131)
Reduced metabolites mediate neuroprotective effects of progesterone in the adult rat hippocampus. The synthetic progestin medroxyprogesterone acetate (Provera) is not neuroprotective. (2006) (125)
Activation of peripheral mitochondrial benzodiazepine receptors in the hippocampus stimulates allopregnanolone synthesis and produces anxiolytic-like effects in the rat (2000) (125)
Androgen Administration to Aged Male Mice Increases Anti-Anxiety Behavior and Enhances Cognitive Performance (2008) (123)
Seizure exacerbation associated with inhibition of progesterone metabolism (2003) (121)
Hormonal milieu affects tailflick latency in female rats and may be attenuated by access to sucrose (1992) (121)
Estrogen action: A historic perspective on the implications of considering alternative approaches (2010) (118)
Progesterone in Conjunction With Estradiol Has Neuroprotective Effects in an Animal Model of Neurodegeneration (1999) (118)
Diet and estrous cycle influence pain sensitivity in rats (1993) (118)
ERβ-selective SERMs produce mnemonic-enhancing effects in the inhibitory avoidance and water maze tasks (2006) (118)
Progesterone enhances motor, anxiolytic, analgesic, and antidepressive behavior of wild-type mice, but not those deficient in type 1 5α-reductase (2004) (117)
Neurosteroidogenesis Today: Novel Targets for Neuroactive Steroid Synthesis and Action and Their Relevance for Translational Research (2016) (116)
Chronic estradiol replacement to aged female rats reduces anxiety-like and depression-like behavior and enhances cognitive performance (2009) (115)
Steroid withdrawal in the mouse results in anxiogenic effects of 3α,5β-THP: a possible model of premenstrual dysphoric disorder (2006) (110)
Androgens with activity at estrogen receptor beta have anxiolytic and cognitive-enhancing effects in male rats and mice (2008) (109)
Estradiol or diarylpropionitrile decrease anxiety-like behavior of wildtype, but not estrogen receptor beta knockout, mice. (2008) (109)
Estrous cycle, pregnancy, and parity enhance performance of rats in object recognition or object placement tasks. (2008) (109)
Anti-seizure effects of progesterone and 3α,5α-THP in kainic acid and perforant pathway models of epilepsy (2000) (106)
Withdrawal from 3alpha-OH-5alpha-pregnan-20-One using a pseudopregnancy model alters the kinetics of hippocampal GABAA-gated current and increases the GABAA receptor alpha4 subunit in association with increased anxiety. (1998) (105)
ANDROGENIC NEUROSTEROIDS: ANTI-SEIZURE EFFECTS IN AN ANIMAL MODEL OF EPILEPSY (1998) (103)
Seizure Activity Is Increased in Endocrine States Characterized by Decline in Endogenous Levels of the Neurosteroid 3α,5α-THP (1998) (102)
Mnemonic effects of testosterone and its 5α-reduced metabolites in the conditioned fear and inhibitory avoidance tasks (2004) (101)
The nucleus accumbens as a site of action for rewarding properties of testosterone and its 5α-reduced metabolites (2002) (101)
Differential Effects of Antiepileptic Drugs on Sexual Function and Reproductive Hormones in Men with Epilepsy: Interim Analysis of a Comparison between Lamotrigine and Enzyme‐inducing Antiepileptic Drugs (2004) (99)
Progestins influence motivation, reward, conditioning, stress, and/or response to drugs of abuse (2007) (97)
Testosterone's metabolism in the hippocampus may mediate its anti-anxiety effects in male rats (2004) (97)
Social isolation stress during the third week of life has age-dependent effects on spatial learning in rats (2002) (96)
Sex differences in salivary cortisol in response to acute stressors among healthy participants, in recreational or pathological gamblers, and in those with posttraumatic stress disorder (2010) (94)
Self-reported dietary restraint is associated with elevated levels of salivary cortisol (2002) (94)
Behavioral effects of 3a-androstanediol II: Hypothalamic and preoptic area actions via a GABAergic mechanism (1996) (93)
The testosterone metabolite and neurosteroid 3α-androstanediol may mediate the effects of testosterone on conditioned place preference (2001) (92)
The Role of Neurosteroids and Nongenomic Effects of Progestins in the Ventral Tegmental Area in Mediating Sexual Receptivity of Rodents (2001) (92)
5α-reduced androgens may have actions in the hippocampus to enhance cognitive performance of male rats (2004) (92)
Allopregnanolone Levels and Symptom Improvement in Severe Premenstrual Syndrome (2002) (91)
Estradiol reduces anxiety- and depression-like behavior of aged female mice (2010) (91)
Progesterone Reduces Pentylenetetrazol‐Induced Ictal Activity of Wild‐Type Mice But Not Those Deficient in Type I 5α‐Reductase (2002) (85)
Neonatal isolation alters stress hormone and mesolimbic dopamine release in juvenile rats (2002) (84)
Posttraining androgens’ enhancement of cognitive performance is temporally distinct from androgens’ increases in affective behavior (2001) (84)
Evidence for a non-genomic action of progestins on sexual receptivity in hamster ventral tegmental area but not hypothalamus (1992) (84)
Androgens’ effects to enhance learning may be mediated in part through actions at estrogen receptor-β in the hippocampus (2007) (84)
3α-hydroxy-5α-pregnan-20-one in the midbrain ventral tegmental area mediates social, sexual, and affective behaviors (2006) (82)
Hippocampal 3α,5α-THP may alter depressive behavior of pregnant and lactating rats (2004) (82)
Intrahippocampal administration of an androgen receptor antagonist, flutamide, can increase anxiety-like behavior in intact and DHT-replaced male rats (2006) (81)
Depression-like behavior of aged male and female mice is ameliorated with administration of testosterone or its metabolites (2009) (80)
Inhibiting progesterone metabolism in the hippocampus of rats in behavioral estrus decreases anxiolytic behaviors and enhances exploratory and antinociceptive behaviors (2001) (80)
Sexual experience of male rats influences anxiety-like behavior and androgen levels (2007) (78)
Inhibiting 5α-reductase in the amygdala attenuates antianxiety and antidepressive behavior of naturally receptive and hormone-primed ovariectomized rats (2006) (77)
Effects of progesterone administration and APPswe+PSEN1Δe9 mutation for cognitive performance of mid-aged mice (2008) (76)
The Neurosteroids DHEA and DHEAS May Influence Cognitive Performance by Altering Affective State (1999) (75)
Neurosteroids’ effects and mechanisms for social, cognitive, emotional, and physical functions (2009) (75)
Enhancing effects of estrogen on inhibitory avoidance performance may be in part independent of intracellular estrogen receptors in the hippocampus (2002) (75)
Gonadal, adrenal, and neuroactive steroids' role in ictal activity (2004) (74)
Estradiol to aged female or male mice improves learning in inhibitory avoidance and water maze tasks (2005) (74)
Finasteride Blocks the Reduction in Ictal Activity Produced by Exogenous Estrous Cyclicity (1998) (74)
Progesterone has rapid and membrane effects in the facilitation of female mouse sexual behavior (1999) (73)
Progestins Can Have a Membrane-Mediated Action in Rat Midbrain for Facilitation of Sexual Receptivity (1996) (73)
Cyclic Withdrawal From Endogenous and Exogenous Progesterone Increases Kainic Acid and Perforant Pathway Induced Seizures (1999) (72)
Effects of paced and non-paced mating stimulation on plasma progesterone, 3α-diol and corticosterone (1996) (72)
An overview of oral contraceptives (2006) (71)
Antidepressant effects of ERbeta-selective estrogen receptor modulators in the forced swim test. (2004) (71)
The nitric oxide synthase inhibitor 7-nitroindazole displays enhanced anxiolytic efficacy without tolerance in rats following subchronic administration (1998) (71)
Genomic and Non-genomic Actions of Progesterone in the Control of Female Hamster Sexual Behavior (1994) (70)
The testosterone metabolite and neurosteroid 3α-androstanediol may mediate the effects of testosterone on conditioned place preference (2001) (69)
Influence of time of mating and paced copulation on induction of pseudopregnancy in cyclic female rats. (1990) (69)
Estrogen has mnemonic-enhancing effects in the inhibitory avoidance task (2004) (68)
Estradiol decreases anxiety behavior and enhances inhibitory avoidance and gestational stress produces opposite effects (2007) (67)
Progestogens and estrogen influence impulsive burying and avoidant freezing behavior of naturally cycling and ovariectomized rats (2009) (66)
Antisense Oligodeoxynucleotides for Estrogen Receptor-β and α Attenuate Estradiol's Modulation of Affective and Sexual Behavior, Respectively (2008) (63)
Endogenous levels of 5 alpha-reduced progestins and androgens in fetal vs. adult rat brains. (1999) (62)
Rapid and estrogen receptor beta mediated actions in the hippocampus mediate some functional effects of estrogen (2008) (62)
Prenatal stress reduces the effectiveness of the neurosteroid 3α,5α‐THP to block kainic‐acid‐induced seizures (1999) (62)
Progesterone to ovariectomized mice enhances cognitive performance in the spontaneous alternation, object recognition, but not placement, water maze, and contextual and cued conditioned fear tasks (2008) (62)
Gambling pathology is associated with dampened cortisol response among men and women (2010) (61)
Progesterone’s effects to reduce anxiety behavior of aged mice do not require actions via intracellular progestin receptors (2006) (61)
Some rewarding effects of androgens may be mediated by actions of its 5α-reduced metabolite 3α-androstanediol (2007) (58)
Steroid withdrawal in the mouse results in anxiogenic effects of 3alpha,5beta-THP: a possible model of premenstrual dysphoric disorder. (2006) (57)
GABAA, D1, and D5, but not progestin receptor, antagonist and anti-sense oligonucleotide infusions to the ventral tegmental area of cycling rats and hamsters attenuate lordosis (1999) (57)
Chronic administration of androgens with actions at estrogen receptor beta have anti-anxiety and cognitive-enhancing effects in male rats (2009) (57)
Engaging in paced mating, but neither exploratory, anti-anxiety, nor social behavior, increases 5alpha-reduced progestin concentrations in midbrain, hippocampus, striatum, and cortex. (2007) (57)
3α-Androstanediol, but Not Testosterone, Attenuates Age-Related Decrements in Cognitive, Anxiety, and Depressive Behavior of Male Rats (2009) (57)
Ventral Tegmental Area Infusions of Inhibitors of the Biosynthesis and Metabolism of 3α,5α‐THP Attenuate Lordosis of Hormone‐Primed and Behavioural Oestrous Rats and Hamsters (2001) (57)
Immune stress in late pregnant rats decreases length of gestation and fecundity, and alters later cognitive and affective behaviour of surviving pre-adolescent offspring (2011) (56)
Communication, interventions, and scientific advances in autism: A commentary (2010) (56)
Infusions of 5α‐Pregnan‐3α‐Ol‐20‐One (3α,5α‐THP) to the Ventral Tegmental Area, but not the Substantia Nigra, Enhance Exploratory, Anti‐Anxiety, Social and Sexual Behaviours and Concomitantly Increase 3α,5α‐THP Concentrations in the Hippocampus, Diencephalon and Cortex of Ovariectomised Oestrogen‐Pr (2006) (56)
Analgesic effects of the neurosteroid 3α-androstanediol (1996) (55)
Estradiol benzoate potentiates neuroactive steroids' effects on pain sensitivity (1996) (55)
Differences in affective behaviors and hippocampal allopregnanolone levels in adult rats of lines selectively bred for infantile vocalizations (2005) (54)
Progesterone enhances performance of aged mice in cortical or hippocampal tasks (2008) (54)
Estrogen-priming can enhance progesterone's anti-seizure effects in part by increasing hippocampal levels of allopregnanolone (2005) (54)
Chronic anabolic-androgenic steroid treatment affects brain GABA(A) receptor-gated chloride ion transport. (1996) (54)
3α-OH-DHP and 5α-THDOC implants to the ventral tegmental area facilitate sexual receptivity in hamsters after progesterone priming to the ventral medial hypothalamus (1993) (53)
Progesterone and 3 alpha-androstanediol conjugated to bovine serum albumin affects estrous behavior when applied to the MBH and POA. (1996) (52)
Hormonal influences on seizures: basic neurobiology. (2008) (50)
Milestones on Steroids and the Nervous System: 10 Years of Basic and Translational Research (2012) (50)
Bicuculline infused into the hamster ventral tegmentum inhibits, while sodium valproate facilitates, sexual receptivity (1993) (50)
Androgens in the hippocampus can alter, and be altered by, ictal activity (2004) (48)
Androgens Are Neuroprotective in the Dentate Gyrus of Adrenalectomized Female Rats (2000) (47)
Central allopregnanolone is increased in rat pups in response to repeated, short episodes of neonatal isolation. (2000) (47)
Muscimol facilitates sexual receptivity in hamsters when infused into the ventral tegmentum (1992) (47)
Testosterone reduces pentylenetetrazole-induced ictal activity of wildtype mice but not those deficient in type I 5α-reductase (2001) (46)
Corticosteroid and neurosteroid dysregulation in an animal model of autism, BTBR mice (2010) (46)
Mid-aged and aged wild-type and progestin receptor knockout (PRKO) mice demonstrate rapid progesterone and 3α,5α-THP-facilitated lordosis (2006) (46)
Progestins influence performance on cognitive tasks independent of changes in affective behavior (2000) (45)
Effects of two estradiol regimens on anxiety and depressive behaviors and trophic effects in peripheral tissues in a rodent model. (2009) (45)
Steroids, reproductive endocrine function, and affect. A review. (2009) (45)
3α,5α-THP: a potential plasma neurosteroid biomarker in Alzheimer's disease and perhaps non-Alzheimer's dementia (2006) (44)
Menstrual cycle and sex differences influence salt preference (1994) (44)
The neurosteroid, 3α-androstanediol, prevents inhibitory avoidance deficits and pyknotic cells in the granule layer of the dentate gyrus induced by adrenalectomy in rats (2000) (44)
P-3-BSA, but not P-11-BSA, implants in the VTA rapidly facilitate receptivity in hamsters after progesterone priming to the VMH (1993) (43)
5α-reduced progesterone metabolites are essential in hamster VTA for sexual receptivity (1994) (43)
Prenatal Stress Alters Reproductive Responses of Rats in Behavioral Estrus and Paced Mating of Hormone-Primed Rats (2002) (42)
Novel receptor targets for production and action of allopregnanolone in the central nervous system: a focus on pregnane xenobiotic receptor (2014) (41)
Anti-nociception following exposure to trimethylthiazoline, peripheral or intra-amygdala estrogen and/or progesterone (2003) (41)
Effects and Mechanisms of 3α,5α,-THP on Emotion, Motivation, and Reward Functions Involving Pregnane Xenobiotic Receptor (2011) (41)
Anti-sense oligonucleotides, for progestin receptors in the VMH and glutamic acid decarboxylase in the VTA, attenuate progesterone-induced lordosis in hamsters and rats (2000) (41)
Juvenile offspring of rats exposed to restraint stress in late gestation have impaired cognitive performance and dysregulated progestogen formation (2011) (41)
Menstrual cycle and dietary restraint influence taste preferences in young women (1994) (40)
Progestins' actions in the VTA to facilitate lordosis involve dopamine-like type 1 and 2 receptors (2004) (39)
The neurosteroids, progesterone and 3alpha,5alpha-THP, enhance sexual motivation, receptivity, and proceptivity in female rats. (1998) (39)
Allopregnanolone levels and seizure frequency in progesterone-treated women with epilepsy (2014) (39)
Progesterone and the neural mechanisms of hamster sexual behavior (1994) (38)
Type 1 5α-reductase may be required for estrous cycle changes in affective behaviors of female mice (2012) (37)
Women with PTSD have lower basal salivary cortisol levels later in the day than do men with PTSD: A preliminary study (2010) (37)
Olanzapine’s effects to reduce fear and anxiety and enhance social interactions coincide with increased progestin concentrations of ovariectomized rats (2003) (36)
Testosterone enhances aggression of wild-type mice but not those deficient in type I 5α-reductase (2002) (36)
Progesterone enhances learning and memory of aged wildtype and progestin receptor knockout mice (2010) (35)
Conjugated equine estrogen enhances rats' cognitive, anxiety, and social behavior (2008) (35)
Membrane actions of progestins at dopamine type 1-like and GABAA receptors involve downstream signal transduction pathways (2008) (35)
Progestin Concentrations Are Increased following Paced Mating in Midbrain, Hippocampus, Diencephalon, and Cortex of Rats in Behavioral Estrus, but Only in Midbrain of Diestrous Rats (2006) (35)
Chapter 3 Hormonal Influences on Seizures (2008) (35)
Estradiol-Induced Conditioned Place Preference may Require Actions at Estrogen Receptors in the Nucleus Accumbens (2007) (35)
Differential Effects of Antiepileptic Drugs on Neuroactive Steroids in Men with Epilepsy (2006) (35)
Progestins in the Hippocampus of Female Rats Have Antiseizure Effects in a Pentylenetetrazole Seizure Model (2004) (34)
II. Cognitive performance of middle-aged female rats is influenced by capacity to metabolize progesterone in the prefrontal cortex and hippocampus (2011) (34)
Androgens’ performance-enhancing effects in the inhibitory avoidance and water maze tasks may involve actions at intracellular androgen receptors in the dorsal hippocampus (2007) (34)
Infusions of 3α,5α-THP to the VTA enhance exploratory, anti-anxiety, social, and sexual behavior and increase levels of 3α,5α-THP in midbrain, hippocampus, diencephalon, and cortex of female rats (2008) (34)
Inhibiting Biosynthesis and/or Metabolism of Progestins in the Ventral Tegmental Area Attenuates Lordosis of Rats in Behavioural Oestrus (2005) (33)
Parity and estrogen-administration alter affective behavior of ovariectomized rats (2008) (33)
Lordosis of Rats Is Modified by Neurosteroidogenic Effects of Membrane Benzodiazepine Receptors in the Ventral Tegmental Area (2003) (32)
3α,5α-THP in the midbrain ventral tegmental area of rats and hamsters is increased in exogenous hormonal states associated with estrous cyclicity and sexual receptivity (1999) (32)
Intravenous progesterone elicits a more rapid induction of lordosis in rats than does SKF38393 (2000) (32)
Inhibition of 5α‐Reductase Activity in Late Pregnancy Decreases Gestational Length and Fecundity and Impairs Object Memory and Central Progestogen Milieu of Juvenile Rat Offspring (2011) (32)
The neurosteroid 3 alpha, 5 apha-THP has antiseizure and possible neuroprotective effects in an animal model of epilepsy. (1995) (32)
Some rewarding effects of androgens may be mediated by actions of its 5alpha-reduced metabolite 3alpha-androstanediol. (2007) (30)
Raloxifene and/or estradiol decrease anxiety-like and depressive-like behavior, whereas only estradiol increases carcinogen-induced tumorigenesis and uterine proliferation among ovariectomized rats (2010) (30)
Exploratory, anti-anxiety, social, and sexual behaviors of rats in behavioral estrus is attenuated with inhibition of 3α,5α-THP formation in the midbrain ventral tegmental area (2008) (30)
Infusion of 3α,5α-THP to the pontine reticular formation attenuates PTZ-induced seizures (2000) (30)
Inhibition of 5alpha-reductase enzyme or GABA(A) receptors in the VMH and the VTA attenuates progesterone-induced sexual behavior in rats and hamsters. (2001) (30)
Increasing 3alpha,5alpha-THP following inhibition of neurosteroid biosynthesis in the ventral tegmental area reinstates anti-anxiety, social, and sexual behavior of naturally receptive rats. (2009) (29)
Anti-seizure effects of progesterone and 3alpha,5alpha-THP in kainic acid and perforant pathway models of epilepsy. (2000) (28)
Antisense oligodeoxynucleotides for estrogen receptor-beta and alpha attenuate estradiol's modulation of affective and sexual behavior, respectively. (2008) (28)
Progesterone, compared to medroxyprogesterone acetate, to C57BL/6, but not 5α-reductase mutant, mice enhances object recognition and placement memory and is associated with higher BDNF levels in the hippocampus and cortex (2013) (28)
Perforant path stimulation in rats produces seizures, loss of hippocampal neurons, and a deficit in spatial mapping which are reduced by prior MK-801 (2000) (28)
Fluoxetine May Influence Lordosis of Rats through Effects on Midbrain 3α,5α‐THP Concentrations (2003) (28)
Prenatal stress produces deficits in socio-sexual behavior of cycling, but not hormone-primed, Long–Evans rats (2002) (28)
Effects and mechanisms of progestogens and androgens in ictal activity (2010) (28)
Hippocampal 3alpha,5alpha-THP may alter depressive behavior of pregnant and lactating rats. (2004) (28)
Mitochondrial Benzodiazepine Receptors in the Ventral Tegmental Area Modulate Sexual Behaviour of Cycling or Hormone‐Primed Hamsters (2003) (28)
Prenatal stress reduces the effectiveness of the neurosteroid 3 alpha,5 alpha-THP to block kainic-acid-induced seizures. (1999) (27)
In the Ventral Tegmental Area, G-Proteins and cAMP Mediate the Neurosteroid 3α,5α-THP’s Actions at Dopamine Type 1 Receptors for Lordosis of Rats (2005) (26)
Brain Levels of Prostaglandins, Endocannabinoids, and Related Lipids Are Affected by Mating Strategies (2013) (26)
Progesterone and 3α,5α-THP enhance sexual receptivity in mice. (2001) (26)
Endocrine disrupting chemicals and ovulation: Is there a relationship? (2016) (26)
Administration of estrogen to ovariectomized rats promotes conditioned place preference and produces moderate levels of estrogen in the nucleus accumbens (2006) (26)
Novel Substrates for, and Sources of, Progestogens for Reproduction (2011) (26)
3α,5α-THP mediates progestins' effects to protect against adrenalectomy-induced cell death in the dentate gyrus of female and male rats (2004) (26)
Taste preferences and sensory perceptions in female varsity swimmers (1995) (25)
Progesterone-facilitated lordosis of estradiol-primed mice is attenuated by knocking down expression of membrane progestin receptors in the midbrain (2014) (25)
Strain and sex based characterization of behavioral expressions in non-induced compulsive-like mice (2017) (25)
Gestational exposure to variable stressors produces decrements in cognitive and neural development of juvenile male and female rats. (2011) (25)
Progestin-facilitated lordosis of hamsters may involve dopamine-like type 1 receptors in the ventral tegmental area (2005) (24)
Neurosteroids – From Basic Research to Clinical Perspectives (2009) (24)
Gestational or acute restraint in adulthood reduces levels of 5α-reduced testosterone metabolites in the hippocampus and produces behavioral inhibition of adult male rats (2012) (24)
Role of androgens in epilepsy (2006) (24)
Actions at GABAA receptors in the hippocampus may mediate some antiseizure effects of progestins (2005) (24)
Progesterone attenuates depressive behavior of younger and older adult C57/BL6, wildtype, and progesterone receptor knockout mice (2011) (24)
Divergent mechanisms for trophic actions of estrogens in the brain and peripheral tissues (2011) (23)
Progesterone can enhance consolidation and/or performance in spatial, object and working memory tasks in Long–Evans rats (2009) (23)
Progesterone reduces depression-like behavior in a murine model of Alzheimer’s Disease (2009) (23)
Seizure activity is increased in endocrine states characterized by decline in endogenous levels of the neurosteroid 3 alpha,5 alpha-THP. (1998) (22)
Salivary alpha‐amylase and cortisol among pentecostals on a worship and nonworship day (2010) (22)
Involvement of pregnane xenobiotic receptor in mating-induced allopregnanolone formation in the midbrain and hippocampus and brain-derived neurotrophic factor in the hippocampus among female rats (2014) (22)
Mnemonic effects of progesterone to mice require formation of 3α,5α-THP (2010) (22)
Self-administration of 3α-androstanediol increases locomotion and analgesia and decreases aggressive behavior of male hamsters (2007) (22)
Attenuating 5α-pregnane-3α-ol-20-one formation in the hippocampus of female rats increases pentylenetetrazole-induced seizures (2005) (22)
3alpha-hydroxy-5alpha-pregnan-20-one in the midbrain ventral tegmental area mediates social, sexual, and affective behaviors. (2006) (21)
Low doses of cocaine decrease, and high doses increase, anxiety-like behavior and brain progestogen levels among intact rats (2010) (21)
Estradiol tends to improve inhibitory avoidance performance in adrenalectomized male rats and reduces pyknotic cells in the dentate gyrus of adrenalectomized male and female rats (2001) (21)
Mid-aged and aged wild-type and progestin receptor knockout (PRKO) mice demonstrate rapid progesterone and 3alpha,5alpha-THP-facilitated lordosis. (2006) (21)
In the ventral tegmental area picrotoxin blocks FGIN 1-27-induced increases in sexual behavior of rats and hamsters (2005) (21)
Progesterone turnover to its 5α-reduced metabolites in the ventral tegmental area of the midbrain is essential for initiating social and affective behavior and progesterone metabolism in female rats (2010) (21)
Early postnatal stimulation alters pregnane neurosteroids in the hippocampus (2006) (21)
Progesterone and allopregnanolone are induced by cocaine in serum and brain tissues of male and female rats (2008) (20)
In the ventral tegmental area, progestins have actions at D1 receptors for lordosis of hamsters and rats that involve GABAA receptors (2006) (20)
Membrane progestin receptors in the midbrain ventral tegmental area are required for progesterone-facilitated lordosis of rats (2013) (20)
Male gamblers have significantly greater salivary cortisol before and after betting on a horse race, than do female gamblers (2010) (19)
MK-801 infusions to the ventral tegmental area and ventromedial hypothalamus produce opposite effects on lordosis of hormone-primed rats (2007) (19)
Infusions of bicuculline to the ventral tegmental area attenuates sexual, exploratory, and anti-anxiety behavior of proestrous rats (2009) (19)
Allopregnanolone levels before and after selective serotonin reuptake inhibitor treatment of premenstrual symptoms. (2009) (19)
Zaprinast, a Phosphodiesterase 5 Inhibitor, Overcomes Sexual Dysfunction Produced by Fluoxetine, a Selective Serotonin Reuptake Inhibitor in Hamsters (2003) (18)
Progesterone facilitates exploration, affective and social behaviors among wildtype, but not 5α-reductase Type 1 mutant, mice (2013) (18)
In the Ventral Tegmental Area, Cyclic AMP Mediates the Actions of Progesterone at Dopamine Type 1 Receptors for Lordosis of Rats and Hamsters (2006) (17)
Progestins’ effects on sexual behaviour of female rats and hamsters involving D1 and GABAA receptors in the ventral tegmental area may be G-protein-dependent (2006) (17)
Neurosteroids for a successful pregnancy (2011) (17)
Progesterone reduces hyperactivity of female and male dopamine transporter knockout mice (2010) (17)
Estrogen increases latencies to seizures and levels of 5α-pregnan-3α-ol-20-one in hippocampus of wild-type, but not 5α-reductase knockout, mice (2009) (17)
Motivated behaviors and levels of 3α,5α-THP in the midbrain are attenuated by knocking down expression of pregnane xenobiotic receptor in the midbrain ventral tegmental area of proestrous rats. (2013) (16)
Infusions of 5alpha-pregnan-3alpha-ol-20-one (3alpha,5alpha-THP) to the ventral tegmental area, but not the substantia nigra, enhance exploratory, anti-anxiety, social and sexual behaviours and concomitantly increase 3alpha,5alpha-THP concentrations in the hippocampus, diencephalon and cortex of ova (2006) (16)
Estrogen is necessary for 5α-pregnan-3α-ol-20-one (3α,5α-THP) infusion to the ventral tegmental area to facilitate social and sexual, but neither exploratory nor affective behavior of ovariectomized rats (2008) (16)
Progesterone reduces depressive behavior of young ovariectomized, aged progestin receptor knockout, and aged wild type mice in the tail suspension test (2011) (15)
Nociceptive and anxiety-like behavior in reproductively competent and reproductively senescent middle-aged rats. (2009) (15)
Endocrine-disrupting chemicals: elucidating our understanding of their role in sex and gender-relevant end points. (2014) (15)
The pregnane xenobiotic receptor, a prominent liver factor, has actions in the midbrain for neurosteroid synthesis and behavioral/neural plasticity of female rats (2014) (15)
Steroids, reproductive endocrine function, and cognition. A review. (2009) (15)
3alpha,5alpha-THP: a potential plasma neurosteroid biomarker in Alzheimer's disease and perhaps non-Alzheimer's dementia. (2006) (15)
Urine cortisol concentration as a biomarker of stress is unrelated to IVF outcomes in women and men (2014) (15)
Prenatal Stress Alters Progestogens to Mediate Susceptibility to Sex-Typical, Stress-Sensitive Disorders, such as Drug Abuse: A Review (2011) (15)
Effects of olanzapine infusions to the ventral tegmental area on lordosis and midbrain 3α,5α-THP concentrations in rats (2003) (14)
Conjugated equine estrogen, with medroxyprogesterone acetate, enhances formation of 5α-reduced progestogens and reduces anxiety-like behavior of middle-aged rats (2010) (14)
Progesterone's 5α-reduced metabolite, 3α,5α-THP, mediates lateral displacement of hamsters (2005) (14)
Fluoxetine-induced decrements in sexual responses of female rats and hamsters are reversed by 3α,5α-THP. (2010) (14)
Oestrogen effects in olivo-cerebellar and hippocampal circuits. (2000) (14)
Progestin facilitation of lordosis in rodents involves adenylyl cyclase activity in the ventral tegmental area (2006) (14)
Progesterone, administered before kainic acid, prevents decrements in cognitive performance in the Morris Water Maze (2011) (14)
Antiseizure effects of 3α-androstanediol and/or 17β-estradiol may involve actions at estrogen receptor β (2009) (14)
Neurochemical and behavioral effects of chronic unpredictable stress (2014) (14)
Activity of protein kinase C is important for 3α,5α-THP's actions at dopamine type 1-like and/or GABAA receptors in the ventral tegmental area for lordosis of rats (2008) (13)
In the ventral tegmental area, G-proteins mediate progesterone’s actions at dopamine type 1 receptors for lordosis of rats and hamsters (2006) (13)
The Steroidogenesis Inhibitor Finasteride Reduces the Response to Both Stressful and Rewarding Stimuli (2019) (13)
Fluoxetine may influence lordosis of rats through effects on midbrain 3 alpha,5 alpha-THP concentrations. (2003) (12)
Ketogenic diet decreases circulating concentrations of neuroactive steroids of female rats (2005) (12)
Effects of neurosteroid actions at N-methyl-d-aspartate and GABAA receptors in the midbrain ventral tegmental area for anxiety-like and mating behavior of female rats (2010) (12)
Female mice with deletion of Type One 5α-reductase have reduced reproductive responding during proestrus and after hormone-priming (2014) (12)
Infusions of anti-sense oligonucleotides for DARPP-32 to the ventral tegmental area reduce effects of progesterone- and a dopamine type 1-like receptor agonist to facilitate lordosis (2010) (11)
In the Ventral Tegmental Area, the Membrane‐Mediated Actions of Progestins for Lordosis of Hormone‐Primed Hamsters Involve Phospholipase C and Protein Kinase C (2007) (11)
I. Levels of 5α-reduced progesterone metabolite in the midbrain account for variability in reproductive behavior of middle-aged female rats (2011) (11)
Research Brief: Self-Reports of a Constellation of Persistent Antiandrogenic, Estrogenic, Physical, and Psychological Effects of Finasteride Usage Among Men (2018) (10)
Progestogens’ effects and mechanisms for object recognition memory across the lifespan (2015) (10)
Using the Elevated Plus Maze as a Bioassay to Assess the Effects of Naturally Occurring and Exogenously Administered Compounds to Influence Anxiety-Related Behaviors of Mice (2009) (10)
Olanzapine and progesterone have dose-dependent and additive effects to enhance lordosis and progestin concentrations of rats (2002) (10)
Anti-anxiety, cognitive, and steroid biosynthetic effects of an isoflavone-based dietary supplement are gonad and sex-dependent in rats (2011) (10)
In the Ventral Tegmental Area, Progestins’ Membrane-Mediated Actions for Lordosis of Hamsters and Rats Involve Protein Kinase A (2007) (10)
Rats bred for high versus low anxiety responses neonatally demonstrate increases in lordosis, pacing behavior, and midbrain 3α,5α-THP levels as adults (2006) (9)
3α,5α-THP in the raphe magnus attenuates PTZ-induced myoclonic seizures (2001) (9)
Role of pregnane xenobiotic receptor in the midbrain ventral tegmental area for estradiol- and 3α,5α-THP-facilitated lordosis of female rats (2014) (9)
Region-, age-, and sex-specific effects of fetal diazepam exposure on the postnatal development of neurosteroids (2006) (9)
Infusion of 3alpha,5alpha-THP to the pontine reticular formation attenuates PTZ-induced seizures. (2000) (9)
In the ventral tegmental area, progestogens' membrane-mediated actions for lordosis of rats involve the second-messenger phospholipase C (2008) (8)
Infusions of 3alpha,5alpha-THP to the VTA enhance exploratory, anti-anxiety, social, and sexual behavior and increase levels of 3alpha,5alpha-THP in midbrain, hippocampus, diencephalon, and cortex of female rats. (2008) (8)
HORMONES AND GENDER | Female Sex Steroids and Neuronal Excitability (2009) (8)
Estradiol enhances sociosexual behavior and can have proliferative effects in ovariectomized rats (2009) (8)
6-Hydroxydopamine lesions enhance progesterone-facilitated lordosis of rats and hamsters, independent of effects on motor behavior (2010) (8)
Dissociating behavioral, autonomic, and neuroendocrine effects of androgen steroids in animal models. (2012) (8)
Northeast Under/graduate Organization for Neuroscience, A Regional Neuroscience Meeting for Undergraduates, Graduate Students, and Faculty (2004) (8)
Glossolalia is associated with differences in biomarkers of stress and arousal among Apostolic Pentecostals (2011) (7)
3 alpha-OH-DHP and 5 alpha-THDOC implants to the ventral tegmental area facilitate sexual receptivity in hamsters after progesterone priming to the ventral medial hypothalamus. (1993) (7)
Religious-Commitment Signaling and Impression Management amongst Pentecostals: Relationships to Salivary Cortisol and Alpha-Amylase (2015) (6)
The Role and Mechanisms of Steroid Hormones in Approach–Avoidance Behavior (2008) (6)
Oxytocin and/or steroid hormone binding globulin infused into the ventral tegmental area modulates progestogen-mediated lordosis (2010) (6)
Attenuating 5alpha-pregnane-3alpha-ol-20-one formation in the hippocampus of female rats increases pentylenetetrazole-induced seizures. (2005) (6)
Effects of manipulating progesterone and NMDA receptors in the ventral tegmental area for lordosis of hamsters and rats (2008) (6)
Effects of chronic benzodiazepine exposure on stress-induced neuroactive steroid levels (1999) (6)
Progestogens influence cognitive processes in aging. (2009) (5)
Alcohol Dose-Dependently Enhances 3-Androstanediol Formation in Frontal Cortex of Male Rats Concomitant with Aggression (2009) (5)
Effects of non-contingent cocaine on 3alpha-androstanediol. I. Disruption of male sexual behavior (2017) (5)
Analgesic effects of the neurosteroid 3 alpha-androstanediol. (1996) (5)
3alpha,5alpha-THP mediates progestins' effects to protect against adrenalectomy-induced cell death in the dentate gyrus of female and male rats. (2004) (5)
5 alpha-reduced progesterone metabolites are essential in hamster VTA for sexual receptivity. (1994) (5)
Effects of non-contingent cocaine on 3 alpha-androstanediol. II. Disruption of lordosis of proestrous rats (2017) (5)
Progesterone and 3alpha,5alpha-THP enhance sexual receptivity in mice. (2001) (5)
Progestins Have Actions Through GABAA Receptors (2003) (5)
Trilostane exerts antidepressive effects among wild-type, but not estrogen receptor &bgr; knockout mice (2009) (4)
Progesterone's Effects on Cognitive Performance of Male Mice Are Independent of Progestin Receptors but Relate to Increases in GABAA Activity in the Hippocampus and Cortex (2021) (4)
Chronic administration of androgens with actions at estrogen receptor beta have anti-anxiety and cognitive-enhancing effects in male rats (2009) (4)
3_,5_-THP’s Actions in the Ventral Tegmental Area for Lordosis: A Model System for Defining Mechanisms and Function of Progestins (2003) (3)
Northeast Under/graduate Research Organization for Neuroscience (NEURON): our 13th conference for neuroscience trainees and educators. (2009) (3)
Progesterone's 5 alpha-reduced metabolite, 3 alpha,5 alpha-THP, mediates lateral displacement of hamsters. (2005) (3)
3alpha,5alpha-THP in the raphe magnus attenuates PTZ-induced myoclonic seizures. (2001) (3)
Northeast Under/graduate Research Organization for Neuroscience (NEURON): Our Thirteenth Conference for Neuroscience Trainees and Educators (2009) (3)
NorthEast Under/graduate Research Organization for Neuroscience (NEURON): Our Third New York City Meeting (2007) (3)
Rats bred for high versus low anxiety responses neonatally demonstrate increases in lordosis, pacing behavior, and midbrain 3 alpha, 5 alpha-THP levels as adults. (2006) (3)
Central Actions of 3α,5α-THP Involving NMDA and GABAA Receptors Regulate Affective and Sexual Behavior of Female Rats (2020) (3)
The Role of Midbrain 3α,5α-THP in Mediating Exploration, Anxiety, Social, and Reproductive Behavior (2008) (3)
In the ventral tegmental area, G-proteins and cAMP mediate the neurosteroid 3alpha,5alpha-THP's actions at dopamine type 1 receptors for lordosis of rats. (2004) (3)
Antiseizure effects of 5α-androstane-3α,7β-diol may be independent of actions at estrogen receptor β (2008) (2)
3Vα,5α-THP’s Actions in the entral Tegmental Area for Lordosis: A Model System for Defining Mechanisms and Function of Progestins (2003) (2)
Effects of olanzapine infusions to the ventral tegmental area on lordosis and midbrain 3alpha,5alpha-THP concentrations in rats. (2003) (2)
The Vogel Punished Drinking Task as a Bioassay of Anxiety-Like Behavior of Mice (2011) (2)
Prenatal resident-intruder stress decreases levels of allopregnanolone in the cortex, hypothalamus, and midbrain of males, and increases levels in the hippocampus and cerebellum of female, juvenile rat offspring (2020) (2)
Object Recognition - The Role of Hormones Throughout the Lifespan (2011) (2)
Mating Enhances Expression of Hormonal and Trophic Factors in the Midbrain of Female Rats (2020) (2)
Organizational and activational effects of progesterone on social behavior in female mammals (2018) (1)
The 50th anniversary of the discovery of the estrogen receptor — Conversations about hormones then and now (2010) (1)
Infusion of 3 a , 5 a-THP to the pontine reticular formation attenuates 1 PTZ-induced seizures (2000) (1)
Learning and the Lifespan: What’s Sex Got to Do With It? (2020) (1)
Pregnant women with more seizures have lower allopregnanolone concentrations (2021) (1)
Subject Index Vol. 83, 2006 (2006) (0)
Estradiol’s effects on anxiety and depressive behavior of female rats may be due to actions of estrogen receptor beta in the hippocampus (2006) (0)
Advances in Knowledge of Androgens: How Intentional and Accidental Neurosteroid Changes Inform Us of Their Action and Role (2020) (0)
Social stress during pregnancy programs the central neurosteroid system of the offspring (2012) (0)
One Health and the Positive Effects of Alaskan Blueberries (2021) (0)
Androgen-Mediated Effects On Ictal Behavior Among Male Rats Is Mediated Through Pregnane Xenobiotic Receptors, Which Mediated Neurosteroidognesis (P1.265) (2014) (0)
Androgens’ Effects across the Lifespan in Men and Animal Models (2021) (0)
Neurosteroids for a successful pregnancy stress. (2011) (0)
Contents Vol. 83, 2006 (2006) (0)
Social stress during pregnancy programs the central neurosteroid system and hypothalamo-pituitary-adrenal (HPA) axis stress responses of the offspring (2012) (0)
Androgens, autism and more (2010) (0)
Post-Training Administration of Estrogen and/or Androgens with Actions at ERα and/or ERβ to Male Rats Can Improve Performance in the Object Recognition Task (2009) (0)
Stress, inhibition of 5α-reductase, and gestation outcome in rats (2006) (0)
SEX-DEPENDENT OVERWRITING OF PRENATALLY PROGRAMMED STRESS RESPONSES IN RATS WITH NEUROACTIVE STEROIDS (2013) (0)
Subject Index Vol. 84, 2006 (2007) (0)
Book Review:Neurosteroids: A New Regulatory Function in the Nervous System Etienne-Emile Baulieu, Paul Robel, Michael Schumacher (2000) (0)
It's all about the chase: neurosteroidogenesis in male rats is driven by control of mating pace. (2022) (0)
Contents Vol. 84, 2006 (2007) (0)
The Role of 3α-Hydroxy-5α-Pregnan-20-One in Mediating the Development and/or Expression of Schizophrenia Spectrum Disorders: Findings in Rodents Models and Clinical Populations (2011) (0)
Changes in Seizure Frequency Vary Inversely with Changes in Allopregnanolone Levels in Progesterone-Treated Women with Catamenial Epilepsy (S48.006) (2013) (0)
Integration of Affiliation: Well Done! The Integrative Neurobiology of Affiliation, edited by C. Sue Carter, Izja Lederhendler and Brian Kirkpatrick (2000) (0)
Chapter 22 The Role of Midbrain 3a,5a-THP in Mediating Exploration, Anxiety, Social, and Reproductive Behavior (2008) (0)
Acute diet and day of estrous cycle influence nociception in female rats (1992) (0)

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