Keyword search (4,164 papers available)

"Jones SL" Authored Publications:

Title Authors PubMed ID
1 Disaster-related prenatal maternal stress predicts HPA reactivity and psychopathology in adolescent offspring: Project Ice Storm. Yong Ping E, Laplante DP, Elgbeili G, Jones SL, Brunet A, King S 32442863
PSYCHOLOGY
2 Aromatization Is Not Required for the Facilitation of Appetitive Sexual Behaviors in Ovariectomized Rats Treated With Estradiol and Testosterone. Jones SL, Rosenbaum S, Gardner Gregory J, Pfaus JG 31447629
CSBN
3 Age-specific associations between oestradiol, cortico-amygdalar structural covariance, and verbal and spatial skills. Nguyen TV, Jones SL, Gower T, Lew J, Albaugh MD, Botteron KN, Hudziak JJ, Fonov VS, Louis Collins D, Campbell BC, Booij L, Herba CM, Monnier P, Ducharme S, Waber D, McCracken JT 30776161
PSYCHOLOGY
4 Sensitization of sexual behaviors in ovariectomized Long-Evans rats is induced by a subthreshold dose of estradiol benzoate and attenuated by repeated copulation. Jones SL, Pfaus JG 25251978
PSYCHOLOGY
5 The inhibitory effects of corncob bedding on sexual behavior in the ovariectomized Long-Evans rat treated with estradiol benzoate are overcome by male cues. Jones SL, Antonie RA, Pfaus JG 25960082
PSYCHOLOGY
6 Repeated administration of estradiol promotes mechanisms of sexual excitation and inhibition: Glutamate signaling in the ventromedial hypothalamus attenuates excitation. Jones SL, Farisello L, Mayer-Heft N, Pfaus JG 26008158
PSYCHOLOGY
7 Behavioral defeminization by prenatal androgen treatment in rats can be overcome by sexual experience in adulthood. Jones SL, Cordeaux E, Germé K, Pfaus JG 26163151
PSYCHOLOGY
8 RU486 facilitates or disrupts the sensitization of sexual behaviors by estradiol in the ovariectomized Long-Evans rat: Effect of timecourse. Jones SL, Gardner Gregory J, Pfaus JG 26210062
PSYCHOLOGY
9 Vaginocervical stimulation attenuates the sensitization of appetitive sexual behaviors by estradiol benzoate in the ovariectomized rat. Jones SL, Germé K, Graham MD, Roy P, Gardner Gregory J, Rosenbaum S, Parada M, Pfaus JG 26278846
PSYCHOLOGY
10 Facilitation of sexual behavior in ovariectomized rats by estradiol and testosterone: A preclinical model of androgen effects on female sexual desire. Jones SL, Ismail N, Pfaus JG 28278441
PSYCHOLOGY

 

Title:RU486 facilitates or disrupts the sensitization of sexual behaviors by estradiol in the ovariectomized Long-Evans rat: Effect of timecourse.
Authors:Jones SLGardner Gregory JPfaus JG
Link:https://www.ncbi.nlm.nih.gov/pubmed/26210062?dopt=Abstract
Publication:
Keywords:
PMID:26210062 Category:Horm Behav Date Added:2019-05-31
Dept Affiliation: PSYCHOLOGY
1 Center for Studies in Behavioral Neurobiology, Department of Psychology, Concordia University, Montreal, QC H4B 1R6, Canada. Electronic address: sherri.jones@concordia.ca.
2 Center for Studies in Behavioral Neurobiology, Department of Psychology, Concordia University, Montreal, QC H4B 1R6, Canada.

Description:

RU486 facilitates or disrupts the sensitization of sexual behaviors by estradiol in the ovariectomized Long-Evans rat: Effect of timecourse.

Horm Behav. 2015 Sep;75:1-10

Authors: Jones SL, Gardner Gregory J, Pfaus JG

Abstract

An acute injection of estradiol benzoate (EB) to the ovariectomized (OVX) rat activates low levels of lordosis, and subsequent progesterone (P) administration augments lordosis and recruits a complete pattern of sexual behavior including appetitive behaviors (e.g., hops/darts and solicitations). However, repeated injections of 5µg or 10µg EB (but not 2µg EB), administered every 4days to sexually-experienced OVX rats results in a behavioral sensitization, such that lordosis quotients (LQs) and appetitive behaviors progressively increase. We have shown that adrenal P does not play a critical role because behavioral sensitization to EB is not prevented by adrenalectomy. Here we tested whether P receptors play a role by examining the effect of chronic administration of the P receptor antagonist RU486 at a dose that reliably inhibits sexual behavior in fully primed OVX rats. Females were treated with EB (5 or 10µg), and 5mg RU486 dissolved in 0.4mL vehicle (VEH; 80% sesame oil, 15% benzyl benzoate, 5% benzyl alcohol) 48h and 5h prior to each of 7 tests, respectively, occurring at 4-day intervals in unilevel 4-hole pacing chambers. Control animals were treated with 2, 5, or 10µg EB+VEH. As expected, sensitization did not occur in females treated with 2µg EB+VEH, and those females received fewer intromissions and ejaculations than all other groups. RU486 did not prevent the sensitization of LQ, moderate and high lordosis magnitudes (LM2 and LM3) or appetitive sexual behaviors on early tests, and in fact potentiated appetitive behaviors, LQ, LM2 and LM3, consistent with its facilitative actions in females treated with EB-alone, as we and others have reported previously. However, despite the initial facilitation, blocking P receptors by chronic administration of RU486 inhibited the maintenance of behavioral sensitization to EB.

PMID: 26210062 [PubMed - indexed for MEDLINE]





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