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首页> 外文期刊>Hormones and behavior >RU486 facilitates or disrupts the sensitization of sexual behaviors by estradiol in the ovariectomized Long-Evans rat: Effect of timecourse
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RU486 facilitates or disrupts the sensitization of sexual behaviors by estradiol in the ovariectomized Long-Evans rat: Effect of timecourse

机译:RU486促进或破坏卵巢切除的Long-Evans大鼠中雌二醇对性行为的敏感性:时程的影响

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摘要

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 5 jig or 10 mu g EB (but not 2 mu g EB), administered every 4 days 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 10 jig), and 5 mg RU486 dissolved in 0.4 mL vehide (VEH; 80% sesame oil, 15% benzyl benzoate, 5% benzyl alcohol) 48 h and 5 h 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 10 pg EB + VEH. As expected, sensitization did not occur in females treated with 2 pg 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. (C) 2015 Elsevier Inc All tights reserved.
机译:向卵巢切除的(OVX)大鼠急性注射雌二醇苯甲酸酯(EB)会激活低水平的脊柱前凸,随后的孕酮(P)给药会加剧脊柱前凸,并招募包括性行为在内的完整性行为模式(例如啤酒花/飞镖和诱骗行为) )。但是,每隔4天对有性经历的OVX大鼠重复注射5夹具或10微克EB(而不是2微克EB)会导致行为过敏,从而使脊柱前凸商(LQs)和食欲行为逐渐增加。我们已经表明,肾上腺P并不起关键作用,因为肾上腺切除术并不能阻止对EB的行为敏感性。在这里,我们通过检查P受体拮抗剂RU486的长期给药效果,以可靠地抑制完全引发的OVX大鼠的性行为,来测试P受体是否发挥作用。在7次测试之前的48小时和5小时,分别用EB(5或10夹具)和5 mg RU486溶解于0.4 mL vehide(VEH; 80%芝麻油,15%苯甲酸苄酯,5%苄醇)中处理雌性动物。分别发生在单层4孔起搏室中,间隔4天。对照动物用2、5,或10 pg EB + VEH治疗。不出所料,用2 pg EB + VEH治疗的女性没有发生致敏作用,并且这些女性的入吸和射精次数少于所有其他组。 RU486并未在早期测试中阻止LQ,中度和高度脊柱前凸幅度(LM2和LM3)的敏感性或食欲性行为,实际上并未增强LQ LM2和LM3的食欲行为,与其在接受EB-治疗的女性中的促进作用一致正如我们和其他人先前所报道的那样。然而,尽管最初有促进作用,但通过长期服用RU486来阻断P受体仍抑制了对EB的行为敏感性维持。 (C)2015 Elsevier Inc.版权所有。

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