2009
DOI: 10.1016/j.physbeh.2008.10.013
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Zaprinast, a phosphodiesterase type-5 inhibitor, alters paced mating behavior in female rats

Abstract: Nitric oxide (NO) is the primary mediator of blood flow in female genital tissues and drugs that enhance the activity of nitric oxide, such as phosphodiesterase type-5 (PDE-5) inhibitors, increase vaginal blood flow in anesthetized rats. The goal of the present study was to test the effects of one PDE-5 inhibitor, zaprinast, on the display of sexual behaviors in gonadectomized, estrogen and progesterone-treated female rats. Experiment 1 demonstrates that zaprinast alters paced mating behavior by lengthening th… Show more

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Cited by 13 publications
(5 citation statements)
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“…Paced mating has been used to evaluate drugs with potential effects on sexual activity in preclinical studies. For example, the phosphodiesterase type-5 (PDE-5) inhibitor, zaprinast, which increases genital blood flow in women, was tested in rats ( Clark et al, 2009 ). They received one of three different doses (1.5, 3, and 6 mg/kg/i.p.)…”
Section: Behavioral Pharmacology Of Paced Matingmentioning
confidence: 99%
“…Paced mating has been used to evaluate drugs with potential effects on sexual activity in preclinical studies. For example, the phosphodiesterase type-5 (PDE-5) inhibitor, zaprinast, which increases genital blood flow in women, was tested in rats ( Clark et al, 2009 ). They received one of three different doses (1.5, 3, and 6 mg/kg/i.p.)…”
Section: Behavioral Pharmacology Of Paced Matingmentioning
confidence: 99%
“…One such possibility is sensitization of sexual arousal via the neural circuit critical for blood flow in the female genitals (Cai, Alexander, & Marson, 2008; Marson & Murphy, 2006). Blood flow appears to be important for the typical display of paced mating behavior (Clark, Guarraci, Megroz, Porter, & Henderson, 2003; Clark, Meerts, & Guarraci, 2009; Gardener & Clark, 2001) so a stronger or faster vasocongestion of the genitals in experienced female rats may contribute to increased tolerance for vaginocervical stimulation (Komisaruk & Whipple, 2000) in sexually experienced rats.…”
Section: Discussionmentioning
confidence: 99%
“…This pattern is characterized by female rats spending less time with a sexual partner, leaving the male more frequently, taking longer to return after receiving sexual stimulation, and displaying fewer solicitation behaviors. We have observed this disruptive pattern when female rats are exposed to drugs that block estrogen receptors or drugs that inhibit PDE-5 (Clark et al, 2003, 2009). Lesions of the medial preoptic area of the hypothalamus also decrease time spent with a sexual partner, increase the likelihood of leaving, and delay returning to the male after receiving sexual stimulation (Yang and Clemens, 2000; Guarraci et al, 2004; Guarraci and Clark, 2006) when subjects are tested for partner preference and during paced-mating behavior.…”
Section: Indications Of Motivationmentioning
confidence: 94%