by Joe
2. August 2009 16:47
An
effect on the subjective sexual response in premenopausal women with
sexual arousal disorder by bremelanotide (PT-141), a melanocortin
receptor agonist
by
Diamond LE, Earle DC, Heiman JR,
Rosen RC, Perelman MA, Harning R.
Palatin Technologies, Inc.,
Cranbury, NJ 08512, USA.
J Sex Med. 2006 Jul;3(4):628-38.
ABSTRACT
T
INTRODUCTION: Melanocortins affect multiple physiological responses,
including sexual behaviors. Bremelanotide is a synthetic peptide
melanocortin analog of alpha-melanocyte-stimulating hormone that is an
agonist at melanocortin receptors MC3R and MC4R. AIM: To evaluate a
single intranasal dose of bremelanotide for potential effects on
physiological and subjective measurements of sexual arousal and desire
in premenopausal women with sexual arousal disorder. MAIN OUTCOME
MEASURES: Change in vaginal pulse amplitude during neutral and erotic
videos after treatment with bremelanotide or placebo and subjects'
perceptions of physiological and sexual response within 24 hours of
treatment with bremelanotide or placebo. METHODS: Eighteen
premenopausal women with a primary diagnosis of female sexual arousal
disorder were randomly assigned to receive a single intranasal dose of
20 mg bremelanotide or matching placebo in a double-blind manner during
the first in-clinic treatment session, and the alternate medication
during the second in-clinic treatment session. During each session,
subjects viewed a 20-minute neutral video followed by a 20-minute
sexually explicit video. Vaginal photoplethysmography was used to
monitor vaginal vasocongestion and questionnaires were used to evaluate
perceptions of sexual response within the following 24-hour period.
RESULTS: More women reported moderate or high sexual desire following
bremelanotide treatment vs. placebo (P = 0.0114), and a trend toward
more positive responses regarding feelings of genital arousal occurred
after bremelanotide compared with placebo (P = 0.0833). Among women who
attempted sexual intercourse within 24 hours after treatment,
significantly more were satisfied with their level of sexual arousal
following bremelanotide, compared with placebo (P = 0.0256). Vaginal
vasocongestion did not change significantly while viewing erotic videos
following bremelanotide administration compared with placebo.
CONCLUSION: This preliminary evaluation suggests the potential for
bremelanotide to positively affect desire and arousal in women with
female sexual arousal disorder and indicates that bremelanotide is a
promising candidate for further evaluation in an at-home study.
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