(Published May 2005)
Anatomic and Physiologic Changes During Female Sexual Response
The female sexual anatomy consists of the outer genitalia or vulva—the labia, interlabial space, clitoris, and vestibular bulb—and the inner genitalia—the vagina, uterus, fallopian tubes, and ovaries.1
Arousal, Orgasm, and Resolution
|TABLE 1. Physiologic and Anatomic Changes Occurring During the Three-Phase Female Sexual Response Model Introduced by Kaplan1-6|
Variety of neurotransmitters (nitric oxide, acetylcholine, vasoactive intestinal peptide) and hormones (oxytocin) that cause vasodilation and increased blood flow to the genitals are releasedVasocongestion occurs in pelvis and breastVagina lubricates
Vagina lengthens and dilates
Uterus rises over levator plate
Other third of vagina tightens and narrows
With clitoral stimulation, clitoris engorges with blood and lengthens and widens
Levator ani, vaginal, and uterine muscles contract
When a woman is sexually aroused, an increase in blood flow to the genitals results in swelling of the labia and vaginal wall (see Table 1).1-6 Lubricating secretions produced by the uterine glands and transudate from the subepithelial vasculature coat the walls of the vagina, and it lengthens and dilates to accommodate the penis, while the uterus rises over the levator plate.1-5 The outer third of the vagina, which is more sensitive to sensation than the inner two-thirds, tightens and narrows, and the introitus is exposed as a result of labial engorgement and opening.3,4
When stimulated, the clitoris, an erectile organ similar to that of the penis, also becomes engorged with blood and increases in length and diameter.1,3 Unlike the penis, the clitoris does not become rigid because it lacks a mechanism for trapping blood within the organ.1,3 Although the clitoris has been described in the past as a “small knob of tissue,” we now know that it is a complex organ that extends deep into the pelvic structure, comprises 18 different (and many hidden) components, and contains 8,000 nerve fibers (twice as many as the penis).1,4 Its sole purpose appears to be to produce sexual pleasure, and the majority of women require stimulation of the clitoris in order to experience orgasm.4 Less than one-third of women regularly have orgasms during sexual intercourse alone.4
Perry and Whipple have identified the Grafenberg or “G” spot as a site that can lead to orgasm when stimulated.7 They describe the G spot as a sensitive area that can be felt through the anterior vaginal wall halfway between the back of the pubic bone and the cervix, along the course of the urethra. Whipple and colleagues conclude that this area may be the female prostate gland.9 The existence of the G spot is controversial, and some researchers contend that it actually represents the roots of the clitoris rather than a separate pleasure zone.5
During orgasm, the levator ani muscles contract approximately eight to 12 times, followed by the vaginal and uterine muscles.3 If stimulation is continued, multiple orgasms may occur. During resolution, the anatomy returns to its normal, unaroused state.2
Along with the anatomical changes that occur during arousal, orgasm, and resolution, a host of physiologic and biochemical events unfold involving the central and peripheral nervous systems. The senses relay sexual images and impulses to the brain, which releases a variety of neurochemicals and neuropeptides, including serotonin, dopamine, epinephrine, norepinephrine, histamine, opioids, gamma-aminobutyric acid, oxytocin, nitric oxide, and vasoactive intestinal peptide.1,2
The brain is so central to female sexual response that imagery alone may be enough to produce orgasm. One study suggests that women may experience a state that appears to be an orgasm via fantasy, without self-stimulation of the genitals.9 In this study, physiologic measurements did not differ between orgasms experienced through fantasy versus masturbation.
The sex hormones estrogen and testosterone also play critical roles in maintaining the health and vitality of the sexual organs and in promoting the libido.2
- Berman JR, Bassuk J. Physiology and pathophysiology of female sexual function and dysfunction. World J Urol 2002;20:111-118.
- Burnett AL, Truss MC. Mediators of the female sexual response: pharmacotherapeutic implications. World J Urol 2002;20:101-105.
- Walton B, Thorton T. Female sexual dysfunction. Curr Wom Health Rep 2003;3:319-326.
- Basson R. Human sex-response cycles. J Sex Marital Ther 2001;27(1):33-43.
- Kerner I. She Comes First: The Thinking Man’s Guide to Pleasuring a Woman. New York, NY: Regan Books; 2004.
- Traish AM, Kim NN, Munarriz R, et al. Biochemical and physiological mechanisms of female genital sexual arousal. Arch Sex Behav 2002;31:393-400.
- Perry JD, Whipple B. Pelvic muscle strength of female ejaculators: evidence in support of a new theory of orgasm. J Sex Res 1981;17:22-39.
- Ladas A, Whipple B, Perry JD. The G Spot and Other Discoveries about Human Sexuality. New York, NY: Holt; 2005.
- Whipple B, Ogden G, Komisaruk BR. Relative analgesic effect of imagery compared to genital self-stimulation. Arch Sex Behav 1992;21:121-133.