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Female ejaculation and squirting as similar but completely different phenomena: A narrative review of current research

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Clinical Anatomy
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Women expel fluids of various quantities and compositions from the urethra during sexual arousal and orgasm. These are classified as either female ejaculation (FE) or squirting (SQ). The aim of our analysis was to present evidence that FE and SQ are similar but etiologically different phenomena. A review of studies was performed on fluids expelled from the urogenital tract during female sexual activities using the Web of Knowledge™ (Web of Science Core Collection) and MEDLINE (Ovid) databases from 1946 to 2021. Until 2011, all female orgasmic expulsions of fluids were referred to as FE. The fluid was known to be either from the paraurethral glands or as a result of coital incontinence. At present, SQ is considered as a transurethral expulsion of approximately 10 milliliters or more of transparent fluid, while FE is considered as a secretion of a few milliliters of thick fluid. The fluid in SQ is similar to urine and is expelled by the urinary bladder. The secretion in FE originates from the paraurethral glands and contains a high concentration of prostate‐specific antigen. Both phenomena can occur simultaneously. The mechanisms underlying SQ and FE are entirely different. SQ is a massive transurethral orgasmic expulsion from the urinary bladder, while FE is the secretion of a very small amount of fluid from the paraurethral glands.
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REVIEW
Female ejaculation and squirting as similar but completely
different phenomena: A narrative review of current research
Zlatko Pastor | Roman Chmel
Obstetrics and Gynecology Department,
University Hospital Motol and 2nd Medical
Faculty of Charles University, Prague,
Czech Republic
Correspondence
Zlatko Pastor, Obstetrics and Gynecology
Department, University Hospital Motol, V
Úvalu 84, Prague 5 150 06, Czech Republic.
Email: pastor.zlatko@volny.cz
Abstract
Women expel fluids of various quantities and compositions from the urethra during sex-
ual arousal and orgasm. These are classified as either female ejaculation (FE) or squirting
(SQ). The aim of our analysis was to present evidence that FE and SQ are similar but eti-
ologically different phenomena. A review of studies was performed on fluids expelled
from the urogenital tract during female sexual activities using the Web of Knowledge
(Web of Science Core Collection) and MEDLINE (Ovid) databases from 1946 to 2021.
Until 2011, all female orgasmic expulsions of fluids were referred to as FE. The fluid
was known to be either from the paraurethral glands or as a result of coital inconti-
nence. At present, SQ is considered as a transurethral expulsion of approximately 10 mil-
liliters or more of transparent fluid, while FE is considered as a secretion of a few
milliliters of thick fluid. The fluid in SQ is similar to urine and is expelled by the urinary
bladder. The secretion in FE originates from the paraurethral glands and contains a high
concentration of prostate-specific antigen. Both phenomena can occur simultaneously.
The mechanisms underlying SQ and FE are entirely different. SQ is a massive transure-
thral orgasmic expulsion from the urinary bladder, while FE is the secretion of a very
small amount of fluid from the paraurethral glands.
KEYWORDS
female ejaculation, female prostate, orgasm, paraurethral glands, sexual arousal, squirting,
urinary bladder
1|INTRODUCTION
Female sexual arousal is manifested in the genital area primarily
through vaginal lubrication, which results from plasma ultrafiltration in
the perivaginal vascular plexuses into the lumen of the vagina
(Levin, 2003; Pastor, 2013). However, during the orgasm, some
women can squirt or expel up to hundreds of milliliters of fluid. Until
2011, due to the similarity to male ejaculation, all fluids expelled dur-
ing ejaculation orgasm (EO) were considered as female ejaculation
(FE) without proper distinction among into FE, squirting (SQ), or coital
incontinence (CI). This ambiguity caused diagnostic confusion and
controversial conclusions (Rubio-Casillas & Jannini, 2011). SQ and FE
are considered physiological but uncommon sexual responses and CI
is a symptom of a disorder, such as urinary incontinence
(Pastor, 2013; Pastor & Chmel, 2018). The fluid outflow during sexual
activities usually manifests as wetness, secretion, or gushes (Pastor &
Chmel, 2018). The uncertainties regarding orgasmic fluid relate partic-
ularly to their origin, volume, composition, and expulsion mechanism.
Previous studies did not have a uniform, objective methodology and
were mostly based on the women's subjective sensations without
adequate diagnostic examination to verify the fluid source, such as
ultrasonography, urinary bladder catheterization, and video visualiza-
tion (Addiego et al., 1981; Belzer Jr, 1981; Belzer Jr, 1982; Bullough
et al., 1984; Darling et al., 1990; Davidson et al., 1989; Heath, 1987;
Ladas et al., 2005; Perry & Whipple, 1981; Whipple &
Komisaruk, 1991; Zaviačič, 1999; Zaviačičet al., 2000; Zaviačič,
Received: 17 February 2022 Revised: 3 April 2022 Accepted: 4 April 2022
DOI: 10.1002/ca.23879
© 2022 American Association for Clinical Anatomists and the British Association for Clinical Anatomists.
Clinical Anatomy. 2022;110. wileyonlinelibrary.com/journal/ca 1
Doležalová, et al., 1988; Zaviačič, Zaviačičová, et al., 1988). The pres-
ence of prostate-specific antigen (PSA) has been considered as con-
clusive evidence that EO fluid originates from the paraurethral glands
(often referred to as the female prostate in sexological literature),
(Bullough et al., 1984; Dietrich et al., 2011; Wimpissinger et al., 2013;
Zaviačič, 1999; Zaviačičet al., 2000; Zaviačič, Doležalová, et al., 1988;
Zaviačič, Zaviačičová, et al., 1988). Although the secretion from
female prostate can contaminate other fluids secreted during sexual
activities (Pastor, 2013; Rubio-Casillas & Jannini, 2011; Salama
et al., 2015). While the classification and differential diagnosis for EO
have been proposed previously, (Levin et al., 2016; Pastor, 2013;
Pastor & Chmel, 2018; Rogers et al., 2018; Rubio-Casillas &
Jannini, 2011; Salama et al., 2015) it is rarely used both in practice
and in studies. The differences among sexual fluids are known at pre-
sent (Pastor, 2013; Pastor & Chmel, 2018; Rodriguez et al., 2021;
Rubio-Casillas & Jannini, 2011; Salama et al., 2015; Schubach, 2001)
However, orgasmic fluid excretion is often universally considered FE,
and the fluid itself is considered an ejaculate from female prostate
because it contains PSA (Rodriguez et al., 2021). This review aimed to
clarify the inaccuracies regarding sexualfluids and highlight the dif-
ferences between FE and SQ.
2|MATERIALS AND METHODS
The systematic literature search of Web of Knowledge(Web of Sci-
ence of Core Collection) and MEDLINE (Ovid) articles published
between 1946 and 2021 was performed. The day of the last search
was December 13, 2021. The keyword female ejaculationwas com-
bined with female prostate,”“squirting,”“paraurethral (Skene's)
glands,and orgasm.The search was limited to English language and
human studies (available only in Ovid). In total, 338 articles were
obtained (Web of Science: n=292; Ovid: n=46).
The duplicates were discarded (n=18). The full-text articles and
abstracts were studied, and the articles exclusively referring to CI and
its therapy or those having inaccurate terminology or speculative con-
tent were excluded (n=294). The list of 294 eligible articles was man-
ually rechecked, and 20 additional suitable studies and books were
added to the final list of literature sources relevant to this study.
Finally, a total of 46 studies were included (Figure 1).
3|RESULTS
The articles on female expulsion of fluid during orgasm contain incon-
sistent results and controversial conclusions. Most studies were based
on these traditional premises:
(a) the expelled fluid is a single identical phenomenon usually
referred to as FE (Addiego et al., 1981; Bullough et al., 1984; Darling
et al., 1990; Ladas et al., 2005; Whipple & Komisaruk, 1991;
Wimpissinger et al., 2007; Wimpissinger et al., 2009; Wimpissinger
et al., 2013; Zaviačič, 1999; Zaviačičet al., 2000; Zaviačič, Doležalová,
et al., 1988; Zaviačič, Zaviačičová, et al., 1988).; (b) the source of the
fluid is the female prostate (paraurethral glands) (Rogers et al., 2018;
Zaviačič, 1999; Zaviačičet al., 2000; Zaviačič, Doležalová, et al., 1988;
Zaviačič, Zaviačičová, et al., 1988); (c) FE is highly prevalent (Bullough
FIGURE 1 Preferred reporting items for
systematic reviews and meta-analyses
(PRISMA) diagram showing methodology of
the systematic literature search
2PASTOR AND CHMEL
et al., 1984; Darling et al., 1990; Heath, 1987; Zaviačič, 1999; Zaviačič
et al., 2000; Zaviačič, Doležalová, et al., 1988; Zaviačič, Zaviačičová,
et al., 1988); (d) a relatively large volume of fluid is expelled (Bullough
et al., 1984; Goldberg et al., 1983; Heath, 1987; Zaviačič, 1999;
Zaviačičet al., 2000; Zaviačič, Doležalová, et al., 1988; Zaviačič,
Zaviačičová, et al., 1988); (e) the sexualfluid has a high-PSA concen-
tration (Rogers et al., 2018; Wimpissinger et al., 2007; Zaviačič, 1999;
Zaviačičet al., 2000; Zaviačič, Doležalová, et al., 1988; Zaviačič,
Zaviačičová, et al., 1988); (f) the expulsion of fluid is provoked by the
stimulation of the clitorourethrovaginal complex (Addiego et al., 1981;
Rubio-Casillas & Jannini, 2011; Zaviačič, 1999; Zaviačičet al., 2000;
Zaviačič, Doležalová, et al., 1988; Zaviačič, Zaviačičová, et al., 1988).
3.1 |Sources, types, and nature of ejaculation
orgasm
The fluids expelled during sexual arousal or orgasm can be divided
into four categories: vaginal lubrication, which is a physiological and
desirable manifestation of arousal; FE and SQ, which are physiological
but sporadic phenomena; and symptoms of orgasmic urinary inconti-
nence (Figure 2) (Pastor, 2013).
FE and SQ vary according to the source, volume, color, fluid con-
sistency, expulsion type, PSA concentration, manifestation, expulsion
mechanism, subjective sensations, and biochemical composition
(Table 1) (Pastor, 2013).
3.2 |Prevalence of fluids expelled during sexual
arousal and orgasm
Studies on EO describe either sporadic incidence or prevalence rang-
ing between 4.6% and 54% (Table 2) (Bullough et al., 1984; Darling
et al., 1990; Masters & Johnson, 1966; Perry & Whipple, 1981). Mas-
ters et al. described EO in only 14 women (4.6%) of their study group
of 300 patients aged 1840 years. In a cohort of a thousand women
undergoing sex therapy programs, only a handfulof women
reported fluid ejaculatedduring orgasm (Masters et al., 1988). The
studies describing the high prevalence of FE in hundreds of cases are
based only on questionnaire studies and women's subjective feelings
(Bullough et al., 1984; Darling et al., 1990; Davidson et al., 1989;
Ladas et al., 2005; Whipple & Komisaruk, 1991; Wimpissinger
et al., 2013). Only three previous studies distinguish between FE and
SQ (Rubio-Casillas & Jannini, 2011; Salama et al., 2015;
Schubach, 2001). Other papers describe EO without an exact distinc-
tion about which phenomenon is involved (Belzer Jr, 1981; Bullough
et al., 1984; Darling et al., 1990; Dwyer, 2012; Goldberg et al., 1983;
Masters & Johnson, 1966; Perry & Whipple, 1981; Wimpissinger
et al., 2007; Wimpissinger et al., 2009; Wimpissinger et al., 2013;
Zaviačič, 1999; Zaviačičet al., 2000; Zaviačič, Doležalová, et al., 1988;
Zaviačič, Zaviačičová, et al., 1988). In an online study, Wimpissinger
et al. studied 320 women with EO aged 1873 years. In total, 19% of
women ejaculated in 91%100% of their coitus, and 14% of
FIGURE 2 Overview of possible fluids expelled during orgasm according to the source
TABLE 1 Comparison of the characteristics of FE and SQ
Female ejaculation Squirting
Source Paraurethral glands Urinary bladder
Volume Approximately up to
1ml
Tens to hundreds of ml
Color Whitish, milky Clear, transparent,
yellowish
Consistence Thick Thin
Expulsion
type
Secretion, discharge Squirt
PSA +++ 0/+
Manifestation Wetness/secretion/
discharge/
asymptomatic
Massive expulsions of
transparent fluid
Expulsion
mechanism
Gland secretion (leakage
of secretion)
Transurethral expulsion
(detrusor muscle
contraction)
Subjective
feeling
Orgasm/sexual arousal/
asymptomatic
Orgasm/high-sexual
arousal
Uric acid,
urea,
creatinine
++
Glucose +++ +
Fructose +++ +
Abbreviations: PSA, prostate specific antigen; +++, large quantity; ++,
moderate quantity; +, small quantity; , not present.
PASTOR AND CHMEL 3
respondents reported EO in 1%10% of their coitus. On average, 57%
of women had experienced EO. Nevertheless, the study did not report
the real prevalence of EO as the group size from which the respon-
dents were recruited was not mentioned (Wimpissinger et al., 2013).
Some studies claim that the fluid produced during EO comes from the
female prostate, (Bullough et al., 1984; Zaviačič, 1999; Perry &
Whipple, 1981; Darling et al., 1990; Wimpissinger et al., 2007. but
other studies describe EO as urine expelled during CI (Bohlen, 1982;
Goldberg et al., 1983; Jha et al., 2012; Korda et al., 2010; Nilsson
et al., 2011; Serati et al., 2011; Vierhout & Gianotten, 1993).
3.3 |Paraurethral glands
The paraurethral glands (female prostate) are considered the source of
fluid in realFE (Pastor, 2013; Rubio-Casillas & Jannini, 2011). Female
prostate is found in every 23 women (Dietrich et al., 2011;
Dwyer, 2012; Wimpissinger et al., 2009). Its weight ranges from 2.6 to
5.2 g, which is approximately five times smaller than the male prostate
(Huffman, 1948; Zaviačičet al., 2000). The female prostate contains
glands, ducts, and musculofibrotic tissue. The ratio of the volume of the
ducts and fibrous structures to the glandular component in female
prostate is different from that of the male prostate since female pros-
tate has a smaller glandular component (Huffman, 1948). Moreover, its
secretion volume reaches a maximum of 24 ml (Wimpissinger
et al., 2009). The separate glands are localized periurethral, with
approximately 20 ducts opening to the lumen of the urethra (Figure 3)
(Huffman, 1948; Zaviačičet al., 2000). Occasionally, the ducts pass
along the urethra with outlets in the vaginal vestibulum (Dwyer, 2012).
Female prostate secretion contains PSA, prostate-specific alkaline
phosphatase, fructose, and glucose (Zaviačič, Doležalová, et al., 1988).
Rubio-Casillas and Jannini demonstrated a decreasing concentration
gradient of PSA in the fluids as follows: FE > urine>SQ > vaginal secre-
tion (Rubio-Casillas & Jannini, 2011). Notably, the function of female
prostate remains unclear. A protective antimicrobial effect of its fluid
has been speculated previously (Moalem & Reidenberg, 2009).
TABLE 2 Prevalence of EO relative to the sample size of the respondents and the corresponding
Prevalence Sample size of respondents Research methodology Authors, year of study
Handful 1000 Sex therapy program interview Masters & Johnson, 1966
4.6% 300 Sex therapy program interview Masters et al., 1988
10%40% 47 Self-reporting questionnaire
Individual interview
Perry & Whipple, 1981
14%54% 227 Conversation after an oral practical presentation Bullough et al., 1984
40% 1289 Self-reporting questionnaire Darling et al., 1990
Abbreviation: EO, ejaculation orgasm.
FIGURE 3 Localization of
paraurethral glands, which open to the
lumen of the distal urethra
4PASTOR AND CHMEL
Zaviačičet al. described five types of female prostate according
to its localization: meatal (66%), posterior (10%), rudimentary (8%),
whole length (6%), and others (10%) (Zaviačičet al., 2000). Meanwhile,
Romashchenko et al. reported only four types of female prostate: dis-
tal (65%), proximal (23%), whole length (7%), and others (5%)
(Figure 4) (Romashchenko et al., 2018).
3.4 |Volume, source, and mechanism of fluid
secretion during EO
The volume of fluid released during EO ranges from a few to hun-
dreds of ml and is usually described as FE (Table 3) (Belzer Jr, 1981;
Belzer Jr, 1982; Bullough et al., 1984; Goldberg et al., 1983;
Heath, 1987; Rubio-Casillas & Jannini, 2011; Salama et al., 2015;
Wimpissinger et al., 2009; Wimpissinger et al., 2013; Zaviačič,
Doležalová, et al., 1988). Some authors speculate that FE fluid is simi-
lar to urine in CI (Goldberg et al., 1983).
The fluid in FE is considered to be produced by the female pros-
tate (Addiego et al., 1981; Belzer Jr, 1982; Cabello Santamaria, 1991;
Wimpissinger et al., 2007; Zaviačič, Doležalová, et al., 1988; Zaviačič,
Zaviačičová, et al., 1988) or the urinary bladder, in which the fluid can
be contaminated with PSA from female prostate, similar to urine
(Rubio-Casillas & Jannini, 2011; Salama et al., 2015; Schubach, 2001)
Schubach first demonstrated the mechanism underlying SQ as the
expulsion of fluid from the urinary bladder using an inserted Foley
catheter. Additionally, milky-white, mucous-like excretion from the
urethra outside the catheterwas observed in four women and was
considered female prostate secretion (Schubach, 2001). Rubio-Casillas
and Janinni collected 120 ml of fluid coming from the urethra during
SQ. Meanwhile, 1 ml of FE, described as very scanty, thick, and whit-
ish fluid,was collected using a sterile tong depressor from the outer
urethral orifice (Rubio-Casillas & Jannini, 2011). Using ultrasound
examination, Salama et al. confirmed the origin of SQ to be the urinary
bladder. In seven women, filling of the urinary bladder using
ultrasound was examined: (a) after voluntary micturition, (b) during
sexual stimulation immediately before SQ, and (c) immediately after
SQ. Involuntary expulsion of urine during orgasm was confirmed
(Salama et al., 2015).
The normal maximum capacity of the urinary bladder reaches up
to 400500 ml. The urinary bladder is a reservoir of fluid expulsed
transurethrally during SQ, expulsed by the strong contraction of the
detrusor muscle (Pastor, 2013; Rubio-Casillas & Jannini, 2011; Salama
et al., 2015; Schubach, 2001). Due to the limited glandular capacity of
the female prostate, as demonstrated by magnetic resonance imaging,
female prostate cannot produce a volume of more than a few ml of
FIGURE 4 Most common localizations of the paraurethral glands and ducts: (A) distal (meatal) urethra, (B) proximal urethra, and (C) along the
whole urethra
TABLE 3 Volume of fluid excreted during sexual arousal and
orgasm in studies of FE, studies of SQ, and studies without distinction
between these phenomena
Author and year of study
publication Volume of fluid described only as FE
Addiego et al., 1981 1 to few ml
Zaviačič, 1988 15ml
Belzer Jr, 1982 10 ml
Bullough et al., 1984 312 ml
Goldberg et al., 1983 315 ml
Heath, 1987 3050 ml
Wimpissinger et al., 2013 0.3150 ml and more
Author and year of study
publication
Volume of fluid with distinction
between FE and SQ
Schubach, 2001 2 ml (FE) 50500 ml (SQ)
Rubio-Casillas &
Jannini, 2011
1 ml (FE) 120 ml (SQ)
Salama et al., 2015 15110 ml
(median 60 ml) (SQ)
Pastor & Chmel, 2018 60 ml (SQ)
Abbreviations: FE, female ejaculation; SQ, squirting.
PASTOR AND CHMEL 5
thick secretion (Figure 5) (Lawrentschuk & Perera, 2000; Pastor &
Chmel, 2018; Wimpissinger et al., 2009). The glandular structures of
the female prostate are distributed along the urethral wall, while in
the male prostate, glandular structures are localized around the proxi-
mal urethra (Figure 6). Aside from the myofibrils, the female prostate
does not have effective smooth muscle contractile fibers for massive
fluid expulsion (Zaviačičet al., 2000).
3.5 |Biochemical parameters of the fluid expulsed
during SQ and FE
The volume of the fluid produced by the female prostate is small,
approximately less than 1 ml. The fluid is thick in consistency, whitish
in color, and contains PSA, glucose, and fructose. On the other hand, a
large volume of clear fluid, up to hundreds of ml, is ejected trans-
urethrally by the detrusor muscle contraction in SQ (Rubio-Casillas &
Jannini, 2011; Salama et al., 2015; Schubach, 2001). Urea, creatinine,
and uric acid in the SQ fluid confirm that it comes from the kidneys
and is collected in the urinary bladder. There is no agreement on
whether the biochemical composition of SQ fluid is identical to urine
or is actually its diluted form (Pastor & Chmel, 2018; Rodriguez
et al., 2021; Rubio-Casillas & Jannini, 2011; Salama et al., 2015;
Schubach, 2001). Two studies reported that SQ fluid is the diluted
urine, (Rubio-Casillas & Jannini, 2011; Schubach, 2001) while others
assumed that it is biochemically identical with urine (Table 4)
(Goldberg et al., 1983; Pastor & Chmel, 2018; Salama et al., 2015).
Goldberg et al. describe SQ as the expulsion of colorless, odorless,
and tasteless fluid (Goldberg et al., 1983).
There is a consensus on FE regarding its source (paraurethral
glands), volume (up to 1 ml), appearance (thick consistency and whit-
ish color), mechanism of expulsion (secretion), and composition (high
levels of PSA, glucose, and fructose) (Rubio-Casillas & Jannini, 2011;
Salama et al., 2015; Schubach, 2001).
4|DISCUSSION
The massive orgasmic transurethral expulsion during sexual activity is
called SQ, and the SQ fluid originates from the urinary bladder. The
term FE should be reserved for the expulsion of a small volume of
thick secretion from the female prostate, which can also be asymp-
tomatic. Both phenomena have different etiologies, mechanisms, and
manifestations (Pastor, 2013; Pastor & Chmel, 2018; Rubio-Casillas &
Jannini, 2011; Salama et al., 2015; Schubach, 2001). Their inter-
changing causes much confusion and derails from the correct identifi-
cation of the two different phenomena, as we observe in research. In
this review, we reported the high prevalence of EO (up to 54%)
referred to as FE (Bullough et al., 1984; Darling et al., 1990;
Heath, 1987; Wimpissinger et al., 2013) by merging similar but
FIGURE 5 The contrast between
large-capacity fluid collection in the
urinary bladder, expulsed by contraction
of the detrusor muscle during SQ (yellow),
and the small volume of fluid excretion
from paraurethral glands, due to the
contraction of the fine periurethral
myofibrils (red) during FE. FE, female
ejaculation; SQ, squirting
FIGURE 6 The localization, volume,
and ratio of glands, ducts, and fibro-
muscular connective tissue of the
paraurethral glands compared to those in
the male prostate
6PASTOR AND CHMEL
etiologically distinct phenomena (SQ, FE, vaginal lubrication, and CI)
that are incorrectly labeled with one umbrella term (FE). We consider
SQ a sporadic manifestation of sexual arousal and orgasm that can
occur in highly aroused and multi-orgasmic women. A realistic estima-
tion of the prevalence of SQ could be approximately 5% (Masters
et al., 1988; Masters & Johnson, 1966).
4.1 |Presence of PSA in expelled fluids
The presence of PSA in the fluid excreted during sexual activity is not
conclusive evidence of the exclusive origin of the female prostate
fluid. The admixture of PSA is also found in other fluids (Rubio-
Casillas & Jannini, 2011). Female prostate secretion into the urethra
may contaminate urine, vaginal lubrication, or SQ fluid.
4.2 |Terminological inaccuracies about the female
ejaculate
To date, the term female ejaculate is mainly used to describe all fluids
emitted during orgasm. More accurately, this fluid is mainly from FE
or SQ. The difference between these two terms, in terms of their simi-
larity to urine, has been discussed (Rodriguez et al., 2021). In our opin-
ion, the ambiguity between these two terms may unnecessarily
complicate previous and future clinical and anatomical research. It has
been well established that the fluid in FE is expelled from the female
prostate, and the fluid in SQ is expelled from the urinary bladder. In
CI, the leakage of urine is related to stress urinary incontinence or an
overactive urinary bladder (Pastor & Chmel, 2018; Rubio-Casillas &
Jannini, 2011; Salama et al., 2015; Schubach, 2001).
4.3 |Origin, volume, and mechanism of fluid
expulsion during female sexual arousal and orgasm
There are three potential sources of female sexual fluids: the urinary
bladder, the vagina, and the paraurethral glands. Notably, it could also
be a combination of these (Pastor, 2013). The urinary bladder is the
only organ that can collect up to hundreds of ml of fluid, which is
expulsed through the urethra as a squirt using the strong contractions
of the detrusor muscle. Female prostate is not present in all women
(Dietrich et al., 2011; Dwyer, 2012; Wimpissinger et al., 2009); more-
over, it cannot be the source of massive SQ. The female prostate has a
small secretion capacity and does not have the adequate muscle for a
strong contraction. Fine myofibrils surround the separated female pros-
tate glands with minimal contractile activity. Simultaneous SQ of a large
volume of fluid is not possible from approximately 20 ducts in the para-
urethral glands. Female prostate is localized around the external meatus
of the urethra. This minimizes the kinetic energy required to expulse a
small volume of fluid from the dilated urethral orifice overlapped by the
labia minora. The delicate fibers of the sphincter muscle around the
proximal urethra contract during sexual arousal and orgasm, and, there-
fore, urine should not be expelled during orgasm (Korda et al., 2010;
Lawrentschuk & Perera, 2000). However, this paradigm is true for men
but unequivocally not for women (Rubio-Casillas & Jannini, 2011). In
women, orgasm may trigger involuntary urinary bladder contractions,
which suppress the urethral and urinary bladder sphincter and may lead
to the leakage of urine from the urinary bladder (Khan et al., 1988).
Thus, pulse contractions of the detrusor muscle may cause spraying.
Sensory adjustment of receptors in the urinary bladder varies per indi-
vidual. In some women, urinary bladder filling during orgasm may
prompt emptying. In contrast to patients with CI, SQ provides women
with maximal sexual catharsis. Notably, unwanted leakage of actual
urine can be psychotraumatic for some women (Pastor, 2013;
Wimpissinger et al., 2013). Women with SQ do not suffer from overac-
tive urinary bladder (Cartwright et al., 2007; Pastor, 2013) or stress uri-
nary incontinence due to increased urethrovaginal junctional mobility
(Pastor, 2013; Perry & Whipple, 1981).
4.4 |Biochemical composition and densities of
fluids expelled during FE and SQ
Most women do not consider fluid during SQ to be urine and believe
that the expulsed fluid is different in smell, taste, and appearance
TABLE 4 The results from the biochemical analysis of the fluid expelled during SQ
Author
Sample
size Volume (ml) Urea (mmol/L)
Creatinine
(mmol/L)
Uric acid
(mmol/L) PSA (ng/ml) Density
Glucose
fructose
SQ producing fluid with a composition identical to urine
Salama
et al., 2015
715110
(median: 60)
307 (62376) 9.3 (1.917.9) 2.6 (0.13.5) 0.72 (03.74) N/A N/A
Pastor &
Chmel, 2018
1 60 299 7.9 3,0 0.55 1005 Negative
SQ producing fluid with a composition identical to diluted urine
Schubach, 2001 7 50500 87398 946 N/A N/A N/A Negative
Rubio-Casillas &
Jannini, 2011
1 120.67 ± 56.36 417.0 ± 42.88 21.37 ± 4.16 10.37 ± 1.48 0.23 ± 0.25 1001.67 ± 2.89 N/A
Abbreviations: N/A, not available; PSA, prostate specific antigen; SQ, squirting.
PASTOR AND CHMEL 7
(Goldberg et al., 1983). The excreted fluid can be biochemically identi-
cal to urine but can also be considered diluted urine with different
osmolarities and concentrations of urea, creatinine, and uric acid.
Because the biochemical composition of urine can change in different
situations (e.g., dehydration or increased glomerular filtration in the
kidneys), it can be diluted, clear, and odorless during increased sexual
arousal. The concentration of urinary metabolites depends on the
actual volume and osmolarity of urine at the onset of sexual stimula-
tion until the moment of SQ. When a large volume of concentrated
urine is in the urinary bladder just before sex, the expelled fluid may
be identical to urine. Conversely, initiation of stimulation shortly after
voiding may produce diluted urine with low osmolality. The urinary
bladder could be filled relatively quickly by the residual urine from the
ureters and renal pelvis and by frequent pulses of ureters. The
changes in the osmolality of urine could be caused by the psycho-
sexual condition of increased blood pressure and glomerular filtration
rate and the secretion of the antidiuretic hormone vasopressin.
Together with corticoliberin, these changes mobilize defense mecha-
nisms against emotional stressors. During sexual relaxation and emo-
tional intimacy, vasopressin serum concentration and urine osmolality
decrease (Carter, 2017). The effect of aldosterone on reabsorptive
mechanisms in the kidneys could also be considered a contributory
factor (Schubach, 2001). These pathophysiological consequences and
precoital habits (e.g., micturition) could be some causes of the differ-
ences in urine concentration during SQ in different situations.
4.5 |Initiation of SQ and FE according to the
anatomic location of sexual stimulation
SQ is achieved mainly through the stimulation of the
clitorourethrovaginal complex (Rubio-Casillas & Jannini, 2011)
through the glans clitoridis and through vaginal stimulation of the dor-
sal part of the clitoris (corpus clitoridis and bulbus vestibuli) during
masturbation or coitus. FE is induced by a similar mechanism but
occurs most frequently during transvaginal stimulation of the distal
part of the anterior vaginal wall during urethral stimulation (Zaviačič,
Zaviačičová, et al., 1988). However, FE seems to be a direct mechani-
cal extrusion of fluid from the female prostate. FE and SQ could also
be induced during stimulation of other extragenital erogenous zones.
4.6 |Opinions on FE and SQ and their impact on
the general population
The diverse conclusions of studies to date reflect how sexual aspects
have been incompletely explored. This ambiguity can inadequately
affect the opinions of experts and the general population on different
sexual standards.Inaccurate or incomplete information about FE
and SQ as a frequent symptom of sexual arousal (e.g., one in two
women) (Wimpissinger et al., 2013) can cause frustration and mislead
women experiencing these symptoms. Moreover, many erotic videos
with abundant squirts of sexual fluid are showing this sexual
phenomenon as a natural part of orgasm. Unfortunately, it can result
in a feeling of sexual imperfection in women without SQ and may set
unrealistic expectations for men. On the other hand, although not
considered scientifically relevant, erotic videos and other similar mate-
rials demonstrate transurethral SQ of a large volume of watery fluid
with an extraordinary pressure gradient and thus, at least, dispel
doubts about its origin.
4.7 |Limitations and weaknesses of the review
This review has some limitations. First, it includes studies with con-
flicting terminology, inconsistent methodology, and limited use of imag-
ing methods to objectively confirm their conclusions (Addiego
et al., 1981; Bullough et al., 1984; Zaviačič, 1999; Zaviačičet al., 2000;
Zaviačič,Doležalová, et al., 1988; Zaviačič,Zaviačičová, et al., 1988);
(Belzer Jr, 1981; Belzer Jr, 1982; Darling et al., 1990; Davidson
et al., 1989; Heath, 1987; Ladas et al., 2005; Whipple &
Komisaruk, 1991). The heterogeneity of the analyzed studies caused dif-
ficulties in their comparison. Second, all selected studies were assessed
to maximize objectivity. However, some of them were inaccurate and
had generally accepted conclusions (Ladas et al., 2005). Third, it was dif-
ficult to justify some opinions on FE and SQ when only a limited number
of studies were available to support the conclusions of this review
(Pastor, 2013; Pastor & Chmel, 2018; Rubio-Casillas & Jannini, 2011;
Salama et al., 2015; Schubach, 2001). Nevertheless, this review refuted
some traditional misconceptions concerning FE and SQ, which were not
confirmed by adequate research methods, by studying relevant scientific
studies and generally accepted anatomical and physiological facts.
5|CONCLUSION
Relevant and robust studies confirmed that FE and SQ are entirely dif-
ferent physiological sexual phenomena with low prevalence in
women. FE and SQ are not a common part of female sexual arousal
and orgasm. Incorrect assessment of the manifestation of these phe-
nomena can significantly disrupt a couple's sexual life and cause sub-
stantial misconceptions in human sexuality. The use of precise
definitions and terminologies may refine the differential diagnosis of
FE and SQ and facilitate further research in this field.
ACKNOWLEDGMENTS
The authors would like to thank Dr. Jan Balko from the Department
of Pathology and Molecular Medicine, Motol University Hospital, for
assisting with the figures and the guidance on the anatomical struc-
tures of the female genitalia. We would also like to thank Prof.
Miroslava Horáčková from the Department of Internal Medicine,
Motol University Hospital, for valuable comments on the urinary tract
function during sexual stimulation.
ORCID
Zlatko Pastor https://orcid.org/0000-0002-1425-5982
8PASTOR AND CHMEL
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How to cite this article: Pastor, Z., & Chmel, R. (2022). Female
ejaculation and squirting as similar but completely different
phenomena: A narrative review of current research. Clinical
Anatomy,110. https://doi.org/10.1002/ca.23879
10 PASTOR AND CHMEL
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Benign prostatic hyperplasia (BPH) is among the commonest urological abnormality affecting the aging male. The cause of the increase in prostatic volume is multifactorial, but current research has implicated hormonal aberrations. Clinical assessment of the patient is integral to determining the optimal treatment strategy. Exclusion of prostatic cancer and complications of BPH are critical prior to the commencement of conservative and non-invasive strategies. Recently, the introduction of pharmaceutical agents has changed the landscape of management of BPH. Alpha-blockers, 5-alpha reductase inhibitors and now phosphodiesterase-5 inhibitors provide significant symptomatic improvement for BPH, particularly when used in combination. Invasive surgical therapies remain the gold standard for refractory and complicated BPH disease. Advances in technology have provided new methods to perform prostatectomy including: bipolar resection, laser resection, ablation, enucleation or vaporization. Newer, minimally invasive measures have been introduced in an attempt to limit patient morbidity, specifically operative complications, sexual and urinary function. While results are promising, these emerging therapies have limited long-term data. The purpose of the current chapter is to provide an overview of the current knowledge of benign prostatic hyperplasia. For complete coverage of this and all related areas of Endocrinology, please visit our FREE web-book, www.endotext.org. .
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The article consist of six sections written by separate authors that review female genital anatomy, the physiology of female sexual function, the pathophysiology of female sexual dysfunction but excluding hormonal aspects. Aim: To review the physiology of female sexual function and the pathophysiology of female sexual dysfunction especially since 2010 and to make specific recommendations accordng to the Oxford Centre for evidence based medicine (2009) "levels of evidence" wherever relevant. Conclusion: Recommendations were made for particular studies to be undertaken especially in controversial aspects in all six sections of the reviewed topics. Despite numerous laboratory assessments of female sexual function, genital assessments alone appear insufficient to characterise fully the complete sexual response.
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A major area of continued controversy and debate among sex researchers, gynecologists and sex therapists has been and continues to be the question of the phenomenon known as "female ejaculation." The current study was an exploratory research experiment designed to provide information about this issue by catheterizing seven women, who reported that they regularly expelled fluid during sensual and/or sexual arousal. Evidence from various studies of live subjects, involving in total less than fifty women, has shown, at least in these subjects, that what was being considered was a urethral expulsion. However, with the total number of women studied being so small, it was impossible to rule out the possibility that some woman somewhere is expelling fluid other than through the urethra. While the current experiment, based upon a review of previous studies, focused on the nature, composition and source of female urethral expulsions during sensual arousal, this researcher was certainly open to observing, capturing and analyzing any expulsions other than from the urethra. With catheterization, the bladder could be isolated from the urethra so that it could be reliably determined which fluids came from which area. The fluids obtained could then be analyzed for their individual composition, having lessened the possibility that they had been mixed in the urethra. The entire experiment was videotaped with a medical doctor and/or a registered nurse present at all times. The overall environment was designed to be as comfortable and natural as possible for the women subjects in order to increase the probability that there would be fluid to be collected. The primary conclusion from the experiment was that almost all the fluid expelled from these seven women unquestionably came from their bladders. Even though their bladders had been drained, they still expelled from 50 ml to 900 ml of fluid through the tube and into the catheter bag. The only reasonable conclusion would be that the fluid came from a combination of residual moisture in the walls of the bladder and from post draining kidney output. There was also a consistency of results that showed a greatly reduced concentration of the two primary components of urine, urea and creatinine, in the expelled fluid. A review of previous literature leads to an inference that it is possible that the expelled fluid is an altered form of urine and that there may be a chemical process that goes on during sexual stimulation and excitement that changes the composition of urine. On four occasions the research team saw evidence of milky-white, mucous-like emissions from the urethra outside of the catheter tube. Although three of those emissions were recorded by the video cameras, the research team was only able to capture a small portion of the fluid for laboratory analysis. An objective reading of the previous literature indicated the possibility of such an emission from the urethral glands and ducts. In the past, the assumption has been that female urethral expulsions during sensual and/or sexual activity originated either in the bladder or from the urethral glands and ducts. The current study, which documented expulsions originating in the bladder, also indicated the possibility that, in some women, there may also be an emission from the urethral glands and ducts. That possibility seems promising enough to encourage future researchers to employ methodology similar to this study to resolve this age old controversy.
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IntroductionDuring sexual stimulation, some women report the discharge of a noticeable amount of fluid from the urethra, a phenomenon also called “squirting.” To date, both the nature and the origin of squirting remain controversial. In this investigation, we not only analyzed the biochemical nature of the emitted fluid, but also explored the presence of any pelvic liquid collection that could result from sexual arousal and explain a massive fluid emission.Methods Seven women, without gynecologic abnormalities and who reported recurrent and massive fluid emission during sexual stimulation, underwent provoked sexual arousal. Pelvic ultrasound scans were performed after voluntary urination (US1), and during sexual stimulation just before (US2) and after (US3) squirting. Urea, creatinine, uric acid, and prostatic-specific antigen (PSA) concentrations were assessed in urinary samples before sexual stimulation (BSU) and after squirting (ASU), and squirting sample itself (S).ResultsIn all participants, US1 confirmed thorough bladder emptiness. After a variable time of sexual excitation, US2 (just before squirting) showed noticeable bladder filling, and US3 (just after squirting) demonstrated that the bladder had been emptied again. Biochemical analysis of BSU, S, and ASU showed comparable urea, creatinine, and uric acid concentrations in all participants. Yet, whereas PSA was not detected in BSU in six out of seven participants, this antigen was present in S and ASU in five out of seven participants.Conclusions The present data based on ultrasonographic bladder monitoring and biochemical analyses indicate that squirting is essentially the involuntary emission of urine during sexual activity, although a marginal contribution of prostatic secretions to the emitted fluid often exists. Salama S, Boitrelle F, Gauquelin A, Malagrida L, Thiounn N, and Desvaux P. Nature and origin of “squirting” in female sexuality. J Sex Med **;**:**–**.