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Seminal vesicles

The seminal vesicles are a pair of coiled, tubular glands in the male reproductive system, located in the pelvis posterior to the urinary bladder base, superior to the rectum, and anterior to the prostate gland, from which they are separated by Denonvilliers' fascia.^[1] Each measures approximately 3 to 5 cm in length and 1 cm in diameter; when uncoiled, up to 10 to 15 cm in length, consisting of mucosal, muscular, and adventitial layers, with the mucosa lined by pseudostratified columnar epithelium that secretes fluid.^[1] Their ducts join the ampulla of the vas deferens to form the ejaculatory ducts, which empty into the prostatic urethra at the verumontanum.^[1] Functionally, the seminal vesicles produce a viscous, slightly alkaline fluid that comprises about 70% of semen volume, containing fructose for sperm energy, prostaglandins to enhance sperm motility and viability, semenogelin proteins for post-ejaculatory coagulation, enzymes, vitamin C, and other substances that create a protective and nutritious environment for spermatozoa during transport and fertilization.^[1] Secretion is regulated by parasympathetic nerves for glandular activity and sympathetic nerves for muscular contraction during ejaculation, ensuring fluid release coincides with sperm emission.^[1] This contribution is vital for male fertility, as deficiencies in seminal vesicle function can impair semen quality, sperm survival, and reproductive success.^[2] Embryologically, the seminal vesicles develop from the mesonephric (Wolffian) ducts around the 10th week of fetal life, under the influence of testosterone, in conjunction with the epididymis and vas deferens.^[1] Blood supply derives from the middle and inferior vesical arteries, with venous drainage via the vesical plexus to the internal iliac veins, and lymphatic drainage to the internal and external iliac nodes.^[1] Clinically, the seminal vesicles are involved in conditions such as congenital cysts, agenesis (often linked to renal or vas deferens abnormalities or cystic fibrosis), infections, stones, or neoplasms, which may cause pelvic pain, infertility, or hematospermia, though many remain asymptomatic.^[1] They are often affected in prostate cancer, with surgical removal during radical prostatectomy potentially leading to anejaculation, though nerve-sparing techniques aim to preserve function.^[1]

Anatomy

Gross anatomy

The seminal vesicles are a pair of convoluted, sac-like glandular structures in the male reproductive system, located posterior to the urinary bladder and superior to the prostate gland. Each vesicle measures approximately 5 cm in length and 3 cm in diameter when distended, though if uncoiled, it can extend up to 10-15 cm. They exhibit a pyramidal form, consisting of a broad body and a narrow excretory duct that joins the ampulla of the vas deferens to form the ejaculatory duct, which then penetrates the prostate to open into the prostatic urethra.^[3]^[4]^[5] In terms of anatomical relations, the seminal vesicles lie anterior to the rectum, separated by the rectovesical pouch and Denonvilliers' fascia, and are positioned lateral to the ampulla of the vas deferens and medial to the ureters. Their superior aspect is covered indirectly by the peritoneum of the rectovesical pouch, while inferiorly and anteriorly they relate to the base of the bladder and the prostate. Laterally, they are adjacent to the prostatic venous plexus.^[3]^[4]^[6] The blood supply to the seminal vesicles is primarily derived from branches of the inferior vesical artery and the middle rectal artery, both arising from the internal iliac artery. Venous drainage occurs via tributaries that join the prostatic venous plexus, ultimately draining into the internal iliac veins. Innervation is provided by the inferior hypogastric plexus, which carries both sympathetic fibers from the superior hypogastric plexus and parasympathetic fibers from the pelvic splanchnic nerves, facilitating functions such as glandular secretion and smooth muscle contraction. Lymphatic drainage follows the vascular supply, emptying into the internal iliac lymph nodes.^[3]^[5]^[6]

Microscopic anatomy

The seminal vesicles are composed of a mucosal layer lined by a pseudostratified columnar epithelium consisting of principal secretory cells and supportive basal cells, an underlying lamina propria of loose connective tissue, and concentric layers of smooth muscle for contraction.^[1]^[7] The principal cells are tall columnar cells responsible for fluid secretion, featuring microvilli on their apical surface, abundant rough endoplasmic reticulum, and secretory granules, while basal cells are small, round cells lying on the basement membrane that provide structural support.^[8] Occasional goblet cells are present within the epithelium, contributing to mucin production.^[1] The glandular architecture is highly branched and tubuloalveolar, forming a complex of coiled tubules and alveolar (acinar) outpouchings with extensive mucosal folds that maximize the secretory surface area.^[7]^[9] These structures empty into a central lumen, creating an irregular, pouch-like interior without a distinct submucosa; instead, the mucosa transitions directly to the muscularis.^[1] The surrounding stroma comprises fibromuscular connective tissue rich in elastic fibers, interspersed with autonomic nerve endings that innervate the smooth muscle layers—inner circular and outer longitudinal—for coordinated expulsion during ejaculation.^[10]^[11] The outer adventitia is a thin layer of loose areolar connective tissue that blends seamlessly with adjacent pelvic structures, lacking a serosal covering.^[1] Epithelial cell height and secretory activity vary with hormonal influences, particularly androgens like testosterone, which maintain tall columnar morphology in humans; reductions occur in hypogonadal states, leading to epithelial flattening.^[10]^[12]

Embryological development

The seminal vesicles originate from the mesonephric (Wolffian) ducts during early fetal development, specifically as lateral evaginations from the caudal portion of these ducts near their junction with the urogenital sinus.^[1] These structures arise in the male embryo under the influence of androgens, differentiating alongside other Wolffian duct derivatives such as the epididymis, vas deferens, and ejaculatory ducts.^[13] In the absence of a Y chromosome and subsequent male hormonal signaling, the mesonephric ducts regress, preventing seminal vesicle formation.^[1] Development begins around the 10th week of gestation, when the seminal vesicles sprout as outpouchings from the distal mesonephric ducts.^[1] By week 13 (crown-rump length approximately 80 mm), these buds elongate and form initial sacculations, progressing to 3 distinct diverticula per vesicle by week 14.^[14] Branching morphogenesis continues, with 3-8 sacculations evident by week 19 (crown-rump length 170 mm), and the structures approaching their adult configuration with 9-12 diverticula by week 25 (crown-rump length 220 mm).^[14] Toward late gestation, the seminal vesicles fuse with the ampulla of the vas deferens to form the ejaculatory ducts, completing the basic architectural framework.^[1] Hormonal regulation is critical, with fetal testosterone produced by Leydig cells in the testes inducing differentiation through androgen receptors in the mesenchyme and epithelium.^[13] This androgen-dependent mesenchymal-epithelial interaction drives outgrowth and branching, while anti-Müllerian hormone from Sertoli cells suppresses paramesonephric (Müllerian) duct remnants to prevent female structure formation.^[1] The glands remain immature until puberty, when further androgen surges promote functional maturation.^[13] Congenital anomalies of the seminal vesicles stem from disruptions in mesonephric duct development and are often associated with ipsilateral renal agenesis or other Wolffian duct malformations.^[1] Unilateral or bilateral agenesis is rare but can occur in conjunction with congenital bilateral absence of the vas deferens (CBAVD), frequently linked to mutations in the CFTR gene on chromosome 7p, leading to obstructive azoospermia.^[1] Other anomalies include hypoplasia, cysts, or fusion/duplication, typically identified through imaging in cases of infertility or urinary tract issues.^[14]

Function

Composition of secretions

The secretions of the seminal vesicles constitute approximately 65-70% of the total semen volume in humans, forming a viscous, alkaline fluid with a pH ranging from 7.2 to 8.0 that helps neutralize the acidic environment of the vagina.^[15]^[16] This fluid is rich in several key biochemical components essential for sperm function. Fructose, present at concentrations of 2-5 mg/mL, serves as the primary energy source for spermatozoa via glycolysis.^[17] Prostaglandins, abundant in the secretion, enhance sperm motility and induce uterine contractions to facilitate sperm transport.^[18] Semenogelin proteins, secreted in high amounts, contribute to the formation of a coagulum immediately after ejaculation, temporarily immobilizing sperm at the cervical os.^[16] Additional components include flavins, which may support redox reactions in the seminal environment, and citrate, which acts as a buffer and metabolic intermediate.^[19]^[20] The secretory process involves principal epithelial cells in the seminal vesicle lining, which release material through an apocrine-like mechanism involving blebbing of the apical cytoplasm.^[21] This secretion is tightly regulated by androgens, particularly testosterone, which maintain glandular function and protein synthesis via androgen receptor signaling.^[22] Each gland produces approximately 1-2 mL of fluid daily under normal conditions, accumulating for release during ejaculation.^[23] Recent proteomic analyses post-2020 have identified over 500 proteins in seminal vesicle-derived fluid, including antimicrobial zinc-binding proteins such as those derived from semenogelins, which exhibit bactericidal activity against pathogens in the reproductive tract.^[24]^[25] Additionally, studies have highlighted the presence of polyamines like spermine and spermidine, which stabilize sperm DNA structure by binding to nucleic acids and promoting compact conformations resistant to damage.^[26] Updated metabolomics research from 2022 emphasizes the role of fructose metabolism in seminal vesicle function, linking reduced fructose levels to infertility due to impaired energy provision for sperm.^[27]

Physiological role

The seminal vesicles contribute the majority of the seminal plasma volume, approximately 60-70%, which is essential for semen formation during ejaculation. This viscous, alkaline fluid mixes with spermatozoa from the testes and secretions from other accessory glands to create semen, facilitating sperm transport through the male reproductive tract, providing nutritional support via energy substrates, and offering protection against oxidative stress and acidic environments during transit to the female reproductive tract.^[1] Key components of the seminal vesicle secretions play critical roles in sperm function. Fructose, produced in high concentrations by the vesicular epithelium, serves as the primary energy source for sperm glycolysis, powering flagellar motility and enabling progressive movement essential for fertilization. Prostaglandins, predominantly synthesized in the seminal vesicles, promote sperm capacitation and hyperactivation in the female tract by modulating calcium influx and membrane fluidity, and induce uterine contractions to facilitate sperm transport. Semenogelin II, a major protein secreted by the vesicles, initiates the coagulation of semen upon ejaculation, forming a temporary gel matrix in the female genital tract that stabilizes sperm positioning; this coagulum subsequently liquefies through proteolytic action, releasing motile sperm for ascent toward the oocyte.^[28]^[29] Secretion from the seminal vesicles is under androgen-dependent hormonal control, primarily testosterone and its metabolite dihydrotestosterone (DHT), which drive glandular development and secretory activity peaking at puberty. Neural regulation via sympathetic innervation triggers vesicular contraction and fluid expulsion during sexual arousal and ejaculation, ensuring synchronized contribution to semen. In terms of fertility, the seminal vesicles are vital for maintaining normal semen viscosity, volume, and biochemical milieu; their congenital absence or dysfunction results in aspermia or severe oligospermia, leading to infertility due to inadequate sperm support and delivery.^[22]^[1]^[30] Recent studies highlight the seminal vesicles' role in immune modulation through seminal plasma components, including extracellular vesicles that interact with female immune cells to induce tolerance toward paternal antigens, reducing inflammation and enhancing implantation success. For instance, seminal plasma immunosuppressants, such as transforming growth factor-beta and prostaglandin E, derived largely from vesicular secretions, dampen T-cell responses in the female reproductive tract, preventing rejection of spermatozoa and supporting early embryonic development.^[31]^[32]

Clinical significance

Associated diseases

Congenital anomalies of the seminal vesicles, such as agenesis or cysts, are rare developmental abnormalities that often occur in association with ipsilateral renal agenesis or Müllerian duct remnants, collectively known as Zinner syndrome. These conditions arise from disruptions in Wolffian duct embryogenesis and are estimated to account for approximately 2% of male infertility cases due to obstructive azoospermia or severe oligospermia.^[30] Affected individuals typically present with infertility as the primary manifestation, alongside low semen volume and acidic pH from absent seminal contributions.^[33] Seminal vesiculitis, an inflammatory condition of the seminal vesicles, is predominantly bacterial in etiology and frequently occurs as a secondary complication of prostatitis or urinary tract infections.^[34] Common pathogens include Chlamydia trachomatis and, in endemic regions, Mycobacterium tuberculosis or Schistosoma species, leading to acute or chronic presentations with symptoms such as dysuria, hematuria, pelvic or lower abdominal pain, and painful ejaculation.^[35] Epidemiologically, chronic bacterial seminal vesiculitis coexists in a significant proportion of chronic prostatitis cases, with inflammatory changes commonly observed via transrectal ultrasound.^[36] This association underscores its role in persistent genitourinary symptoms and potential fertility impairment through altered seminal fluid composition.^[37] Neoplastic involvement of the seminal vesicles is uncommon as a primary site but frequently results from local extension of prostate adenocarcinoma, classified as T3b disease in staging systems.^[38] Primary seminal vesicle adenocarcinoma is exceedingly rare, with delayed diagnosis contributing to a poor prognosis and high mortality within three years.^[39] Additionally, calculi formation within the seminal vesicles can develop due to secretory stagnation, often presenting with recurrent hematospermia and requiring imaging for confirmation.^[40] Functional disorders, including seminal vesicle hypoplasia, are associated with hypogonadism, where androgen deficiency impairs glandular development and secretion.^[41] This leads to reduced ejaculate volume (hypospermia) and asthenospermia, as the seminal vesicles normally contribute 40-80% of semen volume and essential motility factors like fructose.^[42] In such cases, low testosterone levels directly correlate with diminished vesicular output, exacerbating infertility.^[43] Research has highlighted links between seminal vesicle pathology and systemic conditions. Metabolic syndrome and diabetes mellitus impair vesicular secretion quality through hyperglycemia-induced oxidative stress, resulting in decreased seminal fluid volume, altered fructose levels, and reduced sperm motility.^[44] Studies indicate that microbiome dysbiosis in semen may contribute to infertility, with altered bacterial communities observed in men with abnormal semen parameters.^[45] Genetic predispositions, such as HOXB13 mutations (e.g., G84E variant), increase susceptibility to prostate cancer with seminal vesicle invasion, while also disrupting normal prostate and vesicular development.^[46] Furthermore, post-COVID-19 inflammatory sequelae have been implicated in persistent male reproductive inflammation, potentially affecting seminal vesicle function via elevated cytokines and tissue damage.^[47]

Diagnostic and therapeutic approaches

Diagnosis of seminal vesicle disorders typically begins with non-invasive imaging techniques to assess structural abnormalities such as cysts, inflammation, or calculi. Transrectal ultrasound (TRUS) serves as the initial modality of choice due to its accessibility and ability to visualize the seminal vesicles in detail, particularly for detecting cysts and inflammatory changes.^[48] For more precise anatomical delineation and staging of malignancies involving the seminal vesicles, magnetic resonance imaging (MRI), especially high-field 3T MRI, provides superior soft-tissue contrast and multiplanar imaging, enabling accurate assessment of tumor extension and invasion. Computed tomography (CT) scans are particularly useful for identifying calculi within the seminal vesicles, as they offer high-density resolution for stone detection and associated complications like obstruction. Semen analysis plays a crucial role in indirectly evaluating seminal vesicle function by measuring parameters influenced by vesicular secretions, including ejaculate volume (typically 60-70% contributed by the vesicles), pH (alkaline due to vesicular input), and fructose levels (a marker of vesicular activity), with reductions suggesting hypofunction or obstruction. For more definitive assessment in cases of suspected ductal anomalies or persistent symptoms, invasive procedures such as vesiculography—performed via catheterization of the ejaculatory duct or vas deferens—allow contrast injection to outline the vesicular lumen and identify strictures or reflux.^[49] Biopsy, often guided by TRUS or MRI, is employed when malignancy is suspected, providing histopathological confirmation through transrectal or transperineal approaches, though it carries risks of infection or bleeding. Therapeutic approaches to seminal vesicle disorders are tailored to the underlying pathology, prioritizing conservative management when possible. Infections, such as seminal vesiculitis, are primarily treated with antibiotics like fluoroquinolones (e.g., ciprofloxacin), often administered for 2-4 weeks.^[36] For cysts or abscesses causing obstruction or pain, surgical interventions include drainage via percutaneous or transrectal aspiration, or resection through minimally invasive techniques such as laparoscopic or robotic-assisted procedures, which have reduced recovery times and complication rates compared to open surgery. Calculi are managed with endoscopic aspiration or holmium laser lithotripsy, offering stone fragmentation with minimal tissue damage and success rates exceeding 90% in accessible cases. In the context of fertility impairment due to seminal vesicle hypofunction, assisted reproductive technologies like in vitro fertilization (IVF) combined with intracytoplasmic sperm injection (ICSI) are employed to bypass vesicular contributions to semen quality, achieving pregnancy rates of 30-50% per cycle in affected couples.^[50] Additionally, hormone replacement therapy with testosterone is indicated for associated hypogonadism, restoring vesicular secretory function and improving semen parameters in up to 70% of cases. Recent advancements have enhanced diagnostic precision, including expanded use of 3T MRI for early cancer detection. Therapeutic options have also evolved, with robotic surgery enabling precise minimally invasive resections for complex cysts, reducing operative times and hospital stays.

Comparative anatomy

In mammals

Seminal vesicles are present in most mammals, including humans, bulls, and rodents, where they serve as paired accessory glands that contribute 50–80% of the total semen volume through their alkaline, protein-rich secretions. These glands are essential for providing the bulk of seminal plasma, which supports sperm motility and viability across species. In ruminants such as bovines, the seminal vesicles are notably larger and more complex, exhibiting a compact, lobulated structure with multiple lobes that enhance secretory capacity tailored to high-volume ejaculates. By contrast, in rodents like mice, the glands are smaller and produce relatively fructose-poor secretions, reflecting adaptations to lower semen volumes and different metabolic demands for sperm energy. Functional variations among mammals highlight species-specific adaptations in seminal vesicle secretions. In primates, high concentrations of prostaglandins produced by the glands modulate the female immune response, promoting embryo implantation by inducing tolerance and reducing inflammation at the uterine site. In equines, polyamines such as spermine and spermidine dominate the seminal plasma proteome, enhancing sperm longevity by protecting against oxidative stress and supporting extended viability in the female tract. The development of seminal vesicles is conserved across mammals through androgen-dependent pathways, ensuring glandular differentiation during embryogenesis. However, gland size shows evolutionary correlation with mating strategies, being larger in promiscuous species to counter sperm competition via increased seminal fluid investment.

In other vertebrates

In non-mammalian vertebrates, structures analogous to seminal vesicles vary widely, reflecting adaptations to diverse reproductive strategies such as external versus internal fertilization. These glands, when present, typically derive from mesodermal tissues associated with the Wolffian (mesonephric) ducts, contributing fluids that aid sperm maturation, storage, or protection. However, they are absent in the most basal vertebrates, the cyclostomes (lampreys and hagfishes), which lack dedicated genital ducts altogether; instead, mature sperm are released directly into the coelomic cavity for external fertilization.^[51]^[52]^[53] Among gnathostomes, chondrichthyans (sharks, rays, and chimaeras) possess functional analogs in the form of Leydig glands, which are branched tubular structures derived from the anterior kidney region. These glands empty their secretions—primarily a matrix rich in proteins and mucins—directly onto the epididymis and ductus deferens, facilitating sperm storage and nourishment in species with internal fertilization. In contrast, teleost fish (bony fish) often feature true seminal vesicles or testicular accessory glands, which are lobular outpouchings along the spermatic ducts that produce viscous fluids containing sialoglycoproteins and mucins to enhance sperm motility and form spermatophores during spawning. For example, in the grass goby (Zosterisessor ophiocephalus), these glands secrete seasonally to support external fertilization in marine environments.^[54]^[55]^[56] Amphibians exhibit seasonal glandular outpouchings in the cloaca that function similarly to seminal vesicles, storing sperm and producing seminal fluid components essential for spermatophore formation and transfer. In anurans like the common frog (Rana temporaria), these structures develop post-metamorphosis from mesonephric derivatives, aiding internal fertilization in terrestrial breeding. Reptiles and birds, however, generally lack well-developed seminal vesicles; instead, semen storage and fluid production occur via rudimentary cloacal glands or sperm storage tubules. In reptiles such as lizards, these cloacal structures secrete minimal fluids for sperm maintenance during prolonged storage, while in birds, the cloacal protuberance facilitates direct sperm transfer via "cloacal kiss," with glandular secretions limited to vas deferens-associated tissues. These variations underscore evolutionary ties to fertilization modes, with more complex glands emerging in lineages favoring internal insemination.^[57]^[58]^[59] Recent phylogenomic analyses of chordate genomes have traced homologs of reproductive glandular tissues to ancient deuterostome ancestors, suggesting that mesodermally derived secretory structures predated vertebrate innovations but diversified with the evolution of gonadal ducts. For instance, conserved gene modules involved in glandular development appear in basal chordates like amphioxus, implying a shared origin for fluid-producing accessories across vertebrates, though specific seminal vesicle homologs remain elusive in non-gnathostome lineages.^[60]^[61]

History

Discovery and early descriptions

The earliest known references to structures akin to the seminal vesicles appear in the writings of the Roman physician Galen during the 2nd century AD, where he described "spermatic vessels" as part of the male reproductive tract, though these accounts were largely inaccurate, derived from animal dissections, and conflated with other vascular elements. The first precise anatomical identification in humans occurred in 1521, when Italian anatomist Berengario da Carpi documented the paired glands during dissections and coined the term vesiculae seminales, distinguishing them from the prostate and emphasizing their vesicular appearance near the bladder base.^[62] This identification was overlooked by Andreas Vesalius in his seminal 1543 anatomical atlas De humani corporis fabrica, underscoring the foundational role of Berengario's earlier work.^[62] In the 1770s, Scottish surgeon John Hunter further clarified their function in mammals, demonstrating through comparative dissections that the seminal vesicles contribute fluid to semen rather than storing sperm, thereby correcting a prevalent pre-19th-century misconception that portrayed them as reservoirs for spermatozoa.^[63]

Evolution of understanding

In the mid-19th century, histological studies advanced the understanding of seminal vesicle structure and function. Albert von Kölliker, through microscopic examination detailed in his 1854 Manual of Human Histology, confirmed the glandular nature of the seminal vesicles, describing their epithelial lining and secretory capabilities, which established them as accessory glands contributing to seminal fluid rather than mere storage organs. This work built on earlier anatomical observations by providing cellular-level evidence of their exocrine role. Early 20th-century biochemical analyses revealed key components of seminal vesicle secretions. In the 1940s, Thaddeus Mann identified fructose as a major carbohydrate in mammalian semen, primarily derived from seminal vesicle contributions, highlighting its role in providing energy for spermatozoa motility.^[64] Concurrently, the 1930s marked the elucidation of hormonal regulation; experiments by Carl R. Moore and Dorothy Price demonstrated that testosterone implants in castrated rats restored seminal vesicle weight and secretory activity, establishing androgens as essential for maintaining glandular development and function. By the 1960s, electron microscopy provided ultrastructural insights; Helen Wendler Deane's studies revealed the detailed morphology of principal and basal cells, including secretory granules and smooth muscle layers, underscoring the vesicles' apocrine secretion mechanism. Molecular and genomic investigations in the late 20th century shifted focus to genetic underpinnings. In the 1990s, researchers cloned and characterized the semenogelin genes (SEMG1 and SEMG2) from seminal vesicle cDNA libraries, identifying them as the primary proteins forming the seminal coagulum and revealing their chromosomal location on 20q13, with implications for liquefaction and fertility.^[65] Entering the 2000s, proteomic approaches mapped the diverse protein repertoire of seminal vesicle secretions; a landmark 2006 study identified over 900 proteins in human seminal plasma, including semenogelins, prostate-specific antigen, and antioxidants, providing a comprehensive catalog that linked specific proteins to sperm protection and motility enhancement.^[66] Post-2020 research has integrated advanced tools like CRISPR/Cas9 to probe gene functions and environmental impacts. Additionally, investigations into reproductive toxicology have linked endocrine disruptors, such as bisphenol A and phthalates, to seminal vesicle dysfunction; recent analyses as of 2023 show these chemicals alter androgen signaling and secretory profiles, contributing to reduced semen quality and fertility declines observed in human populations.^[67]

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These studies suggested a negative impact of DM on erectile and ejaculation function, as well as a reduction in semen volume, sperm counts, sperm motility and ...<|separator|>
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Semen microbiota are dramatically altered in men with abnormal ...
Jan 11, 2024 · Advances in our understanding of the semen microbiome may contribute to potentially new therapeutic avenues for correcting impairments in sperm ...Microbiome Community... · Results · DiscussionMissing: vesiculitis | Show results with:vesiculitis
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HOXB13 mutations and binding partners in prostate development ...
Hoxa-13 gene mutation results in abnormal seminal vesicle and prostate development. ... HOXB13 is a susceptibility gene for prostate cancer: results from ...
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A short review of male genito-urinary lesions caused by coronavirus ...
Jun 27, 2022 · COVID-19 has considerable effects on the kidneys, testes, vas deferens, epididymis, seminal vesicles, prostate, and penis.Missing: post- vesiculitis
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Detecting diseases of neglected seminal vesicles using imaging ...
Transrectal ultrasound (TRUS) should be the first-line modality for genitourinary tract imaging because it is minimally an invasive imaging modality, ...
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Transrectal US-guided seminal vesicle aspiration in the diagnosis of ...
TRUS-guided seminal vesicle aspiration can be used in conjunction with TRUS to confirm the diagnosis pre-operatively, especially in patients with seminal ...<|control11|><|separator|>
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Seminal vesicles ultrasound features in a cohort of infertility patients
At transrectal ultrasound, SV have a typical 'bow-tie' appearance in a transverse scan and an oval configuration. Their echo-texture is usually homogeneous and ...
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Gamete-exporting organs of vertebrates: dazed and confused
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Regardless of whether a vertebrate develops gonads capable of making ova or sperm, the gonads arise from the genital ridge, specifically as mesoderm with ...
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Seminal Vesicle - an overview | ScienceDirect Topics
The capacity of each seminal vesicle is approximately 2 ml, which contributes about 70% of the ejaculate volume. During the emission phase of ejaculation, sperm ...
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Reproductive Anatomy of Chondrichthyans: Notes on Specimen ...
Jun 25, 2021 · The Leydig gland is adjacent to the ductus deferens onto which it empties its contents, as well as onto the epididymis. The gland, formed by the ...
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7. Reproductive biology
Leydig glands are a series of branched tubular glands that secrete seminal fluids into the epididymis and ductus deferens. The alkaline gland of batoids may ...
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The seminal vesicles of the male grass goby,Zosterisessor ...
The seminal vesicles are accessory glands of the male reproductive system which produce sialoglycoproteins during the spawning period.
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A review of the reproductive system in anuran amphibians
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[PDF] Sperm Competition and the Anuran Seminal Vesicles
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The Post-Metamorphic Development of the Kidney, and the Development of the Vasa Efferentia and Seminal Vesicles in Rana Temporaria Available. Peter Gray.
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Molecular evidence for pre-chordate origins of ovarian cell types ...
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Improved Understanding of the Role of Gene and Genome ...
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[PDF] Marcello Malpighi (1628-1694): Pioneer of microscopic anatomy ...
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A male mole, caught and killed in autumn - RCSEng
Apr 30, 2025 · In this work, he refutes the commonly held idea that the seminal vesicles act as “reservoirs of the semen” while asserting that they are still “ ...
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Sugar of Human Semen | Nature
that of the bull, ram and boar were under investigation—has been identified as d-fructose.Missing: fluid | Show results with:fluid
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The genes for semenogelin I and II, the major protein constituents of the human seminal fluid, have been characterized by three overlapping clones in ...
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Large-scale and high-confidence proteomic analysis of human ...
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Endocrine disrupting chemicals and male fertility - Frontiers
Endocrine disrupting chemicals (EDCs) exposure may affect male fertility at multiple levels, from sperm production and quality to the morphology and histology ...