SEARCH · PubMed Health

Results for “Rete Testis”

Explore indexed PubMed citations for clinical trials, systematic reviews and public health research. Read source abstracts and follow each citation to its original PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 181 records · Page 10Linked to original sources

PubMed1999

Postnatal differentiation of the ductus deferens, tail of the epididymis, and distal body of the epididymis in goats occurs independently of rete testis fluid.

Observations from extratesticular rete-ligated, mature goats indicated that epithelial morphology in the tail of the epididymis can be maintained without any input from testicular fluid (Goyal et al., Acta Anat., 1994;150: 127-135). Hence, the objective of this study was to determine whether the tail of the epididymis and/or other regions of the male excurrent ducts can differentiate prior to the appearance of lumen in the seminiferous tubules, which is an indicator for the onset of seminiferous tubular fluid secretion. Based on age and scrotal circumference (SC), 20 male goats were divided into four groups of five animals each: 1-4 weeks (SC, 6.5-7.5 cm), 7-10 weeks (SC, 8.5-11.0 cm), 12-15 weeks (SC, 11.0-14.0 cm), and 15-25 weeks (SC, 16.0-19.0 cm). Tissues were collected from the testis, six regions of the epididymis (proximal, middle and distal head; proximal and distal body; and tail), and the ductus deferens, and were processed for light and electron microscopic examination. Changes in epithelial height and cytological features associated with absorption (microvilli, pinocytotic and coated vesicles) and protein secretion (RER, Golgi body) were used as markers for differentiation. Differentiation of all of these features was comparable to that observed in the 15-25-week-old animals in the ductus deferens by > or = 1 week, in the tail of the epididymis by > or = 7 weeks, in the distal body of the epididymis by > or = 12 weeks, and in the proximal body of the epididymis and all three regions of the head of the epididymis by > or = 15 weeks. Seminiferous tubules developed lumens between 12 and 15 weeks. In conclusion, epithelial differentiation in the ductus deferens, tail of the epididymis, and distal body of the epididymis follows a time-dependent, spatial, ascending order and is achieved before lumen formation in the seminiferous tubules. Conversely, epithelial differentiation in all three regions of the head and the proximal body of the epididymis occurs simultaneously and after lumen formation in the seminiferous tubules.

Age Factors↗

PubMedDate not supplied

Polyorchidism and rete testis adenoma: ultrasound and MR findings.

Polyorchidism is an uncommon congenital anomaly. It is associated with an increased frequency of testicular malignancy, cryptorchidism, inguinal hernia, and torsion. Sonography may be used to confirm the clinically suspected diagnosis. We present a case of polyorchidism in which a rete testis adenoma was present in one of the testicles. Sonographic and magnetic resonance findings are illustrated.

Adenoma↗

PubMed1993

Evidence for a protein-like factor from "rete testis" fluid that suppresses luteinizing hormone-releasing hormone (LHRH) pulses (LHRH statin): a new hormonal activity?

Signals that modulate LH-releasing hormone (LHRH) pulse frequency are fundamental mechanisms for regulating important reproductive processes. Gonadal steroids are presently considered to account for the entire gonadal feedback mechanism that modulates LHRH secretion. However, we have previously suggested that a testicular protein(s) present in charcoal-treated rete testis fluid (ctRTF) can suppress LH pulsatility in the ram. The present experiments were aimed at determining whether the disappearance of LH pulses induced by ctRTF administration implicate a hypothalamic or a pituitary site of action. Thus, we have examined the effects of ctRTF peripheral administration on 1) the LH response to LHRH, 2) LHRH portal blood levels, and 3) LHRH content in hypothalamic tissue. Finally, the effects of ctRTF administered into the third ventricle on plasma LH levels were assessed. The present results show that a testicular protein(s) is able to suppress LHRH pulse frequency without affecting amplitude and without any effect on the LH response to LHRH (LHRH Statin). The observation that an active dose administered by the intracerebroventricular route is 0.0005 the active dose needed by the peripheral route reinforces this evidence. These data lead to the new concept that the testicular signals that govern LHRH pulse frequency may be not only steroids, but also proteins.

Animals↗

PubMedDate not supplied

The effect of estrogen administration in vivo on the elemental composition of the intraluminal fluids of the seminiferous tubules, rete testis, and epididymis of the rat.

The maturation of spermatozoa in the epididymis is dependent upon the presence of androgens. This study examined the effects of androgen suppression by estradiol valerate on the elemental composition of the intraluminal fluids of the testis and epididymis. In the fluid from the caput epididymidis, the concentrations of sodium (106.1 +/- 3.4 to 182.8 +/- 16.9 mmol/1, P less than 0.01) and chloride (16.5 +/- 2.2 to 79.3 +/- 10.8 mmol/1, P less than 0.01) rose after treatment with estradiol valerate. By contrast, this treatment reduced the concentrations of phosphorus (63.7 +/- 1.6 to 47.8 +/- 3.2 mmol/1, P less than 0.01), sulfur (18.4 +/- 1.0 to 10.8 +/- 1.0 mmol/1, P less than 0.01), calcium (0.93 +/- 0.09 to 0.50 +/- 0.07 mmol/1, P less than 0.01), and magnesium (2.21 +/- 0.41 to 0.76 +/- 0.16 mmol/1, P less than 0.01). In the distal cauda epididymidis, the concentration of chloride rose after treatment with estradiol valerate (24.4 +/- 1.7 to 54.9 +/- 3.9 mmol/1, P less than 0.01), but the concentrations of the other measured elements (sodium, potassium, phosphorus, calcium, magnesium, and sulfur) were not altered by estrogen treatment. In rete testis fluid the concentration of phosphorus fell (2.00 +/- 0.30 to 0.67 +/- 0.12 mmol/1, P less than 0.01), while that of calcium rose (0.66 +/- 0.15 to 1.55 +/- 0.21 mmol/1, P less than 0.01). Estrogen treatment did not appear to affect the elemental composition of seminiferous tubular fluid or serum. Therefore, estradiol valerate had a marked impact on the elemental composition of luminal fluid only in the caput epididymidis--where sperm maturation is initiated--and a minor effect on that of cauda epididymidal fluid--in which mature spermatozoa are stored.

Animals↗

PubMed1983

Influence of rete testis fluid on the metabolism of testosterone by cultured principal cells isolated from the proximal or distal caput of the rat epididymis.

Principle cells from 120 elutriations were used to improve procedures for culturing cells from the proximal or distal caput epididymidis. The criteria evaluated were metabolism of testosterone (T) to 5 alpha-reduced metabolites and cellular morphology after 6 days of culture. Isolated principal cells (greater than 90% viability) were cultured at 34 degrees C within a floating collagen matrix. Inclusion of transferrin or retinol in the culture medium increased the production of 5 alpha-reduced metabolites. Aggregation of principal cells before entrapment in the collagen matrix resulted in higher production of 5 alpha-reduced metabolites and more cells with a normal find structure than entrapment of dispersed cells in the matrix. Aggregated cells tended to form sheets or clusters, frequently arranged around a central lumen, with junctional complexes between adjacent cells. Cell polarity and morphologic features distinguishing principal cells from the proximal caput and distal caput epididymidis were retained. An average of 91% of the cells in aggregates were morphologically normal on Day 6 of culture in contrast to 5% for the single cells. Utilizing the improved culture procedure, we tested the hypothesis that ovine rete testis fluid (RTF) contains macromolecules which would aid in maintenance of a high rate of T metabolism. Principal cells were cultured in medium supplemented with 0 or 10% RTF, 10% ultrafiltrate of RTF (less than 10,000 daltons), or 10% newborn calf serum (NCS). Conversion of [3H]T to 5 alpha-reduced metabolites by cells from the proximal caput was twice that in cells from the distal caput on Day 6 of culture. Inclusion in the culture medium of 10% RTF or 10% NCS, but not 10% ultrafiltrate of RTF, increased (P less than 0.05) the production of 5 alpha-reduced metabolites by cells from both regions. We conclude that macromolecules in RTF or NCS are beneficial to maintenance of the ability to metabolize T by cultured principal cells, especially those from the proximal caput.

Androgen-Binding Protein↗

PubMed1970