Studies on the Structure and Formation during Spermatogenesis of the Sulfoglycerogalactolipid of Rat Testis

1974 ◽  
Vol 52 (8) ◽  
pp. 689-697 ◽  
Author(s):  
M. J. Kornblatt ◽  
A. Knapp ◽  
M. Levine ◽  
H. Schachter ◽  
R. K. Murray

Structural studies on the major glycolipid of rat testis have confirmed our earlier identification of this compound as a 1-O-alkyl-2-O-acyl-glyceryl-monogalactoside sulfate. The acyl and alkyl groups are predominantly palmitoyl and palmityl groups, respectively. The minor glycolipid found in the same tissue has been identified as the non-sulfated form of this glycolipid. Examination of the levels of the sulfoglycerogalactolipid in the testes of immature rats, hypophysectomized rats, and normal and sterile mice indicates that the majority of the compound is located in the germinal cells of the testis and that the primary spermatocytes are the earliest spermatogenic cells to contain high levels of the lipid. Galactolipid sulfotransferase also shows peak activity in the primary spermatocytes of rat testis.

1977 ◽  
Vol 9 (2) ◽  
pp. 159-167 ◽  
Author(s):  
J.A. Grootegoed ◽  
M.J. Peters ◽  
E. Mulder ◽  
F.F.G. Rommerts ◽  
H.J. Van Der Molen

1989 ◽  
Vol 108 (2) ◽  
pp. 367-375 ◽  
Author(s):  
M Abdullah ◽  
A L Kierszenbaum

We have found that the rat testis contains a cell surface galactosyl receptor that is antigenically related to the minor species of rat liver asialoglycoprotein receptor (ASGP-r) and has binding affinity for galactose coupled to agarose. In immunoblotting experiments, rat testis galactosyl receptor (RTG-r) is recognized by antiserum raised against the minor ASGP-r species of rat liver (designated rat hepatic lectin-2/3, RHL-2/3). Antiserum raised against the major species RHL-1 does not recognize an antigenic protein equivalent to RTG-r. Triton X-100-extracted rat liver and testes preparations fractionated by affinity chromatography on galactose-agarose and resolved by SDS-PAGE under reducing conditions, show that rat liver contains both the major (RHL-1) and minor (RHL-2/3) ASGP-r species whereas rat testis displays only a receptor species comigrating with RHL-2/3. RTG-r was present throughout testicular development. The receptor was found in seminiferous tubules, cultured Sertoli and spermatogenic cells, and epididymal sperm. Indirect immunofluorescent studies show RHL-2/3-like immunoreactivity on the surface of Sertoli cell, meiotic prophase spermatocytes, spermatids, and epididymal sperm. In spermatids and sperm, the immunoreactivity is restricted to the plasma membrane overlying the dorsal portion of the head. Because of RTG-r has galactose binding affinity, is present on surfaces of Sertoli and developing meiotic and postmeiotic spermatogenic cells, and overlies a region of the intact acrosome on epididymal sperm, RTG-r may have a role in spermatogenesis and in events leading to sperm-egg recognition.


1975 ◽  
Vol 64 (2) ◽  
pp. 337-347 ◽  
Author(s):  
CATHERINE A. WILSON ◽  
C. E. HORTH ◽  
A. McNEILLY ◽  
P. G. McDONALD

SUMMARY Serotonin (50 and 100 mg/kg), given subcutaneously, inhibited induced ovulation in immature rats treated with pregnant mare serum gonadotrophin (PMSG). A single injection was effective if given 52–55 h after the PMSG, i.e. in the 3 h period after the critical period before ovulation. The injection of serotonin inhibited the release of luteinizing hormone (LH) from the pituitary since the pituitary levels were higher than in the control animals and there was complete inhibition of the plasma LH surge. The antiovulatory effect was reversed by administration of progesterone and endogenous plasma progesterone levels were reduced in the late evening after serotonin treatment. The site of action of serotonin appeared to be peripheral since it inhibited induced ovulation in hypophysectomized rats but was without effect in intact rats treated intraventricularly. It is suggested that progesterone is essential for the occurrence of induced ovulation and serotonin inhibits either its secretion at the ovarian level or its passage away from the ovary.


1974 ◽  
Vol 52 (9) ◽  
pp. 744-750 ◽  
Author(s):  
W. H. Moger ◽  
D. T. Armstrong

Treatment of hypophysectomized immature male rats with luteinizing hormone (LH) greatly increased the metabolism of both 4-[14C]progesterone and 4-[14C]testosterone by testicular homogenates. Prolactin, either alone or in combination with LH, did not influence the metabolism of either substrate. Progesterone was metabolized to 17α-hydroxyprogesterone, androstenedione, 5α-pregnan-3,20-dione, 3α-hydroxy-5α-pregnan-20-one, and 3β-hydroxy-5α-pregnan-20-one. Testosterone was metabolized to dihydrotestosterone and 5α-androstan-3α,17β-diol. On the basis of these observations it is suggested that LH stimulated the 5α-reductase(s) of the immature rat testis. Testis homogenates from immature rats with intact pituitaries were incubated with 4-[14C]3α-hydroxy-5α-pregnan-20-one. Rapid conversion to androsterone was observed, with the formation of a compound chromatographically identical with 3α, 17α-dihydroxy-5α-pregnan-20-one as an apparent intermediate. These findings demonstrate the ability of the rat testes to form androsterone from progesterone by a pathway that does not involve testosterone.


1974 ◽  
Vol 52 (7) ◽  
pp. 586-593 ◽  
Author(s):  
Leo P. K. Lee

Advanced germinal cells (spermatocytes and spermatids) prepared from adult rat testes, but not other cells, released their cellular contents into the incubation medium when they were incubated at 37° at a physiological pH. Evidence was presented that the release of cellular contents was due to changes in the permeability of the plasma membranes of these cells. The hypothesis is advanced that the changes in the permeability of the plasma membranes of the advanced testicular germinal cells of the rat may be intimately associated with the cellular degeneration and cessation of spermatogenesis which occur in cryptorchid testes.


1975 ◽  
Vol 229 (4) ◽  
pp. 1102-1109 ◽  
Author(s):  
H Yamanaka ◽  
RY Kirdani ◽  
J Saroff ◽  
GP Murphy ◽  
AA Sandberg

Prostatic weights, 5alpha-reductase, and arginase activities were utilized as indexes for the effects of prolactin in short-term experiments in intact, hypophysectomized or castrated rats. Experiments were performed in which a dose-related response in the above parameters was obtained with testosterone administration in castrated mature and immature rats in order to evaluate the effects of simultaneously administered prolactin. This approach was necessitated by the failure of prolactin alone to affect the parameters listed in intact, castrated or hypophysectomized rats. It was shown that ovine prolactin may have an enhancing effect on the prostatic weight, 5alpha-reductase, and arginase activities, but that this effect is neither consistent nor striking when compared to that of testosterone.. Nevertheless, it is still possible that the long-term effects of prolactin, even if they are only of an enhancing quality, may play an important role in normal prostatic physiology and in abnormal states.


2020 ◽  
Vol 58 (1) ◽  
pp. 1199-1210
Author(s):  
Hongjie Wang ◽  
Boying Shan ◽  
Yulei Duan ◽  
Juan Zhu ◽  
Liping Jiang ◽  
...  

1974 ◽  
Vol 60 (2) ◽  
pp. 269-NP ◽  
Author(s):  
H. J. GALENA ◽  
C. TERNER

SUMMARY A method is described for the isolation of non-flagellate germinal cells of the testis. The interstitial cells were removed by submersion of teased seminiferous tubules in distilled water. The interstitial cells exposed to water burst while the germinal cells inside the tubules remained intact. The tubules were then homogenized in isotonic saline and the non-flagellate germinal cells (spermatocytes and young spermatids) were isolated by centrifugation and filtration through a layer of Sephadex G-25 gel. On incubation with progesterone these cells produced 17α-hydroxyprogesterone, androstenedione, and testosterone. The rate of conversion of progesterone to testosterone in vitro was 0·20 μg/h/109 germinal cells. These results suggest that the non-flagellate germinal cells of the testis may make a significant contribution to the production of androgens.


1978 ◽  
Vol 31 (1) ◽  
pp. 53 ◽  
Author(s):  
AW Blackshaw ◽  
PF Massey

Cryptorchidism of the mature rat testis led to degeneration of the seminiferous tubules and changes in enzyme patterns and activities. Spermatogenic stages 1--4, containing pachytene primary spermatocytes in late meiotic prophase, and stage 5, containing recently formed round spermatids, were damaged by 48 h. Within 96 h stages showed a loss of germinal cells into the lumen and this was almost complete by 192 h.


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