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1.
Indian J Physiol Pharmacol ; 2008 Jul-Sept; 52(3): 274-282
Article in English | IMSEAR | ID: sea-145878

ABSTRACT

Objective : To evaluate various causes possibly contributing towards recurrent pregnancy loss (RPL), particularly male factors. Prospective study of 75 couples with history of RPL who were investigated for genetic, anatomic, immunological, infective and systemic causes in both partners. Functional sperm capacity was assessed by the Hypo-osmotic swelling test (HOS), Acrosomal Reaction (AR), Nuclear condensationdecondensation test (NCD) and Seminal Total Leukocyte Count (TLC) along with semen analysis. Twenty male volunteers with recently proven fertility were also included for detailed sperm morphology and sperm functions test as controls. Amongst male partners 3(4%) had varicocele, 23(30.6%) had infection, 1(1.3%) immunological and 1(1.3%) had genetic abnormality. Sperm motility, viability and sperm function tests were significantly lower in the RPL group as compared to the control group (P=0.000). Male factor might be a possible contributing factor towards RPL. Both the partners should be evaluated and treated simultaneously in order to achieve desirable outcome.

2.
Indian J Physiol Pharmacol ; 2008 Jul-Sept; 52(3): 267-273
Article in English | IMSEAR | ID: sea-145877

ABSTRACT

Release of copper and its effect on functional integrity of human sperms in vitro were assessed following co-incubation of semen with CuT 380A. After 30 min of incubation with semen, release of copper ions from CuT 380A was found to be 9.2 to 40 times higher compared to control incubations with PBS. Sperm function tests, when simultaneously performed following loss of motility in sperms (>95%) after 120 min of copper exposure, depicted a significant (P<0.001) reduction in sperm viability and hypo-osmotic swelling (HOS) response. However, the affected sperm populations revealed no significant alterations in other functional tests like acrosomal status or nuclear chromatin decondensation. It is therefore concluded that the high release of copper from CuT 380A drastically lowers sperm motility. viability and HOS response but only marginally affects the acrosome status or nuclear chromatin condensation in short term incubations.

3.
Indian J Exp Biol ; 2005 Nov; 43(11): 1080-7
Article in English | IMSEAR | ID: sea-57076

ABSTRACT

Germ cell death and their removal from the seminiferous epithelium are common in the affected testis in conditions of unilateral ischemia or cryptorchidism; the similarities and differences, however, have not been studied between these two conditions. The present study was designed to examine the severity of the effect on testicular germ cells during the initial stages of both ischemia and cryptorchidism, which have significant implications on the restoration of fertility following surgical repair. Complete absence of spermatids was observed following 12 hr of ischemia as compared to 7 days of cryptorchidism. Germ cell removal in either case was in the direction of lumen to basement membrane leaving only a single layer of cells by 24 hr of unilateral ischemia as compared to 15 days of cryptorchidism. Levels of intratesticular testosterone was found lower in cryptorchidism (7 days) but not in ischemia till 24 hrs. Giant cells frequently observed in cryptorchid testis were absent in the ischemic seminiferous epithelium. There was a gradual increase in the number of apoptotic and non-viable cells; the latter was more than 95% by 24 hr of ischemia. In contrast, approximately 85% testicular cells were nonviable till 15 days of cryptorchidism. The 1c peak representing the population of haploid cells was significantly reduced in cryptorchidism (7 days), while the peak was completely abolished by 24 hr of ischemia. Rise in the levels of oxidative stress in the affected testis was observed identically during the initial stages. These findings indicate that coupled with the rise in tissue oxidative stress, the number of apoptotic/nonviable germ cells was alarmingly high (> 80%) by 15 days of cryptochidism or 24 hr of ischemia. Restoration of complete spermatogenesis following surgical repair may not be possible in such cases because of these acute adverse effects.


Subject(s)
Animals , Apoptosis , Cell Survival , Cryptorchidism/pathology , DNA/chemistry , Flow Cytometry , Germ Cells/pathology , Haploidy , Hormones/metabolism , In Situ Nick-End Labeling , Ischemia/pathology , Lipid Peroxidation , Male , Oxidative Stress , Rats , Seminiferous Epithelium/pathology , Testicular Diseases/pathology , Testis/pathology , Testosterone/pharmacology , Time Factors
4.
Indian J Pediatr ; 1999 Mar-Apr; 66(2): 193-6
Article in English | IMSEAR | ID: sea-82870

ABSTRACT

It is a common clinical practice to estimate FSH, LH and testosterone levels in patients with unilateral undescended testis (U/L UDT) as a prognostic pointer to fertility potential. Is this practice correct? To ascertain this aspect, new born rats were operated to create experimental U/L UDT by gubernaculectomy and anchoring the gubernaculum to anterior abdominal wall. Fertility and hormone levels were evaluated later in adult life. Though fertility of rats with U/L UDT was significantly less (p < 0.01) than the controls, no significant alterations were found in the levels of serum testosterone, FSH and LH. Even though variations in the hormone levels may be responsible, to a certain extent, for the decrease in fertility potential in U/L UDT, estimation of sex hormone levels in U/L UDT is not a sensitive indicator of fertility potential. U/L UDT may additionally be affecting fertility through non-endocrinological mechanisms.


Subject(s)
Animals , Cryptorchidism/blood , Fertility , Follicle Stimulating Hormone/blood , Luteinizing Hormone/blood , Male , Prognosis , Rats , Rats, Wistar , Testosterone/blood
5.
Indian J Exp Biol ; 1997 Jun; 35(6): 576-80
Article in English | IMSEAR | ID: sea-60602

ABSTRACT

Vitamin A in graded doses of 125, 250 and 375 U.S.P./kg body wt, po, for 10 days (d 21-30) drastically reduced the testicular weight by 25 to 62% and seminiferous tubular diameter by 14 to 35% in prepubertal rats in lowest and highest doses of the treatment. The treatment induced disproportionate enlargement of nuclei and cytoplasm of the germ cells; predominantly the preleptotene and pachytene spermatocytes. These abnormal germ cells, often with 2 or 3 nuclei displayed vacuolated cytoplasm surrounding pyknotic or granulated or dispersed chromatin granules within the nuclei in a dose proportionate manner. The round spermatids were the most sensitive cell types which completely disappeared in two higher doses of treatment. Vacuolation of Sertoli cell cytoplasm in about 25% of the tubules with associated increase in intertubular space was also observed in rats treated with the highest dose of the vitamin. Circulatory levels of FSH, LH and testosterone remained unaltered following the vitamin excess treatment. Therefore, it is suggested that excess vitamin A even for shorter duration like the present one is detrimental to developing cell types and prevents the progress of the spermatogenic process beyond the round spermatid stage.


Subject(s)
Animals , Cellular Senescence/drug effects , Germ Cells/drug effects , Hypervitaminosis A/pathology , Male , Rats , Sexual Maturation , Testis/drug effects
6.
Indian J Exp Biol ; 1992 Jul; 30(7): 567-73
Article in English | IMSEAR | ID: sea-58554

ABSTRACT

Adult rats treated with a GnRH antagonist (Ac D2Nal1, D4Cl Phe2, DTrp3, DArg6, DAla10 GnRH; code: 103-289-10, National Institutes of Health, USA) for 5 weeks (250 micrograms/kg b.w) showed multiple degrees of impairment and atrophy of the genital organs concomitant with decreased serum levels of testosterone, LH and FSH. Inhibition of spermatogenesis was characterized by germ cell degeneration and overall decline in different cell numbers and in particular, spermatids of any kind were completely absent. Testosterone supplementation (60 micrograms/rat/day, sc) to GnRH antagonist treated rats, for the same period, significantly elevated the weights of the sex organs, and the serum levels of hormones. Spermatogenesis was improved both qualitatively and quantitatively; albeit failed to be restored back to control levels. Treatment with estradiol 17 beta (1 microgram/rat/day) for 5 weeks had insignificant effect on spermatogenesis but the weights of the genital organs (seminal vesicles by 19% and ventral prostate by 40%) and the levels of serum hormones (LH by 24%, FSH 22% and testosterone by 25%) were otherwise reduced. Administration of testosterone either alone or in combination with estradiol 17 beta had only a marginal effect on spermatogenesis or on other reproductive parameters. The results indicate a positive shift in the response of the testis and serum levels of gonadotropins to testosterone supplementation in rats treated with either GnRH antagonist or estradiol 17 beta.


Subject(s)
Animals , Estradiol/pharmacology , Gonadotropin-Releasing Hormone/antagonists & inhibitors , Gonadotropins/blood , Male , Rats , Spermatogenesis/drug effects , Testis/drug effects , Testosterone/pharmacology
7.
Indian J Exp Biol ; 1990 Jan; 28(1): 27-31
Article in English | IMSEAR | ID: sea-59095

ABSTRACT

Atypical flagellar structures containing eight subfibers arrayed around a single, central element (8 + 1) are associated with pituitary secretory cells, largely gonadotropes. Less frequently, flagella with a 7 + 2 pattern are seen. Both types appear commonly in pituitary tissues obtained from both male and female rats above 1 year of age and appear to penetrate the cells. Except for the pattern of the array, the structures are similar in dimension to commonly observed flagellar structures (9 + 2) when viewed in sections cut either in perpendicular or sagittal to the major axis. The (8 + 1) flagella are observed both singly and in pairs. Steroidal milieu (ovariectomy with or without steroid replacement) does not seem to influence their appearance. Flagella with the common 9 + 2 arrangement are not observed in the rat pituitary.


Subject(s)
Animals , Female , Flagella/ultrastructure , Male , Microscopy, Electron , Ovariectomy , Pituitary Gland/ultrastructure , Rats , Rats, Inbred Strains
8.
Indian J Physiol Pharmacol ; 1986 Apr-Jun; 30(2): 161-5
Article in English | IMSEAR | ID: sea-108976

ABSTRACT

A single intra-uterine injection of 60 microliters of dimethylsulfoxide prevented implantation when administered before mating and induced resorption of the conceptus in rats when given during early pregnancy.


Subject(s)
Animals , Dimethyl Sulfoxide/administration & dosage , Embryo Implantation/drug effects , Fallopian Tubes , Female , Fetal Death/chemically induced , Injections , Pregnancy , Rats
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