Search PubMed⌕ Search

Biomedical subjects

C J Dominic

Publications and source records attributed to C J Dominic.

At least 37 records · Page 2Linked to original sources

The male-induced pregnancy block (the Bruce effect) in mice: re-evaluation of the ability of exogenous progesterone in preventing implantation failure.

The ability of exogenous progesterone administration to prevent implantation failure in newly inseminated females exposed to alien males for 3 days (from 10.00 hr on day 1 to 10.00 hr on day 4 post coitum) was evaluated. Administration of progesterone, 1 mg/female/day, for 5 days beginning at 10.00 hr on day 1 or at 10.00 hr on day 2 prevented the return of oestrus and induced implantation of blastocysts in alien male-exposed females. Administration of progesterone beginning at 22.00 hr on day 2 was only partially effective in preventing return of oestrus in the male-exposed females; however, the majority of the females which exhibited vaginal oestrus showed implanted embryos. Progesterone injection beginning at 10.00 hr on day 3 or later was totally ineffective in preventing return of oestrus in the females. Administration of progesterone beginning at 10.00 hr or at 22.00 hr on day 3 failed to induce implantation in the male-exposed females which returned to oestrus on day 3; however, the treatment induced implantation in the majority of the females which returned to oestrus on day 4. Progesterone administration beginning at 10.00 hr on day 4 was totally ineffective in inducing implantation in the male-exposed females exhibiting the Bruce effect. The results indicate that administration of progesterone beginning at any time prior to the appearance of oestrus facilitates implantation of blastocysts in male-exposed females; however, progesterone administration beginning after the onset of oestrus is totally ineffective in inducing implantation in females. The results also strongly suggest that in females exhibiting the Bruce effect there is a total loss of the blastocysts.

Animals↗

Effect of bilateral transection of the lateral olfactory tract on the male-induced implantation failure (the Bruce effect) in mice.

Bilateral transection of the lateral olfactory tract (LOT) at the rostral level induced anosmia in female mice; by contrast, sectioning of the LOT at more caudal levels failed to induce anosmia in females. Transection of the LOT at all the levels inhibited the alien male-induced implantation failure in newly inseminated mice (the Bruce effect). Sham-operated as well as intact females exhibited a high rate of implantation failure following alien male exposure. The results suggest that the inhibition of the Bruce effect in LOT-transected females is not due to anosmia induced by the operation procedure, but due to interruption of the primary olfactory bulb projections to the posterior parts of the olfactory cortex. Our results rule out the involvement of the nervus terminalis in the Bruce effect. The present report lends support to the involvement of the accessory olfactory system in the transmission of the pheromonal stimulus involved in the male-induced implantation failure.

Animals↗

Prostaglandin F2 alpha-induced changes in the sex organs of the male laboratory mouse.

Administration (3 mg/kg body weight/day, for 21 days) of prostaglandin F2 alpha (PGF2 alpha) caused marked suppression of spermatogenesis and significant reduction in the weights of the testis, epididymis and accessory sex glands. The seminiferous tubules were devoid of spermatozoa and contained only Sertoli cells, spermatogonia, spermatocytes and occasionally spermatids; several multinucleated giant cells were observed in the lumen of the tubules. The Leydig cells were atrophied. The levels of RNA, DNA and protein in the testis were, however, unaffected by drug therapy. In drug-treated mice the epididymal epithelium presented a degenerate appearance; the lumen was generally devoid of spermatozoa and contained mainly exfoliated immature germ cells and sperm debris; cauda epididymidal spermatozoa, when present, were immotile and fragmented. PGF2 alpha treatment also caused significant decrease in the levels of sialic acid in the caput and cauda epididymides and of fructose in the seminal vesicle. The results suggest that the regressive changes induced by PGF2 alpha in the reproductive organs of the mouse are due to the interference with the secretion of androgen. The alterations induced in the reproductive organs by administration of PGF2 alpha were reversible and 56 days after drug withdrawal the organs returned to their normal state.

Animals↗

Effect of 1-p-chlorobenzyl-1H-indazol-3-carboxylic acid (AF 1312/Ts) on the sex organs of the male laboratory mouse.

Oral administration (500 mg/kg body weight/day, for 28 days) of 1-p-chlorobenzyl-1H-indazol-3-carboxylic acid (AF 1312/TS) induced suppression of spermatogenesis without adversely affecting the Leydig cells. The seminiferous tubules were almost depopulated and contained only Sertoli cells and spermatogonia. The drug also induced significant decrease in the levels of testicular RNA and protein; DNA level, however, remained unaltered. Regressive histological changes were also noted in the epididymides of drug-treated mice. Cauda epididymidal spermatozoa from drug-treated mice were immotile and fragmented. AF 1312/TS caused no alteration in the level of fructose in the seminal vesicle. The drug-induced alterations were reversible, and 56 days after drug withdrawal the reproductive organs returned to their pretreatment state. The results suggest that AF 1312/TS selectively suppresses spermatogenesis without interfering with the endocrine functions of the testis.

Animals↗

Influence of conspecific males on the oestrous cycle of underfed female mice.

Female mice maintained on restricted diet (3.5, 3.0 and 2.5 gm/female/day) exhibited disturbances in the oestrous cycle which were directly related to the degree of diet restriction. Females maintained on restricted diet, 2.5 gm/day, showed complete suppression of the oestrous cycle. The presence of a conspecific male was effective in maintaining normal oestrous cycles in underfed females to some extent. It is suggested that the ability of males to maintain oestrous cycle in underfed females is due to the stimulatory influence of the male-originating pheromone on hypophysial gonadotrophin secretion.

Animals↗

Effect of 1-(2, 4-dichlorobenzyl)-1H-indazole-3-carboxylic acid (DICA) on the sex organs of the male laboratory mouse.

Oral administration (50 mg/kg body weight/day, for 28 days) of 1-(2,4-dichlorobenzyl)-1H-indazole-3-carboxylic acid (DICA) induced significant reduction in testicular weight with suppression of spermatogenesis. The seminiferous tubules were devoid of spermatozoa and contained only Sertoli cells, spermatogonia, spermatocytes and several multinucleated giant cells. The Leydig cells, however, remained unaffected in treated animals. The drug also induced significant decrease in the levels of testicular RNA and protein; DNA level, however, remained unaltered. Epididymis in DICA-treated mice presented normal histology except that the lumen contained sperm debris; cauda epididymidal spermatozoa were immotile and often fragmented. DICA treatment caused no change in the level of fructose in the seminal vesicle. DICA-induced alterations were reversible and within 56 days of drug withdrawal the reproductive organs returned to their normal state.

Animals↗

Evaluation of the involvement of the adrenals in the pheromonal influences on the oestrous cycle of laboratory mice.

Unisexual grouping of female mice induced irregularities in their oestrous cycles. However, no significant difference in body weight and in the weights of adrenals, uteri and ovaries and in the adrenal delta 5 3 beta-hydroxysteroid dehydrogenase (HSD) activity was found between unisexually grouped females and individually housed females. Adrenalectomy of females failed to prevent the oestrous cycle irregularities induced by unisexual grouping. Furthermore, adrenalectomized females in unisexual groups responded to exposure to males by exhibiting oestrus acceleration and synchronization (the Whitten effect). The results rule out the involvement of the adrenals in the oestrous cycle irregularities induced by unisexual grouping and in the induction of the Whitten effect in unisexually grouped females.

3-Hydroxysteroid Dehydrogenases↗

Studies of the male-originating pheromones involved in the Whitten effect and Bruce effect in mice.

Experiments were designed to elucidate the mode of transmission of the male-originating pheromones involved in the induction of estrus (the Whitten effect) and in implantation failure (the Bruce effect) in mice. The Whitten effect was induced in unisexually grouped females by exposure to corralled males, and also by corralled males housed within a perforated cage (which prevented physical contact of the females with the male-originating pheromone). The results suggest that the pheromone involved in the Whitten effect is volatile (airborne). Implantation failure occurred in a significantly high proportion of newly inseminated females when they were individually confined in corrals and housed below corralled alien males. By contrast, implantation failure was significantly reduced when corralled females were housed above corralled alien males. The results indicate that the male-originating pheromone involved in the Bruce effect is nonvolatile and acts on the females through contact. It is suggested that the pheromone involved in the Whitten effect is distinct from the one involved in the Bruce effect.

Animals↗