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Biomedical subjects

A R Chowdhury

Publications and source records attributed to A R Chowdhury.

At least 19 recordsLinked to original sources

Testicular toxicity of methylmercury: analysis of cellular distribution pattern at different stages of the seminiferous epithelium.

Stage-specific distribution of methylmercury (MM) and spermatogenic changes were analyzed in rats administered 5 or 10 micrograms MM/kg, ip, daily for 15, 30, 60, and 90 days. MM deposition, as grain number/cm2 was noted in basal portions at later stages on day 15, which increased gradually by day 90. MM deposition was in the order of stages IV, VII, XIV, IX, being higher in adluminal portions on days 30 and 60. MM-enriched cytoplasmic masses leaked out through disintegrated tubular membrane on days 60 and 90. Epithelial damage, at stages late XIV through IV, V through VI, VII through VIII, XIII through mid-XIV, and IX through XII, accorded with the gradual deposition of MM. As profound cell death occurred between zygotenes to pachytenes and dividing spermatocytes to step 1 spermatids, the spermatids were conspicuously decreased at later times. It is possible that MM distorts the barrier system at stages IX through XII, gets distributed within the tubule, and hence may pose a direct or Sertoli cell mediated effect at stages XII through early XIV in a dose-duration-MM burden related manner.

Animals

Steroidogenic inhibition in testicular tissue of formaldehyde exposed rats.

Three groups of rats (n = 10) were subjected to intraperitoneal treatment of formaldehyde daily at doses of 5, 10 and 15 mg/kg body weight over a period of 30 days. Gradual diminution in body and testicular weight was observed in all treated groups. Leyding cell impairement was conspicuous in those given doses of 10 and 15 mg/kg. Inhibition of 3 beta-delta 5-hydroxy steroid dehydrogenase and accumulation of sudanophillic materials in testicular tissue of formaldehyde treated rats was recorded histochemically. Significant decline of serum testosterone was also observed in the same groups. Structural and functional impairement of Leydig cells after formaldehyde treatment caused steroidogenic inhibition.

Animals

BHC induced testicular impairments in rats.

Benzene hexachloride (BHC) was fed to mature male rats weighing 160 g at dosages of 3 and 6 mg/kg body weight over a period of 180 days. Significant decrease in testicular weight and degeneration of seminiferous tubules with deformed spermatogenic cells were noted at a dose of 6 mg/kg BHC. Marked increase in BHC residue in testis revealed that the drug was able to cross blood-testis barrier.

Animals

Lindane induced changes in morphology and lipids profile of testes in rats.

Intraperitoneal treatment of adult male rats with lindane at dosages of 4 and 8 mg/kg over a period of 45 days caused retardation in body and testicular growth. Testicular degeneration was conspicuous over a period of 45 days in both dosages of lindane. After treatment with lindane, histochemical and biochemical studies revealed the accumulation of testicular lipid components, i.e. total lipids, triglycerides and cholesterol along with fatty degeneration in testicular tissues. Moreover, the loss of male accessory organ weight indicated androgen deficiency in treated rats.

Animals

Distribution of mercury and evaluation of testicular steroidogenesis in mercuric chloride and methylmercury administered rats.

Intraperitoneal administration of methylmercury chloride (MMC) and mercuric chloride (MC) to male rats in doses of 5, 10 micrograms MMC/kg or 50, 100 micrograms MC/kg for 90 days induced cellular disintegration of Leydig cells which was conspicuous on day 30 and onwards in the exposed groups. Progressive degeneration of Leydig cells and decrease in their nuclear diameter and population were associated with gradual increase in deposition of mercury. Gradual diminution of 3 beta-hydroxy-delta 5-steroid dehydrogenase activity in Leydig cells after MMC or MC treatment was correlated with different structural deformations of the cells over 90 days. Moreover, a significant decrease in serum testosterone levels by day 90 confirmed steroidogenic impairment after MMC or MC treatment.

3-Hydroxysteroid Dehydrogenases

Methylmercury- and mercuric-chloride-induced alterations in rat epididymal sperm.

Four-week-old male albino rats weighing 70 +/- 5 g were treated intraperitoneally daily with 0, 5 and 10 micrograms methylmercuric chloride (MMC)/kg or 0, 50 and 100 micrograms mercuric chloride (MC)/kg body weight, respectively, over a period of 90 days. Studies were carried out a intermittent intervals, i.e. on days 0, 15, 30, 60 and 90 of the experiment. Gradual decrements in body and epididymal weights were observed from day 30 onwards in both the MMC- and MC-treated groups. Morphological deformations of epididymal epithelium were noted from day 30 onwards in the mercurial-treated groups. MMC treatment caused severe degeneration of the epididymal epithelium on days 60 and 90 in comparison to MC treatment. Total sperm count was significantly less in the MC-treated groups, while motile sperm count was affected most in the MMC-administered groups. The frequency of sperm abnormality increased consistently at both doses of mercurial treatment over a period of 90 days. Maximum sperm abnormality among the treated groups was noted in the groups given 10 micrograms MMC/kg. The observations revealed that MMC and MC have variable potency to alter epididymal structure and the sperm.

Animals

Histological and pharmacological changes in vas deferens of rats exposed to hexachlorocyclohexane.

The effect of hexachlorocyclohexane (HCH) treatment in male albino rats at dosages of 3 and 6 mg/kg body weight by force-feeding were studied over a period of 180 days. Histological observations revealed graded degeneration in the muscular layer of vas deferens. Moreover, the accumulation of HCH residue in serum and vas deferens is highly significant in the experimental group. The contractility of muscles showed marked inhibition by in vitro study.

Administration, Oral

Trace elements in the endometrium of infertile women.

Some essential trace elements were estimated in endometrium of regularly menstruating fertile women and in women with infertility due to cervical factors. The distribution of the trace elements zinc, copper, iron, selenium and manganese at any particular phase of cycle remains more or less semilier between control (i.e. fertile) and infertile (primary and secondary) subjects.

Adult

Cytochemical alterations of adrenals in lead-treated rats.

Cytochemical investigations of steroid 3 beta-delta 5-OHD, sudanophilic substances, adenosine triphosphatase (ATPase), and adenosine monophosphatase (AMPase) activities in the adrenal of male young rats that had received lead acetate daily at dosages of 1 mg, 2 mg, 4 mg and 6 mg/kg intraperitoneally for 30 days revealed that lead treatment with low dosages (1 mg and 2 mg/kg) accelerated both cortical and medullary functions. Treatment with high dosages (4 mg and 6 mg/kg), however, inhibited the function of adrenals in both regions. Histochemical studies showed that the alteration in enzymatic activities in cortical and medullary regions revealed the possible mechanism of action of lead on the adrenals.

Adrenal Cortex

Testicular regulation and sub-cellular distribution of zinc in the epididymis and vas deferens of rhesus monkey (Macaca mulatta).

The zinc concentration in the epididymis (caput, corpus and cauda regions), vas deferens and caudal lobe of prostate of adult rhesus monkeys was determined by atomic absorption spectrophotometry. Zinc content (microgram/g wet weight) was found to be maximum in the prostate (709 micrograms) followed by epididymis and vas deferens. The three segments of the epididymis did not differ from one another in their zinc content (165-177 micrograms). On a protein basis maximum concentration of zinc was present in the nuclear fraction followed by microsomal, cytosolic and mitochondrial fractions in that order. Ligation of testicular efferent ducts or castration 90 days prior to autopsy caused a marked reduction in zinc concentration in different sub-cellular fractions of the organs examined; castration was relatively more effective in this regard. The importance of androgen and other testicular products in controlling zinc content and the possible physiological role of zinc in the male genital tract are discussed.

Animals

Histomorphometric and biochemical changes in the testicular tissues of rats treated with mercuric chloride.

Gradual alterations of testicular tissues were noted in rats treated with mercuric chloride at dosages of 0.05 mg/kg and 0.10 mg/kg body weight (i.p.) over a period of 90 days. Significant reduction in body and testicular weights were observed throughout the experimental period in treated animals. Consequently, testicular protein, DNA and RNA also exhibited a similar type of diminution in the same groups. Moreover, high cholesterol and low ascorbic acid concentrations were found in testis at both doses. Testicular degeneration and spermatogenic arrest were more pronounced in the high dose group over a period of 90 days.

Animals

Histochemical changes in the testes of lead induced experimental rats.

The experiments were performed on mature male rats divided in five groups, one control and four experimental in which the animals received 1 mg, 2 mg, 4 mg and 6 mg/kg body weight lead acetate intraperitoneally respectively, over a period of 30 days. ALA-D and lead was estimated in the blood by the use of atomic absorption spectrophotometer and ATP-ase, AMP-ase, Alk-ase were histochemically localized. Significant increase in blood and testis of lead levels along with decrease of ALA-D levels were observed. Changes in the testicular tissue were encountered. Other details concerned with the damage of the testicular tissue are discussed.

Adenosine Triphosphatases