Thermal stress causes oxidative stress and physiological changes in female rabbits.

The present study investigated the effects of heat stress on oxidative stress status and physiological changes using female New Zealand White rabbits. 24 sexually mature female rabbits weighing 1953.1-2375.4 g were divided into 4 groups of 6 animals each and subjected to ambient temperature (T0: 19-26 °C), 27-28 °C for T1, 31-32 °C for T2 and 35-36 °C for T3 using electrical heaters from 8:00 a.m. to 4:00 p.m. daily for 30 days. Feed intake and body weight gain were recorded daily. Behavioral alterations of anxiety, dizziness, aggression, withdrawal, impaired feed intake were observed. At the end of experimental period animals were sacrificed, blood samples and vital organs such as liver, kidney, heart, ovaries, uterus collected for appropriate analysis. Results revealed that animals of T2 and T3 had an 11% decrease in the final body weights and 62% body weight gain but increase in feed conversion ratio by 64.81%, 24.19% water intake, 3.64% in rectal and 2.42% in skin temperature compared to the control. Dizziness, withdrawal to a corner of the cage and reduced feed intake were observed. The live weight of lungs and kidneys increased by 37.71% and 33.78% while that of ovaries and uterus decreased in the same animals of T2 and T3. Animals from T2 and T3 showed significant decrease (p < 0.05) by 23.64% in hemoglobin concentration, 12.73% in red blood cells, 11.93% in packed cell volume, 12.02% in total protein while mean corpuscular volume, white blood cells, lymphocytes, creatinine, urea and aspartate transaminase increased respectively by 10.73%, 42.37%, 15.53%, 28.98%, 53.2% and 23.31% compared to the control. The kidney level of malondialdehyde was significantly increased in T2 and T3 animals by 74.29%, whereas protein, catalase, superoxide dismutase and glutathione peroxidase activity were significantly lower (p < 0.05) compared with control. It was concluded that long-term exposure of female rabbits to elevated ambient temperatures induces heat stress and accompanying oxidative stress that consequently impairs physiological function.

The pesticide heptachlor affects steroid hormone secretion in isolated follicular and luteal cells of rat.

Heptachlor, a chlorinated hydrocarbon pesticide, suppresses the production of progesterone and estradiol in the female rat in vivo or in isolated ovaries in vitro. In this study the effect of heptachlor on steroid hormone production by isolated rat luteal and follicular cells, in the presence of two precursor hormones was investigated. Ovaries were isolated from anesthetized mature normocyclic virgin rats (3 to 4 months old), under sterile conditions. Corpora lutea and follicles were microscopically dissected out and separately enzymatically dispersed with collagenase at 37 degrees C. Viable cells collected after centrifugation were used at a concentration of approximately 2.5 x 10(5) cells/10 mL. Both luteal and follicular cell preparations were separately incubated overnight (15 h) at 37 degrees C in the presence of pregnenolone (P5) and androstenedione (A4) at a concentration of 6.0 nmol/L each, and heptachlor at either 0.12 microg/mL (low dose) or 1.20 microg/mL (high dose) (test cells) or in the absence of heptachlor (control cells). At the end of the incubations, progesterone and estradiol 17beta levels were analyzed in the incubation media. The results indicate that heptachlor significantly suppressed the production of both progesterone and estradiol in both cell types in a dose related manner even in the presence of A4 and P5 as precursor hormones (P<0.05).

In vivo and in vitro effects of graded doses of the pesticide heptachlor on female sex steroid hormone production in rats.

Adult female Sprague-Dawley rats were injected with corn oil or 5 mg, 20 mg, 25 mg or 30 mg per kg body weight of heptachlor solution every other day for up to 18 days. The rats were killed at the end of the experimental period, and blood samples were assayed for progesterone and oestrogen by radioimmunoassay. Ovarian cells from the rats were isolated and incubated either on their own, or in the presence of LH or FSH, and production of progesterone and oestrogen determined. Control incubations consisted of cells from corn oil-treated rats. The latter were also incubated on their own or in the presence of LH or FSH. Heptachlor significantly suppressed blood progesterone and oestradiol levels (P < 0.05 to P < 0.001), the degree of suppression depending on the dose and the stage of the oestrous cycle in which samples were obtained. Production of oestradiol by ovarian cells from heptachlor-treated rats was lower than for corn oil-treated controls. Cells from rats treated with low doses of heptachlor (5 mg per kg body weight) showed an increased production of progesterone, while high doses (> 20 mg per kg body weight) suppressed production.

Effects of graded doses of the pesticide heptachlor on body weight, mating success, oestrous cycle, gestation length and litter size in laboratory rats.

Adult female Sprague-Dawley rats were injected with 5 or 20 mg/kg body weight heptachlor solution every other day for up to 18 days. They were weighed every day and the stage of oestrus determined by vaginal smears. One experimental group was mated and pregnancy characteristics studied. Heptachlor affected body weights, cycle patterns, length of gestation period and litter sizes in a dose-related manner. At a dose of 20 mg/kg body weight, heptachlor caused a significant decrease in average body weight (P < 0.01), disrupted and/or prolonged oestrous cycles, decreased mating success (P < 0.001), slightly increased gestation length (P < 0.05) and decreased litter size (P < 0.01).

Effects of 6-hydroxydopamine on testosterone production by mouse leydig cells in vitro.

Increasing doses (15 to 1000 micrograms/ml) of 6-hydroxydopamine (6-OHDA) stimulated, then suppressed testosterone production by mouse leydig cells incubated for 3 h in vitro. The stimulating doses ranged between 50 and 100 micrograms/ml, with maximal effects occurring at 30 to 60 minutes after the start of the treatments. At doses of 500 micrograms/ml, 6-OHDA exhibited inhibitory effects. When added to leydig cell incubations together with stimulating doses of luteinising hormone (LH), 1-(3',4'-dihydroxyphenil)2-isopropylaminoethanol (L-isoproterenol) or 8-bromoadenosine 3':5'-cyclic monophosphate (8-Br-cAMP), 6-OHDA abolished the effects of the latter compounds. Prolactin and prostaglandin E2 (PGE2) inhibited the stimulating effects of 8-Br-cAMP but not LH. It is proposed that the actions of 8-OHDA affect intracellular sites yet to be identified, thereby inhibiting testosterone production by mouse Leydig cells. Some of the actions of 6-OHDA seem to be medicated via beta-adrenergic receptors as the latter abolishes the stimulatory effects of L-isoproterenol, a potent beta-adrenergic agonist. However, the inability of stimulatory doses of LH and 8-Br-cAMP to reverse the inhibitory effects of 6-OHDA point to the possibility that other actions of 6-OHDA may be relayed via a second messenger system separate from that involving cAMP.

Partial purification of a putative membrane bound androgen binding protein in the dog cauda epididymis.

1. An androgen binding protein(s) has been partially purified from cell plasma membranes of dog epididymides. 2. The protein(s) has a pI of 5.3 and an association constant of (1.13 x 10(9) M-1). 3. Conclusive demonstration of androgen receptors in epididymal plasma membranes would be of significance in understanding epididymal physiology.

Regional and geographical variations in infertility: effects of environmental, cultural, and socioeconomic factors.

Fertility is affected by many different cultural, environmental, and socioeconomic factors, especially in developing countries where poverty and infections are commonplace. Environmental factors play a major role in infertility in Africa. One of the most important health problems in sub-Saharan Africa is the high rate of infertility and childlessness. The African society has a strong traditional heritage, and the study of the patterns of infertility in this part of the world would be incomplete without consideration of the sociocultural and environmental factors. The most cost-effective approach to solving the infertility problems in Africa is prevention and education. In Mexico, problems of reproductive health are associated with pregnancy in adolescents, sexually transmitted diseases and genitourinary neoplasms. Infertility affects 10% of couples, usually as a result of asymptomatic infection. Education, poverty, nutrition, and pollution are problems that must be tackled. The government has taken positive action in the State of São Paulo in Brazil, where gender discrimination is a major factor affecting women's health and reproductive outcomes. The implementation of new policies with adequate funding has resulted in marked improvements.

PIP: The impact of cultural, environmental, and socioeconomic factors on reproductive health and infertility are discussed in general terms. Conditions in sub-Saharan Africa, Kenya, Mexico, and Brazil are described. In Mexico, high levels of arsenic in drinking water pose a major environmental hazard affecting reproductive health. Chronic arsenic poisoning in Comarca Lagunera, Mexico, contributes to male infertility and birth defects. Additional problems are adolescent pregnancy, sexually transmitted diseases (STDs), congenital malformations, genitourinary neoplasms, malnourishment, and poverty. The example of Sao Paolo's investment in the well-being of women shows how effective government policy can accomplish rapid improvement in women's health. Infertility in Africa is around 30-40%. Infertility in the US is only 8%. The African cultural emphasis on women's status and childbearing makes infertility a major concern. African infertility is related to disease. In the Cameroon, over 50% of infertility is accounted for by pelvic inflammatory disease. Prevention programs should include improvement in diagnosis and treatment of sexually transmitted diseases (STDs), sex education for men and women, expanded family planning (FP) services, and better obstetric care. Infertility in Zaire, Cameroon, Gabon, and Uganda is high compared to other non-African countries. Infertility is geographically and ethnically variable within each country. Politics and government FP policy, traditional attitudes, polygamous relationships, and induced abortion all impact on infertility. Traditional practices, such as female genital mutilation, result in infections during the healing process; infections also occur during childbirth. Vesico-vaginal fistula and incontinence are problematic and can be corrected through surgical methods. Illegal abortions contribute to morbidity and mortality. STDs are a main cause of infertility in Kenya. Cultural beliefs place the blame on females. In both Africa and Mexico, men account for 30% of couple infertility.