The Absence of Pineal Melatonin Abolishes the Daily Rhythm of Tph1 (Tryptophan Hydroxylase 1), Asmt (Acetylserotonin O-Methyltransferase), and Aanat (Aralkylamine N-Acetyltransferase) mRNA Expressions in Rat Testes.

This study examined the effects of pinealectomy in Wistar rats and melatonin replacement therapy on the daily mRNA expression of melatonin (Tph1, Aanat, Asmt, Mt1, Mt2, and Rorα), and steroidogenic (Star, 17ßhsd3, and Lhr) related genes as well as clock genes (Rev-erbα, Bmal1, Per1, Per2, Cry1, and Cry2) in testes. The testes of control animals express the Tph1, Aanat, and Asmt and Per2 genes with 24-h rhythms in mRNA, reaching the maximal values during the dark phase. Pinealectomy abolished and melatonin treatment restored the 24-h rhythmicity. Daytime differences in mRNA expression were significant for Star, Lhr, Mt1, Mt2, Rorα, Rev-erbα, Bmal1, Cry1, and Cry2 genes in testes of control rats. Conversely, 17ßhsd3 and Per1 mRNA expression did not show a daytime difference in testes of control animals. Pinealectomy abolished the peak time of Mt1 and Mt2 mRNA expression, phase shifted the peak time of Star, Rorα, Rev-erbα, Bmal1, and Cry2 mRNA expression, downregulated the 24-h Lhr mRNA expression, and inverted the peak time of Per1, Per2, and Cry1 mRNA expression to the light phase. The melatonin replacement therapy completely restored the control levels of Lhr, Rev-erbα, and Per1 mRNA expression patterns, partially restored the daily control of Star, Mt2, Rorα, Bmal1, Cry1, and Cry2 mRNA expression but did not re-establish the daily control of Mt1 mRNA expression. This suggests that the daily mRNA expression of these genes is probably driven by pineal melatonin and melatonin treatment restores (partially or completely) the daily control of gene expression patterns.

Daily differential expression of melatonin-related genes and clock genes in rat cumulus-oocyte complex: changes after pinealectomy.

This study investigated the maturational stage (immature and mature ovaries) differences of mRNA expression of melatonin-forming enzymes (Aanat and Asmt), melatonin membrane receptors (Mt1 and Mt2) and putative nuclear (Rorα) receptors, and clock genes (Clock, Bmal1, Per1, Per2, Cry1, Cry2) in cumulus-oocyte complexes (COC) from weaning Wistar rats. We also examined the effects of pinealectomy and of melatonin pharmacological replacement on the daily expression of these genes in COC. qRT-PCR analysis revealed that in oocytes, the mRNA expression of Asmt, Mt2, Clock, Bmal1, Per2, and Cry1 were higher (P < 0.05) in immature ovaries than in the mature ones. In cumulus cells, the same pattern of mRNA expression for Asmt, Aanat, Rorα, Clock, Per1, Cry1, and Cry2 genes was observed. In oocytes, pinealectomy altered the daily mRNA expression profiles of Asmt, Mt1, Mt2, Clock, Per1, Cry1, and Cry2 genes. In cumulus cells, removal of the pineal altered the mRNA expression profiles of Mt1, Mt2, Rorα, Aanat, Asmt, Clock, Bmal1, Per2, Cry1, and Cry2 genes. Melatonin treatment partially or completely re-established the daily mRNA expression profiles of most genes studied. The mRNA expression of melatonin-related genes and clock genes in rat COC varies with the maturational stage of the meiotic cellular cycle in addition to the hour of the day. This suggests that melatonin might act differentially in accordance with the maturational stage of cumulus/oocyte complex. In addition, it seems that circulating pineal melatonin is very important in the design of the daily profile of mRNA expression of COC clock genes and genes related to melatonin synthesis and action.

Effect of melatonin on DNA damage of bovine cumulus cells during in vitro maturation (IVM) and on in vitro embryo development.

The effect of melatonin during in vitro maturation (IVM) on DNA damage of cumulus cells (CCs) from bovine cumulus-oocyte complexes (COCs) and embryo development was evaluated. COCs from abattoir ovaries were cultured in maturation medium (MM) with 0.5µg/ml FSH and 5.0µg/ml LH (FSH-LH); 10(-9)M melatonin (MEL) or FSH-LH+MEL (FSH-LH-MEL). After 24h of in vitro maturation, the CCs surrounding the oocyte were subjected to DNA analysis by Comet assay. After in vitro fertilization and in vitro embryo culture, the embryo development rates were evaluated on day 2 post insemination (cleavage) and days 7-8 (blastocyst). The percentage of CCs with no DNA damage was significantly superior in MEL group (37.6±2.4) than in FSH-LH-MEL (28.0±2.4) and FSH-LH (17.8±2.41) groups. Cleavage and blastocysts rates were similar among groups. Melatonin during IVM protects the CCs from DNA damage but this effect did not influence embryo development in vitro.

Progesterona plasmática de ovelhas submetidas ao efeito-macho e mantidas sob diferentes condições nutricionais / Plasmatic progesterone of ewes submitted to male effect and kept at different nutritional conditions

Dosou-se a concentração plasmática de progesterona (P4) em ovelhas Santa Inês (SI), Suffolk (SU) e Romney Marsh (RM) em anestro sazonal e submetidas ao efeito-macho, as quais receberam ou não suplementação alimentar. Machos vasectomizados foram introduzidos no grupo de fêmeas após um período prévio de isolamento de 60 dias, e amostras de sangue foram colhidas antes e após a introdução dos machos. Houve efeito (P<0,01) de período, raça, interação período x raça e interação suplementação x período x raça sobre a concentração de P4. Nas ovelhas SI ocorreu aumento (P<0,01) da concentração de P4 após a introdução do macho, indicando que houve aumento na atividade cíclica reprodutiva desse grupo. A suplementação, neste caso, potencializou este aumento. Nas ovelhas SU e RM não ocorreram modificações na concentração de P4 (P>0,01) após a introdução dos machos, nem houve efeito de suplementação. O efeito-macho foi eficaz em induzir a atividade reprodutiva durante o anestro sazonal em ovelhas SI, mas não em ovelhas SU e RM, e a associação dessa prática com a suplementação alimentar é recomendada para ovelhas da raça nativa SI.

The present study aimed to verify the plasmatic progesterone (P4) concentrations in Santa Inês (SI), Suffolk (SU) and Romney Marsh (RM) ewes submitted to male effect receiving or not food supplementation during seasonal anestrous. Vasectomized rams were introduced to the group of ewes after 60 day isolation. Blood samples were collected before and after the male's introduction. Effects (P<0.01) of period, breed, period x breed interaction and period x breed x supplementation interaction on plasmatic P 4 concentrations were observed. The plasmatic P 4 concentrations of SI ewes increased (P<0.01) after the male introduction, indicating there was an increase in the reproductive activity in this group. Supplementation increased this effect. For SU and RM ewes the plasmatic P 4 concentrations did not alter (P>0.01) after the male introduction, with no supplementation. It was concluded the male effect was efficient in inducing the reproductive activity in SI ewes, but not in SU and RM ewes. The association of the effect of the male with supplementation increased this effect.

Concentrações plasmáticas de testosterona, triiodotironina (T3) e tiroxina (T4) em bodes submetidos ao estresse calórico / Plasma concentrations of testosterone, triiodothyronine (T3), and thyroxine (T4) in bucks submitted to heat stress

Para verificar o efeito do estresse calórico (EC) nas concentrações plasmáticas de testosterona, triiodotironina (T3) e tiroxina (T4), oito bodes, das raças Saanen (n=4) e Alpina (n=4), foram mantidos em câmara bioclimática, sob condições de termoneutralidade (13,0ºC a 26,7ºC) durante 30 dias e, após um período (60 dias) de descanso, submetidos ao EC (23,7ºC a 34,0ºC) por 30 dias. Para minimizar as variações sazonais nos perfis hormonais devido ao fotoperíodo, durante toda fase experimental, incluindo a de adaptação em condições de termoneutralidade (30 dias), o fotoperíodo foi controlado utilizando-se alternância de dias longos (16h de luz e 8h de escuro) e de dias curtos (8h de luz e 16h de escuro) a cada 30 dias. As amostras de sangue foram coletadas duas vezes por semana durante cinco semanas. No conjunto das raças, o EC não influenciou (P>0,05) as concentrações de testosterona (1,8±0,2 vs 1,3±0,2ng/ml) e nem a de T4 (52,7±2,8 vs 50,0±2,8ng/ml). Houve declínio (P<0,01) das concentrações de T3 nos animais submetidos ao experimento (1,3±0,1 vs 1,0±0,1ng/ml), mas a redução foi observada somente nos bodes Saanen. Em ambas as raças, as concentrações de T3 e T4 variaram (P<0,01) conforme o dia da coleta das amostras de sangue. O EC foi suficiente para produzir uma resposta fisiológica com redução das concentrações plasmáticas de T3 em bodes das raças Saanen, mas não da raça Alpina, assim como não foi capaz de alterar os níveis plasmáticos de testosterona e nem de T4.

To verify the effect of heat stress (HS) on plasma testosterone, triiodothyronine (T3), and thyroxine (T4) concentrations, eight Saanen (n=4) and Alpine Brown (n=4) bucks were kept in climate chamber under thermal neutral conditions (13.0ºC to 26.7ºC) for 30 days. After a resting period (60 days), the same bucks were submitted to heat stress (23.7ºC to 34.0ºC) for another 30 days. To neutralize the seasonal variations of hormonal profiles throughout the period, the photoperiod was controlled every 30 days altering long (16 hours of light and 8 hours of darkness) and short days (8 hours of light and 16 hours of darkness). The blood samples were collected twice a week during five weeks. In both breeds, there was no effect of HS (P>0.05) on plasma concentrations of testosterone (1.8±0.2 vs 1.3±0.2ng/ml) and T4 (52.7±2.8 vs 50.0±2.8ng/ml). There was a decline (P<0.01) of plasma T3 concentrations (1.3±0.1 vs 1.0±0.1ng/ml) after HS treatment, but this reduction was only evident in Saanen bucks. In both breeds, the plasma concentrations of T3 and T4 varied (P<0.01) according to the day of blood sample collection. The HS was sufficient to provoke a physiological response with reduction of plasma concentrations of thyroid hormones mainly of T3 in Saanen bucks, but not in Alpine ones. The HS did not affect the plasma testosterone and T4 levels.

Stokes-Einstein relation for pure simple fluids.

The authors employed the equilibrium molecular dynamics technique to calculate the self-diffusion coefficient and the shear viscosity for simple fluids that obey the Lennard-Jones 6-12 potential in order to investigate the validity of the Stokes-Einstein (SE) relation for pure simple fluids. They performed calculations in a broad range of density and temperature in order to test the SE relation. The main goal of this work is to exactly calculate the constant, here denominated by alpha, present in the SE relation. Also, a modified SE relation where a fluid density is raised to a power in the usual expression is compared to the classical expression. According to the authors' simulations slip boundary conditions (alpha=4) can be satisfied in some state points. An intermediate value of alpha=5 was found in some regions of the phase diagram confirming the mode coupling theory. In addition depending on the phase diagram point and the definition of hydrodynamics radius, stick boundary condition (alpha=6) can be reproduced. The authors investigated the role of the hydrodynamic radius in the SE relation using three different definitions. The authors also present calculations for alpha in a hard-sphere system showing that the slip boundary conditions hold at very high density. They discuss possible explanations for their results and the role of the hydrodynamic radius for different definitions in the SE relation.

Annual pattern of plasma melatonin and progesterone concentrations in hair and wool ewe lambs kept under natural photoperiod at lower latitudes in the southern hemisphere.

To study the annual pattern of plasma melatonin and progesterone concentrations in hair [Santa Inês (SI)] and wool [Romney Marsh (RM) and Suffolk (SU)] ewe lambs kept under natural photoperiods at 21 degrees 59'S, 12 ewe lambs (four/breed) were used. For melatonin, blood samples were collected monthly throughout the year at the onset (17:00, 19:00 and 21:00 hr) and end (04:00, 06:00 and 08:00 hr) of the night, and for progesterone the samples were collected in the morning, two to three times a week throughout the year. Plasma melatonin concentrations at different times of the day changed according to the season. In diurnal periods (17:00 and 8:00 hr) no seasonal differences were observed but they became evident in the nocturnal intervals (21:00 and 4:00 hr) and transitional night-day (6:00 hr) times. The patterns of melatonin secretion were higher in winter and autumn than in spring and summer. The patterns of plasma progesterone secretion were affected by interaction between breed and season. There was no seasonal variation in plasma progesterone concentrations for SI females. The progesterone pattern for RM and SU females varied with season. The plasma levels were higher in autumn and winter than in spring and summer. At 21 degrees 59'S hair and wool ewe lambs showed the same annual pattern of plasma melatonin concentration while the annual progesterone profiles were quite different. For SI females this pattern was constant along all seasons and for RM and SU females this pattern was higher during autumn and winter than spring and summer.

Características do ejaculado de caprinos sob estresse calórico em câmara bioclimática / Sperm characteristics of bucks under heat stress in climatic chamber

Para verificar o efeito do estresse calórico (EC) na produção espermática de caprinos, oito machos das raças Saanen (n=4) e Pardo-Alpina (n=4) foram mantidos em câmara bioclimática, sob condições de termoneutralidade (13,0°C a 26,7°C) durante 30 dias e, após um período (60 dias) de descanso, submetidos ao EC (23,7°C a 34,0°C) por mais 30 dias. Para minimizar as variações sazonais na produção espermática, durante todo o período, o fotoperíodo foi controlado utilizando-se alternância de dias longos (16 horas de luz e 8 horas de escuro) e de dias curtos (8 horas de luz e 16 horas de escuro) a cada 30 dias. Avaliaram-se as temperaturas retal e testicular, o volume do ejaculado, a concentração espermática, as motilidades massal e individual progressiva (MIP), o vigor e a morfologia espermática. Houve aumento (P<0,05) da temperatura do testículo (31,0±1,1 vs. 32,8±0,9°C) e decréscimos (P<0,01) do volume (0,6±0,3 vs. 0,4±0,3ml), da concentração espermática (5,1±1,8 vs. 4,5±1,5 x10(9)), da motilidade massal (3,5±0,5 vs. 2,9±0,5), da MIP (67,4±14,3 vs. 53,3±13,1 por cento) e do vigor (3,5±0,6 vs.3,0±0,6) quando os animais foram submetidos ao EC. O EC não influenciou (P>0,05) o percentual total de células anormais e nem a temperatura retal. Os machos da raça Saanen apresentaram temperaturas do testículo e retal mais elevadas (P<0,01) e produziram maior volume (P<0,05) de ejaculado. O estresse calórico produzido em câmara bioclimática foi suficiente para afetar, negativamente, algumas características quanti-qualitativas do ejaculado de machos caprinos das raças Saanen e Pardo-Alpina.

To verify the effect of heat stress (HS) on caprine semen production eight male goats of Saanen (n=4) and Alpine Brown (n=4) breeds were kept in climate chamber under thermal neutral conditions (13.0°C to 26.7°C) for 30 days. After a resting period (60 days), the same bucks were submitted to heat stress (23.7°C to 34.0°C) for another 30 days. To neutralize the seasonal variations of sperm production throughout the period, the photoperiod was controlled every 30 days alterning long days (16 hours of light and 8 hours of darkness) and short days (8 hours of light and 16 hours of darkness). The following variables were evaluated: rectal and testicular temperatures, volume of ejaculate, sperm concentration, mass motility, individual progressive motility, vigor and sperm morphology. There was an elevation (P<0.01) of testicular temperature (31.0±1.1 vs. 32.8±0.9°C) and a decline of volume (0.6±0.3 vs. 0.4±0.3ml), sperm concentration (5.1±1.8 vs. 4.5±1.5x10(9)), mass motility (3.5±0.5 vs. 2.9±0.5), individual of progressive motility (67.4±14.3 vs. 53.3±13.1 percent) and vigor (3.5±0.6 vs.3.0±0.6) after HS treatment. There was no effect of HS (P>0.05) on percentage of morphologically normal spermatozoa and rectal temperature. The Saanen males showed higher testicular and rectal temperatures and produced more sperm volume than Alpine Brown males. The HS in climate chamber was sufficient to negatively affect some semen characteristics of Saanen and Alpine Brown male goats.

Effect on insulin-like growth factor-1 during in vitro oocyte maturation and in vitro culture of bovine embryos

Avaliaram-se o efeito do IGF-I na maturaçäo in vitro (MIV) (experimento I) e no desenvolvimento embrionário (DE) (experimento II) de oócitos bovinos fecundados in vitro, quanto às taxas de clivagem (TC), de blastocistos (TB) e de eclosäo(TE). Para MIV, complexos cumulus-oócitos imaturos foram cultivados em meio TCM-199 suplementado com HEPES, bicarbonato e piruvato de sódio, aditivos, soro fetal bovino (meio B-199) e gonadotrofinas 14U/ml de PMSG e 7U/ml de hCG. Para o desenvolvimento embrionário, os oócitos/zigotos foram cultivados em meio B-199 com células epiteliais do oviduto bovino em suspensäo sob óleo de silicone. As condiçöes de cultivo in vitro para ambos os experimentos seguiram os tratamentos: 1- meio B-199 + 200 ng/ml IGF-I; 2- B-199 + 100 ng/ml IGF-I; 3- B-199 + 50 ng/ml IGF-I; 4- B-199 + 10 ng/ml IGF-I; 5- B-199 + 0 ng/ml IGF-I. Todas as culturas foram realizadas a 38,5§C em atmosfera com 5(porcento) de CO2 e os dados foram analisados pelo teste do qui-quadrado. No experimento I, näo houve diferença (P>0,05) entre os tratamentos quanto às TC, TB e TE, quanto ao meio de MIV foi suplemento com IGF-I. No experimento II, a adiçäo de IGF-I ao meio de DE resultou em aumento na TC (P<0,05) mas näo influenciou a TB e a TE. A adiçäo de 200 ng/ml de IGF-I ao meio DE melhorou a TC (71,1(porcento)) quando comparada com a TC dos grupos de 100 ng/ml de IGF-I (57,6(porcento)) ou controle (56,7(porcento)), entretanto näo houve diferença quando comparada com a dos grupos de 50 ng/ml (69,4(porcento)) ou 10 ng/ml (73,1(porcento)) de IGF-I. Näo houve efeito benéfico na adiçäo de 10 a 200 ng/ml de IGF-I nos meios de MIV e de DE com relaçäo ao desenvolvimento de embriöes produzidos a partir de oócitos maturados e fecundados in vitro

Avaliaçäo das condiçöes de maturaçäo oocitária e do efeito do reprodutor na produçäo in vitro de embriöes bovinos / Evaluation of oocyte maturation conditions and bull effect on the in vitro bovine embryo production

Avaliaram-se as condiçöes de cultura para maturaçäo dos oócitos (Exp. I) e o efeito do reprodutor (Exp. II) sobre as taxas de clivagem (TC) e de mórulas e blastocistos (MO/BL) produzidos in vitro. Oócitos imaturos foram submetidos a maturaçäo in vitro sob diferentes condiçöes: meio B-199, acrescido de 5 por cento de soro de vaca em estro (SVE), 5 por cento de soro fetal bovino (SFB) e células da granulosa (T1 subscrito/Exp. I) ou meio B-199, acrescido de 10 por cento de SFB, 14 UI/ml de PMSG e 7 UI/ml de hCG (T2 subscrito/Exp I). Após 24 h de cultura, os oócitos maturos foram inseminados com sêmen descongelado de dois reprodutores (R1 subscrito e R2 subscrito/Exp. II) e, após 48 h de incubaçäo, os embriöes de 2 e 4 células foram transferidos para placas de cultivo in vitro, onde permaneceram em cultura por mais 9 dias. No Exp. I, os oócitos de T1 subscrito e T2 subscrito foram inseminados com sêmen do R1 subscrito/Exp. II. No Exp. II, os oócitos do T1 subscrito/Exp. I foram inseminados com sêmen de R1 subscrito e R2 subscrito/Exp. II. No Exp. I, a TC foi superior (p<0,0l) para T2 subscrito, quando comparado com T1 subscrito. A produçäo de MO/BL näo foi diferente (p>0,05) entre tratamentos. No Exp. II, a TC e a taxa de MO/BL diferiram (p<0,05) para cada reprodutor. A adiçäo de hormônios no meio de maturaçäo, embora näo tenha interferido na produçäo de embriöes, parece ser um procedimento mais prático que o uso de células da granulosa. A utilizaçäo de sêmen de diferentes reprodutores afetou o subseqüente desenvolvimento embrionário in vitro