Use of alternative diluent ACP-Lact® and coconut water powder (ACP) in cryopreservation of goat semen and fixed-time artificial insemination (FTAI) in half-breed goats.

The aim of the present study was to evaluate semen cryopreservation with ACP-Lact® diluent, which consists of coconut water powder (ACP) added to goat milk powder. After thawing, the samples were evaluated for sperm kinetics, membrane evaluation and in vivo insemination. For cryopreservation, a pool was made with the ejaculate of six goats, diluted in four equal aliquots for the respective treatments: T1 (ACP-Lact®); T2 (ACP-Lact® 50%); T3 (ACP + 2.5% egg yolk) and T4 (Tris + 2.5% egg yolk). After dilution of the treatments, the samples were placed in 0.5 ml straws and chilled at a rate of -1.07°C/min. After reaching 4°C and stabilizing for one hour, the straws were placed in nitrogen vapour at -60°C for 15 minutes and then immersed in liquid nitrogen (-196ºC). The straws were thawed in a 37°C water bath and kinetic assessments were performed immediately using a computerized semen analysis program (CSA), viability (EN), membrane functionality (HOST), mitochondrial activity (DAB) and DNA integrity assessment of spermatozoa. For the in vivo experiment, ten goats were inseminated, divided into two groups of five goats each, G1 inseminated with ACP-Lact® and G2 with ACP, by fixed-time artificial insemination (FTAI). Regarding the kinetic parameters, the ACP-Lact® treatment showed higher progressive motility (PM) and sperm velocity than the other treatments (36.77%). In the VSL parameter the ACP-Lact diluent was superior to ACP and Tris. In viability the treatment with ACP-Lact® was superior to the treatment with Tris, 95% and 83% respectively. In FTAI two goats were born out of the 5 goats inseminated with ACP-Lact®. It was concluded that the use of ACP-Lact® for cryopreservation of caprine semen is efficient in maintaining seminal parameters during thawing in vitro and in vivo and proved to be a good alternative extender for the caprine species.

Assessment of coconut water added to Numida meleagris egg yolk as cryoprotectant for goat semen.

Effects were assessed of the dilutants TRIS and ACP - 101c® with the addition of different guinea fowl (Numida meleagris) egg yolk concentrations. Fifteen ejaculates were collected from five goats of the Anglo Nubian breed. The ejaculates were pooled and then divided into 12 groups, two control groups (GC1 TRIS, with 2.5% Gallus gallus domesticus hen egg yolk GOGD), (GC2 Control Group ACP - 101c®, with the addition of 2.5% Gallus gallus domesticus hen egg yolk GOGD) and ten experimental groups (EG), containing TRIS and ACP added with different concentrations of egg yolk from guinea hen (Numida meleagris) (TRIS 2,5% GONM; TRIS 5% GONM; TRIS 10% GONM; TRIS 15% GONM; TRIS 20% GONM; ACP® 2,5% GONM; ACP® 5% GONM; ACP® 10% GONM; ACP® 15% GONM; ACP® 20% GONM). Then cryopreservation was carried out and the samples stored in liquid nitrogen (-196 °C). After seven days, the samples were thawed and assessed for spermatic kinetics, immunofluorescence and sperm morphology. Analysis of GOMN by the CASA system showed that the various parameters were similar to those of GOGD (P>0.05). The membrane integrity, mitochondrial potential and the acrosome were not influenced by the treatment (P>0.05) nor by the dilutant used for cryopreservation (P>0.05). The spermatic morphology was also preserved by the different GOGD and GONM concentrations in the ACP® and TRIS dilutants, with no statistically significant differences (P<0.05). It was concluded that Numida meleagris egg yolk, as external membrane cryoproctant added to the dilutants ACP-101c® and TRIS, improved goat semen quality.

Extra Virgin Coconut Oil as a Cryoprotector for Cryopreservation of Caprine Semen.

The study aimed to evaluate the effect of powdered coconut water-based diluent (ACP-101c) associated with extra virgin coconut oil (CO) as an external cryoprotectant in the conservation of cryopreserved buck sperm. For cryopreservation, the ejaculates from four bucks were pooled and divided into three aliquots and diluted at 37°C for treatments T1 (ACP-101c + 2.5% egg yolk +7% glycerol), T2 (ACP-101c + 2.5% CO +7% glycerol), and T3 (ACP-101c + 5% CO +7% glycerol). Then, the samples were packaged and cooled at a rate of 1.07°C/min decrease. Upon reaching 4°C, the samples were stored in a refrigerator at 4°C for 30 minutes for stabilization. After this period, the straws were frozen in nitrogen vapor for 15 minutes and then immersed and stored in liquid nitrogen at -196°C. After thawing, the samples were evaluated for sperm kinetics, plasma membrane integrity, acrosomal integrity, membrane functionality, mitochondrial activity (MA), and sperm morphology. In this study, no statistically significant differences were observed between the three treatments regarding the kinetic parameters (p > 0.05; Table 1). However, in relation to the velocities, a reduction was observed beyond the expected. There were no statistically significant differences between the diluents T1, T2, and T3 for the three velocities (curvilinear velocity [VCL], linear velocity [VSL], average path velocity [VAP]). Furthermore, no statistically significant differences were observed (p > 0.05) among treatments regarding the evaluation of membrane integrity, the functional membrane, MA, and sperm morphology after thawing. In conclusion, the use of CO in concentrations of 2.5% and 5.0% is effective in maintaining goat sperm quality, presenting itself as an alternative diluent for international programs of artificial insemination and embryo transfers. [Table: see text].

Human cornea conservation in coconut water solution / Conservação de córneas humanas em solução de água de coco

ABSTRACT Purpose: The aim of this study was to evaluate the physical and chemical characteristics of coconut water and to analyze the use of coconut water solution for the conservation of human corneas. Methods: This was an experimental and controlled study performed at the Eye Bank of the General Hospital of Fortaleza. The coconut water-based solution was prepared at the Goat Seed Technology Laboratory of the Department of Veterinary Medicine of the State University of Ceará. Discarded corneas from the Eye Bank were divided into two groups for sequential experiments: G1, coconut water-based solution (experimental group), and G2, conservative treatment with OPTISOL GS® (control group). The osmolality of corneas in G1 was analyzed sequentially at 275, 300, 325, 345, 365, and 400 mOsm/L. The viability of the corneas was determined by specular microscopy and biomicroscopy on the first, third, and seventh days. Results: Corneas preserved in a solution of 365 and 345 mOsm/L had a transparency of 8 mm until the third day and had diffuse edema in the periphery, central folds, and partial epithelium loss until the seventh day. The 365-mOsm/L solution was associated with the worst results during follow-up. Corneas placed in Optisol-GS retained their original aspects. Conclusions: Coconut water-based preservative partially maintained corneal transparency and epithelial integrity, especially during the first three days of follow-up. The coconut water-based solutions used were not effective for use as preservatives in a human eye bank.(AU)

RESUMO Objetivos: As características físico-químicas e o baixo custo da água de coco foram fundamentais para o este estudo. Analisar o uso de solução a base de água de coco como meio de conservação de córneas humanas em banco de olhos. Métodos: Estudo experimental e controlado realizado no Banco de Olhos do Hospital Geral de Fortaleza. Utilizou-se solução à base de água de coco preparada no laboratório de Tecnologia de Sêmen de Caprinos do Departamento de Medicina Veterinária da Universidade Estadual do Ceará. Foram usadas córneas de descartes divididas em dois grupos: G1 (Conservante com água de coco) - grupo experimental e G2 (grupo Conservante com OPTISOL GS®) grupo controle, em experimentos sequenciais. A osmolaridade do G1 foi analisada sequencialmente com 275, 300, 325, 345, 365 e 400 mOsm/L. A viabilidade das córneas foram realizadas por microscopia especular e biomicroscopia nos 1º, 3º e 7º dias. Resultados: As córneas em solução de 365 e 345 mOsm/L apresentavam transparência nos 8mm centrais até o 3º dia, com edema em toda periferia, dobras centrais e edema 2+, com perda parcial do epitélio até 7º dia, sendo o de maior osmolaridade com melhor transparência durante o seguimento. Grupo com 275, 300 e 400 mOsm/L, córnea opaca, edema difuso, perda total do epitélio no 3º dia. As córneas em Optisol mantiveram seus aspectos. Conclusões: O conservante à base de água de coco manteve em parte a transparência corneana e a integridade epitelial, especialmente nos primeiros 3 dias de seguimento. A solução conservante com água de coco nas formulações utilizadas não se mostrou eficaz para o uso em banco de olhos humanos.(AU)

Human cornea conservation in coconut water solution.

PURPOSE: The aim of this study was to evaluate the physical and chemical characteristics of coconut water and to analyze the use of coconut water solution for the conservation of human corneas. METHODS: This was an experimental and controlled study performed at the Eye Bank of the General Hospital of Fortaleza. The coconut water-based solution was prepared at the Goat Seed Technology Laboratory of the Department of Veterinary Medicine of the State University of Ceará. Discarded corneas from the Eye Bank were divided into two groups for sequential experiments: G1, coconut water-based solution (experimental group), and G2, conservative treatment with OPTISOL GS® (control group). The osmolality of corneas in G1 was analyzed sequentially at 275, 300, 325, 345, 365, and 400 mOsm/L. The viability of the corneas was determined by specular microscopy and biomicroscopy on the first, third, and seventh days. RESULTS: Corneas preserved in a solution of 365 and 345 mOsm/L had a transparency of 8 mm until the third day and had diffuse edema in the periphery, central folds, and partial epithelium loss until the seventh day. The 365-mOsm/L solution was associated with the worst results during follow-up. Corneas placed in Optisol-GS retained their original aspects. CONCLUSIONS: Coconut water-based preservative partially maintained corneal transparency and epithelial integrity, especially during the first three days of follow-up. The coconut water-based solutions used were not effective for use as preservatives in a human eye bank.

Sêmen ovino e caprino imunossexado e diluído em meio de conservação à base de água de coco em pó (ACP101/102c) / Ram and goat semen immunosexed and diluted in powdered coconut water-based preservation medium (ACP101/102c)

Sperm sexing aims to separate sperm populations in carriers of the "X" or "Y" chromosome. Currently, flow cytometry is a technique that allows greater accuracy; however, it causes structural changes in sperm, reduces viability, and has a high cost. As a result, other methods have been researched, including immunosexing, which uses monoclonal antibodies to detect sex-specific surface antigens. Thus, the objective of this study was to evaluate the immunosexing technique using a monoclonal antibody against sex-specific protein (HY) in the conservation of ram and goat semen in ACP101/102c. Ejaculates from five rams and five goats were collected with the aid of an artificial vagina; they were evaluated and submitted to the immunosexing protocol, according to the manufacturer's recommendations, using the Monoclonal Antibody Kit specific for mammalian sperm with "Y" chromosomes (HY; HY Biotechnology, Rio de Janeiro, RJ, Brazil). After sexing, the supernatant was resuspended in the cryopreservation diluent: ACP ram (ACP101/102c + 20% egg yolk + 7% glycerol) and ACP goat (ACP101/102c + 2.5% egg yolk + 7% glycerol), packaged in 0.25 mL straws, refrigerated at 4°C, stabilized for 30 min, frozen in liquid nitrogen vapor (-60°C) for 15 min, immersed in liquid nitrogen, and stored in cryogenic cylinders. The samples were evaluated in natura (T1), after immunosexing (T2) and after thawing (T3) for sperm motility subjectively using conventional microscopy (40x). Plasma membrane integrity (IMP) and sperm cell morphology were evaluated by the smear staining technique using eosin-nigrosine dye, and the percentages of healthy and morphologically defect spermatozoa were determined. In the evaluation of ram semen regarding sperm motility and IMP, no statistically significant differences were observed between treatments after sexing in the evaluation of absolute data (P > 0.05), with the difference being observed only between T1 and T2, and T3 (P < 0.05). Regarding the relative percentage and sperm morphology, no statistically significant differences were observed (P > 0.05). Regarding the evaluation of goat semen samples, the motility parameters were consistent with the technique submitted; however, the IMP data did not appear as expected, requiring further evaluation for a better assessment of the technique for this species. The data obtained from ram semen submitted to the immunosexing protocol, regarding the absolute evaluation of motility and IMP, demonstrated that the non-sexed semen (T1) was superior to the sexed treatments (T2 and T3); however, it is noteworthy that freezing started with approximately 50% of the cells, since the immunosexing technique results in a loss of viability of approximately 50% of the sperm, which corresponds to the ratio of sperm carrying the X chromosome. In addition, when the data in this study were transformed into relative values, no statistical differences were observed, indicating that the immunosexing protocol, as well as the freezing protocol, did not significantly affect the quality of ram sperm cells. In relation to the immunosexing of goat semen, future studies should be conducted in vitro to define a more appropriate protocol for the species and, in addition, in vivo studies should be performed to prove the quality of the technique. It was concluded that the immunosexing process using a monoclonal antibody against sex-specific protein (HY) associated with the use of powdered coconut water diluent (ACP101/102c) in the cryopreservation of semen proved to be efficient in the in vitro evaluation of ovine species.(AU)

Alterações posturais: a caracterização de discentes de Fisioterapia em uma instituição do ensino superior em Fortaleza/CE / Postural changes: the characterization of Physiotherapy students in a higher education institution in Fortaleza/CE

Na postura padrão, a coluna apresenta curvaturas normais e os ossos dos membros inferiores ficam em alinhamento. Quando o componente estrutural é alterado, o corpo humano modifica-se para desempenhar tal situação da melhor forma possível, o que pode ocasionar em um desvio postural. O objetivo desta pesquisa é avaliar a postura e seus comprometimentos em discentes de um curso de Fisioterapia, traçando o perfil clínico socioeconômico, conhecendo os comprometimentos posturais dos participantes da pesquisa. Tratou-se de um estudo transversal, descritivo e quantitativo realizado entre os meses de agosto de 2015 a junho de 2016, no Centro Universitário Estácio do Ceará com 32 discentes do curso de Fisioterapia. Os dados foram coletados através de uma ficha de avaliação postural desenvolvida para o inquérito e analisada no programa Excel® 2013 e confrontados com a literatura vigente sobre o assunto. O gênero feminino foi predominante em 75% da amostra. Em relação ao estado civil dos participantes, 87,5% eram solteiros. A média de idade foi de 24,4 anos. Em relação ao Índice de Massa Corpórea, foi evidenciado que 28 participantes (87,5%) apresentaram um peso normal, de acordo com sua altura e peso. Para verificar a presença de escoliose, foi realizado o Teste de Adams. Evidenciou-se que 72% dos participantes apresentaram gibosidade, 12,50% apresentaram gibosidade lombar, 43,75% apresentaram gibosidade torácica e 15,63% apresentaram gibosidade toracolombar. A maioria dos estudantes apresentou escoliose. No entanto, estudos com uma amostra maior devem ser realizados, a fim de que resultados mais abrangentes possam ser obtidos. (AU)

In the standard posture, the spine has normal curvatures and the bones of the lower limbs are in alignment. When the structural component is changed, the human body changes to perform this situation in the best possible way, which can cause a postural deviation. The objective of this study was to evaluate the posture and its commitments in students of a Physical therapy course, tracing the socioeconomic clinical profile, knowing the postural impairments of the participants. This was a cross-sectional, descriptive and quantitative study carried out between August 2015 and June 2016, at the Estácio do Ceará University Center with 32 students. The data were collected through a postural assessment form developed for the survey and analyzed using the Excel® program and compared with the current literature. The female gender was predominant in 75% of the sample. Regarding the participants' marital status, 87.5% were single. The average age was 24.4 years. Regarding the Body Mass Index, it was evidenced that 28 participants (87.5%) had a normal weight, according to their height. To test for the presence of scoliosis, the Adams Test was performed. 72% of the participants presented gibosity, 12.50% lumbar gibosity, 43.75% thoracic gibosity and 15.63% thoraco-lumbar gibosity. Most of the students had scoliosis. However, studies with a larger sample should be carried out to obtain more accurate results. (AU)

Coconut Water as an Extender Component for Cooled Equine Sperm.

The aim of this study was to evaluate the effect of coconut water as a component of extender in different formulations for cooling equine sperm. One ejaculate of fourteen stallions was collected. Sperm was diluted to 50 × 106 sperm/mL using five different extenders: ACP-105: powdered coconut water extender (ACP-105, ACP Biotecnologia, Brazil); ACP-Milk: ACP-105 + 20 g/L of skimmed milk; ACP-EY 2.5%: ACP-105 + 2.5% of egg yolk; ACP-EY 5%: ACP-105 + 5% of egg yolk; and BotuSêmen (Botupharma, Botucatu, Brazil) and cooled in passive cooling device (BotuFlex, Botupharma, Botucatu, Brazil) at 5 and 15°C for 24 hours. Sperm kinetics and plasma membrane integrity (PMI) were evaluated by computer-assisted sperm analysis and fluorescence staining, respectively, at T0 (before cooling) and T24 (24 hours after cooling). Sperm kinetics did not differ at T0 among groups (P > .05); however, at T24, these parameters were significantly lower in ACP-105 (5°C, total motility [TM]: 9.2 ± 3.6%; progressive motility [PM]: 2.7 ± 1.6%; percentage of fast-moving spermatozoa [RAP]: 4.8 ± 3.0%; 15°C, TM: 10.6 ± 3.0%; PM: 1.1 ± 0.5%; RAP: 4.8 ± 1.9%) and ACP-EY 5% (5°C, TM: 28.0 ± 6.3%; PM: 5.7 ± 1.8%; RAP: 15.9 ± 6.0%; 15°C, TM: 30.0 ± 6.0%; PM: 6.9 ± 2.1%; RAP: 17.6 ± 5.3%) compared with BotuSêmen (5°C, TM: 66.2 ± 5.6%; PM: 21.1 ± 2.8%; RAP: 53.9 ± 6.1%; 15°C, TM: 63.4 ± 5.4%; PM: 17.2 ± 2.8%; RAP: 51.4 ± 6.3%) (P < .05). All groups exhibited similar PMI at tested moments and cooling temperatures (5°C: 83%; 15°C: 84%) (P > .05). Further studies are necessary to evaluate powdered coconut water in different compositions of sperm extender; however, coconut-based extender as used in this study was not an alternative to preserve sperm parameters of cooled equine sperm.

Estudo comparativo da prevalência de alterações posturais na coluna vertebral em escolares do ensino fundamental do município de Quixadá/CE / Comparative study of the impact of postural changes on spine in elementary school of Quixadá/CE

Introdução: A má postura caracteriza-se pela relação defeituosa entre as várias partes do corpo que produz uma maior tensão nas estruturas de apoio. Objetivo: Comparar a prevalência de alterações posturais da coluna vertebral em alunos do ensino fundamental de duas escolas, uma da rede privada e outra da rede pública, do município de Quixadá/CE. Métodos: Avaliaram-se 40 alunos voluntários de ambas as escolas, sendo 48% do sexo masculino e 52% do sexo feminino, com idades entre 11 e 15 anos. Analisaram-se com ajuda de bolas de isopor sobrepostas nos principais relevos anatômicos e em seguida fotografias, nas quatro vistas, anterior, posterior, lateral esquerda e lateral direita, de forma estática, posicionados atrás do simetrógrafo, analisando através do software Coreldraw, marcando as alterações mais evidentes. Resultados: Demonstraram a saúde deficiente da coluna vertebral em escolares, com a identificação de várias alterações posturais, sendo mais prevalente na instituição da rede municipal de Quixadá/CE. Sendo elas: hipercifose, desequilíbrio pélvico, desequilíbrio escapular, inclinação lateral cervical, anteriorização cervical e elevação unilateral do ombro. Entretanto, os alunos da instituição da rede privada apresentaram as mesmas alterações, sendo em um menor índice. Conclusão: Observou-se que o fator socioeconômico das instituições e dos alunos que as compõe pode provocar futuras alterações posturais, devido às mobílias e a forma de transporte de materiais serem inadequadas. O estudo sugere a presença de um fisioterapeuta no ambiente escolar onde seria possível intervir na evolução dessas alterações e a fixação dos desvios, visando o trabalho preventivo e educacional. (AU)

Introduction: Bad posture is characterized by the defective relationship between the various parts of the body that produces a greater tension in the supporting structures. Objective: To compare the prevalence of postural alterations of the spine in elementary school students from two schools, one private and another public, from the municipality of Quixadá/CE. Methods: A total of 40 students from both schools were evaluated, 48% male and 52% female, aged 11 to 15 years. We analyzed with the aid of styrofoam balls overlapped in the main anatomical reliefs and then photographied, in the four views, anterior, posterior, left lateral and right lateral, in a static way, positioned behind the symetrograph, analyzing through Coreldraw software, marking the most evident changes. Results: The results showed poor health of the spine in schoolchildren, with the identification of several postural alterations, being more prevalent in the public institution. These include: hyperkyphosis, pelvic imbalance, scapular imbalance, cervical lateral inclination, anterior cervical and unilateral shoulder elevation. However, the students from the private institution showed the same changes, but in a lower level. Conclusion: We observed that the socioeconomic factor of institutions and students can cause future postural alterations, due to the furniture and the inadequate way of transportation of school materials. The study suggests the presence of a physiotherapist in the school environment where it would be possible to modify the evolution of these alterations and the establishment of deviations, aiming at preventive and educational work. (AU)

Vitamin E (Trolox) addition to Tris-egg yolk extender preserves ram spermatozoon structure and kinematics after cryopreservation.

Several studies reveal that vitamin E acts as a cellular stabilizer of unsaturated lipids against oxidative deterioration, thus maintaining structural and functional integrity at the subcellular level. The objective of this study was to evaluate Vitamin E (Trolox) addition to freezing extender for ram spermatozoa. Semen samples were diluted in Tris-yolk egg medium without antioxidant (control group) and with Trolox in different concentrations (30, 60 and 120µM). After thawing (37°C/30s), samples were subjected to analysis for plasma membrane integrity (PMi), acrosome integrity (Aci), mitochondrial membrane potential (MMP), sperm kinematics, and ultrastructural integrity. The Trolox 60 and 120µM groups showed higher percentages of iPMs (P<0.05) when compared to the control group. Differences were observed among groups in sperm kinematic indicators (progressive motility, linearity, straightness, oscillation index, straight-line velocity and average path velocity), with higher values (P<0.05) for the Trolox 60 and 120µM groups. On ultrastructural assessment, Trolox addition at the three concentrations preserved spermatozoon head plasma membranes, while for the spermatozoon tail, plasma membrane preservation at 60µM was higher (P<0.05) than the other groups. The Trolox 60 and 120µM groups presented more mitochondrial ultrastructural preservation than the other groups (P<0.05). These results indicate that Trolox addition to Tris-egg yolk at 60 and 120µM provides greater structural integrity (plasma membrane and mitochondria) and kinematics for ram spermatozoa after cryopreservation.

Espermatozoides caprinos criopreservados em meio à base de leite desnatado acrescido de glutationa reduzida / Goat spermatozoa after freezing in skimmed-milk extender supplemented with reduced glutathione

Visando avaliar o efeito da adição de glutationa reduzida (GSH) ao diluente de congelação de sêmen caprino à base de leite desnatado, utilizou-se sêmen de cinco reprodutores Boer. Após colheita e avaliação, procedeu-se à formação do pool dos ejaculados e diluição em leite desnatado e glicerol 7 por cento, acrescido de antioxidantes: G1) Controle; G2) GSH 2mM mL-1; G3) GSH 5mM mL-1 e G4) GSH 7mM mL-1. As amostras foram congeladas em palhetas (0,25mL) e armazenadas a -196°C. Após descongelação, avaliou-se a integridade de membrana plasmática (iMP) e acrossomal (iAc), potencial de membrana mitocondrial (PMM), cinética e ultraestrutura. Os grupos Controle e GSH (2, 5 e 7mM mL-1) não diferiram (P>0,05) em iMP, iAc, PMM e cinética. Na análise ultraestrutural, os porcentuais de membrana plasmática (cabeça e cauda) e acrossoma íntegros não diferiram (P>0,05) entre grupos. Todavia, o grupo Controle apresentou maior porcentual (P<0,05) de gametas com axonema íntegros do que os de GSH (2, 5 e 7mM mL-1). Maior porcentagem (P<0,05) de espermatozoides com mitocôndrias íntegras foi observada no grupo Controle do que nos de GSH (5 e 7 mM mL-1). Conclui-se que a adição de GSH (2, 5 e 7mM mL-1) em diluente de congelação de sêmen caprino, à base de leite desnatado, não preserva a integridade dos espermatozoides.

Aiming to evaluate in vitro effect of different concentrations of glutathione reduced (GSH) in skimmed-milk and glycerol 7 percent it was used semen from five Boer bucks. After collect and evaluation, a pool of samples was diluted in skimmed-milk and glycerol 7 percent plus antioxidant: G1) Control; G2) GSH 2mM mL-1; G3) GSH 5mM mL-1 and G4) GSH 7mM mL-1. Samples were frozen in straws (0.25mL) and stored at -196°C. After thawing, samples were subjected to integrity of the plasma membrane (iMP) and acrosomal (iAc), mitochondrial membrane potential (MMP), kinematic and ultrastructure analysis. Control and GSH (2, 5 and 7mM mL-1) groups did no differ (P>0.05) in iMP, iAc, PMM and kinematic parameters. In the ultrastructural analysis, percentages of acrosome and plasma membrane (tail and head region) intact did not differ (P>0.05) between groups. However, Control group had higher percentage (P<0.05) of gametes with intact axonemes than those of GSH (2, 5 and 7mM mL-1) groups. Higher percentage (P<0.05) of sperms with intact mitochondrias were observed on Control group than those of GSH (5 and 7mM mL-1). It can be concluded that the GSH (2, 5 and 7mM mL-1) addition in skimmed-milk diluent to freeze goat semen did not preserve sperm integrity.

Fertilidade após a inseminação artificial intra-cervical ou laparoscópica intra-uterina de ovelhas utilizando diluidores à base de água de coco / Fertility following intracervical or intrauterine laparoscopic insemination of ewes using extenders based on coconut water

O objetivo deste estudo foi avaliar a taxa de prenhez em ovelhas utilizando diluidores à base de água de coco (in natura: ACN ou em pó: ACP-102®) após inseminação artificial intra-cervical (Experimento 1) ou laparoscópica intra-uterina (Experimento 2). Experimento 1. Sêmen de 4 carneiros Santa Inês foi coletado, diluído a 37°C (T1: ACN; T2: ACP-102®) e resfriado á 4°C. 56 ovelhas Santa Inês foram inseminadas cervicalmente após a sincronização, 31 utilizando o diluidor ACN e 25 o diluidor ACP-102®. Experimento 2. Sêmen de 5 carneiros adultos (Santa Inês: n=04; Dorper n=01) foi coletado e processado de acordo com o descrito. 64 ovelhas SRD foram inseminadas intra-uterina por laparoscopia após a sincronização do estro, 37 utilizando o diluidor ACN e 27 o diluidor ACP-102®. O diagnóstico de gestação foi realizado por ultra-sonografia. A taxa de prenhez entre os tratamentos, dentro de cada método de inseminação, entre cada diluidor para ambos métodos de inseminação foi analisada pelo teste do Qui-quadrado (p<0,05). A taxa de prenhez após IA intra-cervical (ACN: 25,8% vs. ACP-102®: 48%) e laparoscópica (ACN: 72,9% vs ACP-102®: 70,3%) não foi influenciada pelos diluidores. A taxa de prenhez foi influenciada pelo método de inseminação (intra-cervical: 35,7% vs.laparoscopia: 71,8%; p<0,05). Os diluidores a base de água de coco podem ser utilizados nas inseminações artificiais cervical ou laparoscopica em ovelhas do Nordeste do Brasil em condições de campo.

The objetive of this study was to evaluate pregnancy rates in ewes using extenders based on coconut water (in natura: NCW or in powder: PCW-102®) following intra - cervical (Trial 1) or intrauterine laparoscopic insemination (Trial2). Trial 1. Semen from 4 Santa Inês rams were collected, diluted at 32°C (T1: NCW; T2: PCW-102®) and cooled to 4°C. 56 adult Santa Inês ewes were inseminated intra-cervically following syncronization, 31 using the extender NCW and 25 the extender PCW-102®. Trial 2. Semen from 5 rams (Santa Inês: n=04; Dorper n=01) were collected and processed as described. 64 adult crossbred multiparous ewes were inseminated intrauterine by laparoscopy following oestrus syncronization. 37 ewes using the extender NCW and 27 the extender PCW-102®. The pregnancy diagnosis was performed by ultrasonography. The fertility rates between treatments for each method of insemination and within each extender for both methods were analysed by Chi-square test (p<0,05). The pregnancy rates following intra-cervical (NCW: 25.8% vs PCW-102®: 48%) and intrauterine (NCW: 72.9% vs 70.3%) inseminations were not influenced by the extenders. The pregnancy rate was influenced by insemination method (intra-cervical: 35.7% vs laparoscopy: 71.8%; p<0,05). The extenders based coconut water as basis can be used following cervical or intra-uterine laparoscopic inseminations in ewes from Northeast of Brazil under field conditions.

Parâmetros biométricos do trato genital masculino de caprinos sem raça definida (SRD) criados no semi-árido nordestino durante o período seco e chuvoso / Biometry from crioula goat male reproductive in northeastern semi-arid during season dry or rainy

Este trabalho teve por objetivo comparar a morfometria do trato genital masculino caprino entre a época seca e chuvosa. Foram coletados 46 e 52 genitais de machos caprinos na época seca e chuvosa, respectivamente. Testículos foram identificados em direito ou esquerdo, mensurados quanto ao comprimento, espessura e diâmetro. Os epidídimos foram pesados. Ductos deferentes e o pênis foram mensurados quanto ao comprimento. As vesículas seminais foram identificadas em direita ou esquerda, pesadas individualmente, e mensuradas quanto ao comprimento, largura e espessura. Os parâmetros de peso, largura, espessura e comprimento das diferentes estruturas foram submetidos ao teste t de Student a 5,00 por cento de probabilidade. Os resultados demonstraram que houve diferença significativa entre os parâmetros mensurados no período seco e chuvoso (P<0,05), com exceção da vesícula seminal. Também foi demonstrado que os maiores valores foram encontrados no período seco, com exceção do ducto deferente. Concluiu-se que os parâmetros biométricos de caprinos SRD da região semi-árida do Nordeste do Brasil são inferiores aos citados na literatura internacional. Estes resultados demonstraram que o processo de adaptação de raças exóticas trazidas pelos colonizadores portugueses ao longo destes 500 anos provocou uma diminuição do porte dos mesmos, tornando-os mais rústicos, porém com características reprodutivas normais, mesmo em épocas de escassez de alimentos.