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1.
Biosci. j. (Online) ; 33(6): 1617-1621, nov./dec. 2017. ilus, tab, graf
Article in English | LILACS | ID: biblio-966524

ABSTRACT

The ability of bryophytes to tolerate salt is determined by a number of biochemical routes, whereas the salt ends up driving the activation of adaptive responses to tolerate this adverse condition. Salinity is the main limiting environmental factor under plant development, and is caused by excess salt ions in the environment, mainly Na + and Cl-. The optimal growth of plants in saline environment is obtained in concentrations of 50% of NaCl. Due to these findings, the importance of the study of the effect of salinity on the germination of plants, in this case in Funaria hygrometrica Hedw., is noticed.


A capacidade das briófitas para tolerar meios salinos é determinada por uma série de vias bioquímicas, uma vez que o sal acaba por conduzir a ativação de respostas adaptativas para tolerar esta condição adversa. A salinidade é o principal fator ambiental limitante no desenvolvimento da planta e é causada pelo excesso de íons salinos no ambiente, principalmente Na+ e Cl-. O crescimento ótimo de plantas em ambiente salino foi obtido em concentrações de 50% de NaCl. Devido a essas descobertas esses achados, observa-se a importância do estudo do efeito da salinidade sobre a germinação de plantas, neste caso em Funaria hygrometrica Hedw.


Subject(s)
In Vitro Techniques , Bryophyta , Salt-Tolerant Plants/growth & development
2.
Arq. bras. med. vet. zootec ; 66(2): 411-416, Jan.-Apr. 2014. ilus, tab
Article in English | LILACS | ID: lil-709278

ABSTRACT

The objectives of this study were to investigate whether TGF-β affect the survival, activation and further growth of goat primordial follicles enclosed in ovarian cortex after in vitro culture. Goat ovaries were collected from an abattoir and pieces of ovarian tissues were cultured for one or seven days in a supplemented alpha Minimum Essential Medium, alone or containing TGF-β (1, 5, 10 or 50ng/mL). Ovarian tissues from the fresh control as well as those cultured were processed for histological and ultrastructural studies. The results showed that when compared with fresh control, there was decrease in the percentages of histologically normal follicles in all treatments only after seven days culture. TGF-β did not affect the activation of preantral follicles regardless of its concentration, however, larger follicles diameter (P<0.05) was observed using 10ng/mL TGF-β than in the fresh control and other treatments. Moreover, this concentration maintained the normal ultrastructure after seven days of culture. In conclusion, TGF-β showed additional effect on the follicle growth and the maintenance of ultrastructural integrity of goat preantral follicles enclosed in ovarian tissue when used at 10ng/mL during seven days of culture...


O objetivo desse estudo foi investigar se o TGF-β afeta a sobrevivência, ativação e crescimento de folículos primordiais caprinos inclusos no córtex ovariano após o cultivo in vitro. Ovários de cabras foram coletados em abatedouro e fragmentos de tecido ovariano foram cultivados por um e sete dias em meio essencial mínimo alfa (α-MEM+) sozinho ou suplementado com TGF-β (1, 5, 10 ou 50ng/mL). Fragmentos ovarianos não cultivados e cultivados foram processados para análise histológica e ultraestrutural. Os resultados mostraram que, comparado ao controle fresco, houve diminuição no percentual de folículos morfologicamente normais em todos os tratamentos somente após sete dias de cultivo. O TGF-β não afetou a ativação folicular independente da concentração testada, contudo, o diâmetro folicular foi superior (P<0.05) no tratamento com 10ng/mL de TGF-β quando comparado ao controle fresco e aos demais tratamentos. Além disso, essa mesma concentração manteve a ultraestrutura normal dos folículos após sete dias de cultivo. Em conclusão, o TGF-β apresentou efeito adicional no crescimento folicular e na manutenção da integridade ultraestrutural de folículos pré-antrais caprinos inclusos no tecido ovariano quando utilizado na concentração de 10ng/mL durante sete dias de cultivo...


Subject(s)
Animals , Female , Goats/embryology , Transforming Growth Factor beta/administration & dosage , Ovarian Follicle , Biometry , Ovarian Follicle/growth & development
3.
Journal of Veterinary Science ; : 73-78, 2003.
Article in English | WPRIM | ID: wpr-36638

ABSTRACT

In this study, we examined the effects of a two-step culture system, which involves the use of different culture media for early cleavage and later stage embryos, on the in vitro development of bovine embryos. We also investigated the effect of glucose, phosphate and citrate on the in vitro early developmental period of bovine embryos in a two-step culture system. Moreover, the supplementation of different protein sources (BSA-V, BSA-FAF and FBS) during IVC did not affect the frequency of blastocyst development. Using two-step culture, embryos were cultured in protein-free media for an initial 5 days. This was then followed by the same culture media or an FBS supplemented media. The developmental rates of blastocysts in the FBS containing group were significantly higher than in the replaced with no serum containing group. Embryos cultured in mSOF supplemented with 1.5 mM glucose plus 1.2 mM phosphate were significantly inhibited. The inhibition of developmental competence by glucose plus phosphate was consistent with the existence of 0.5 mM sodium citrate. This study indicates that a two-step culture system, which applies different conditions for early cleavage embryos, i.e., serum-free media, vs. later stage embryos, with serum containing media, may be effective for in vitro production systems. In addition, the developmental competence of bovine embryos was depressed in the presence of glucose plus phosphate as compared to either alone or the absence of both. Therefore, the avoidance of this negative effect should allow more optimal conditions to be developed for in vitro production.


Subject(s)
Animals , Female , Male , Blastocyst/drug effects , Cattle/embryology , Citric Acid/pharmacology , Culture Media/chemistry , Culture Techniques/methods , Ectogenesis/drug effects , Embryonic Structures/drug effects , Embryonic and Fetal Development/drug effects , Energy Metabolism , Fertilization in Vitro , Glucose/pharmacology , Phosphates/pharmacology , Proteins/pharmacology , Zygote/drug effects
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