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THE ROLE OF LUTEINIZING HORMONE IN ALZHEIMER DISEASEWebber, Kate M. January 2007 (has links)
No description available.
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ÓLEOS ESSENCIAIS COMO ANESTÉSICOS PARA PEIXES: ASPECTOS BIOQUÍMICOS E MOLECULARES / ESSENTIAL OILS AS ANESTHETICS FOR FISH: BIOCHEMICAL AND MOLECULAR ASPECTSToni, Cândida 15 January 2015 (has links)
Conselho Nacional de Desenvolvimento Científico e Tecnológico / The essential oil (EOs) extracted from plants Hesperozygis ringens and Lippia alba possess
anesthetic and sedative properties and is an alternative to traditional anesthetics used in
aquaculture for ease of handling and/or reduce stress. In this sense, the study aimed to
investigate the effects of these EOs on the physiology of fish, through physiological, biochemical
and endocrine indicators. In the article 1 was determined (a) the anesthetic activity of the EOs of
H. ringens (EOHR) and L. alba (EOLA) and (b) its effects on silver catfish (Rhamdia quelen) after
induction and recovery from anesthesia. Fish were subjected to one of the following treatments
for each EO: basal group, control or anesthetized (150, 300 or 450 uL L-1 EO), evaluating the
ventilatory rate (VR) during the induction period and thereafter transferred to anesthetics-free
tanks for recovery from anesthesia. At 0, 15, 30, 60 and 240 min of recovery, samples of plasma
and gills were collected to measure metabolic indicators and ionregulatory enzymes, respectively.
In the article 2, the effects of prolonged exposure to low EOHR concentrations were studied on
silver catfish. After 6 h of exposure to 0 (control), 30 or 50 uL L-1 EOHR added to water, it was
analyzed: VR, metabolic indicators of stress in plasma, enzyme activity in liver, and expression of
pituitary hormones (growth hormone - GH, prolactin - PRL and somatolactina - SL). In the
manuscript, (a) evaluated the effectiveness of anesthesia EOLA on gilthead sea bream (Sparus
aurata) and (b) we investigated the effects of 35 uL L-1 EOLA and 2-phenoxyethanol (2-PHE) on
the stress response in gilthead sea bream undergoing persecution. After 4 h of exposure, the
plasma was sampled (for the determination of cortisol, metabolites and osmolality), brain and
pituitary (to evaluate the expression of endocrine indicators). In the article 1, anesthesia with EOs
caused changes in some parameters measured in silver catfish, but did not prevent the
restoration of most of the indicators assessed after 240 min of recovery. In the article 2, 50 uL L-1
EOHR led to an increase of glucose, lactate, protein and osmolality, as well as an increase in
metabolic enzyme activity and reduced expression of GH and SL. In the manuscript, gilthead sea
bream exposed to EOLA, stressed or not, exhibited higher levels of cortisol, glucose, lactate and
osmolality. EOLA exposure added to the stress reduced the expression levels of CRH-BP
(corticotropin releasing hormone bound to protein). PRL expression was reduced in the stressed
control group and after exposure to EOLA and 2-PHE in fish not stressed. Higher expression of
pro-opiomelanocortin (POMC) "a" and "b" were observed in fish stressed and exposed to EOLA
and 2-PHE, respectively. We conclude that: (1) the EOLA is more efficient for silver catfish that
EOHR in anesthesia concentrations; (2) for sedating the fish, it is recommended 30 uL EOHR L-1
(or less); (3) the EOLA was effective as an anesthetic for gilthead sea bream at 100-300 uL L-1,
but for 4 h exposure, the 2-PHE was more effective in preventing the stress response. / Os óleos essenciais (OEs) extraídos das plantas Hesperozygis ringens e Lippia alba possuem
propriedades anestésica e sedativa, constituindo uma alternativa aos anestésicos
tradicionalmente usados em aquicultura para facilitar o manejo e/ou reduzir o estresse. Neste
sentido, o estudo teve por objetivo investigar os efeitos desses OEs sobre a fisiologia de peixes,
através de indicadores fisiológicos, bioquímicos e endócrinos. No artigo 1 determinou-se (a) a
atividade anestésica dos OEs de H. ringens (OEHR) e L. alba (OELA) e (b) seus efeitos em
jundiá (Rhamdia quelen) depois da indução e recuperação da anestesia. Os peixes foram
submetidos a um dos seguintes tratamentos para cada OE: grupo basal, controle ou anestesiado
(150, 300 ou 450 μL L-1 OE), avaliando-se a taxa ventilatória (TV) durante o período de indução
e, posteriormente, transferidos para aquários sem anestésicos para recuperação da anestesia.
Nos tempos 0, 15, 30, 60 e 240 min de recuperação foram realizadas amostragens de plasma e
brânquias para medir indicadores metabólicos e enzimas ionorregulatórias, respectivamente. No
artigo 2, os efeitos da exposição prolongada de jundiás a baixas concentrações do OEHR foram
estudados. Após 6 h de exposição a 0 (controle), 30 ou 50 μL L-1 OEHR adicionado à água,
analisou-se: TV, indicadores metabólicos e de estresse em plasma, atividade enzimática em
fígado e expressão de hormônios hipofisários (hormônio do crescimento - GH, prolactina - PRL e
somatolactina - SL). No manuscrito (a) avaliou-se a eficácia anestésica do OELA em dourada
(Sparus aurata) e (b) investigaram-se os efeitos de 35 μL L-1 de OELA e 2-fenoxietanol (2-PHE)
sobre a resposta ao estresse em douradas submetidos à perseguição. Após 4 h de exposição,
foram amostrados plasma (para determinação dos níveis de cortisol, metabólitos e
osmolalidade), cérebro e hipófise (para avaliar a expressão de indicadores endócrinos). No artigo
1, a anestesia com os OEs provocou alterações em alguns parâmetros medidos em jundiás, mas
não impediu a restauração da maioria dos indicadores avaliados após 240 min de recuperação.
No artigo 2, 50 μL L-1 do OEHR provocou a elevação dos níveis de glicose, lactato, proteína e
osmolalidade, bem como aumento na atividade de enzimas metabólicas e redução na expressão
do GH e SL. No manuscrito, douradas expostos ao OELA, estressados ou não, exibiram maiores
níveis de cortisol, glicose, lactato e osmolalidade. A exposição ao OELA somado ao estresse
reduziu os níveis de expressão de CRH-BP (hormônio liberador de corticotrofina ligado à
proteína). A expressão de PRL foi reduzida no grupo controle estressado e após a exposição ao
OELA e 2-PHE em peixes não estressados. Maiores expressões de pro-opiomelanocortina
(POMC) a e b foram observadas em peixes estressados e expostos ao OELA e 2-PHE,
respectivamente. Conclui-se que: (1) o OELA é mais eficiente para jundiás que o OEHR em
concentrações para anestesia; (2) para sedar os peixes, recomenda-se 30 μL L-1 do OEHR (ou
menos); (3) o OELA foi eficaz como anestésico para dourada entre 100-300 μL L-1, mas para 4 h
de exposição o 2-PHE foi mais eficiente em prevenir a resposta ao estresse.
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Engineering the N-Glycosylation Pathway in Pichia Pastoris for the Expression of Glycoprotein HormonesManoharan, Simna January 2016 (has links) (PDF)
Proteins, participating in a myriad of biological function, are at the core of all cellular activities occurring within living organisms. Therapeutic proteins, hence constitute a major part of the pharmaceutical industry. The glycoprotein hormones follicle stimulating hormone (FSH), luteinizing hormone (LH), thyroid stimulating hormone (TSH) and human chorionic gonadotropin (CG) regulate various reproductive and metabolic functions in humans and hence have high therapeutic potentials. The increasing demand of recombinant proteins for therapeutic uses drives the development of better expression systems.
The methylotrophic yeast Pichia pastoris, has been termed as an industrial workhorse for heterologous protein expression. However, the N-glycosylation in yeast is of the high mannose type, resulting in a reduced serum half-life of the recombinant proteins. In the current work, we have re-engineered the Pichia N-glycosylation pathway to mimic the human type of N-glycosylation. Towards this end, we abolished the yeast native N-glycosylation and introduced enzymes from various eukaryotic sources into the system. These modifications resulted in the conversion of the yeast Man9-20GlcNAc2 glycan structure to a more human like GlcNAc2Man3GlcNAc2 form on over 70 % of the heterologous expressed proteins.
In order to demonstrate the application of these strains as efficient protein expression hosts, the glycoengineerd Pichia was used for large scale expression of the glycoprotein hormones, hCG and FSH. The purified recombinant hormones were found to have binding affinities and structure similar to that of the natural hormones. These recombinant hormones were also able to elicit over two fold responses in animal models compared to buffer controls and the activity was comparable to the natural counterparts. Thus, we report the generation of a glycoengineered Pichia pastoris, which can be considered as a serious contender for the expression of glycosylated proteins of therapeutic importance.
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