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Interactions between depressed mothers and their infants : joint attention behaviors /Hirose, Taiko. January 1995 (has links)
Thesis (Ph. D.)--University of Washington, 1995. / Vita. Includes bibliographical references (leaves [76]-83).
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Brain galanin systems and their role in depression-like behaviour /Kuteeva, Eugenia, January 2007 (has links)
Diss. (sammanfattning) Stockholm : Karolinska institutet, 2007. / Härtill 6 uppsatser.
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Behavioral activation, cognitive therapy, and antidepressant medication in the acute treatment of major depression /Dimidjian, Sona. January 2005 (has links)
Thesis (Ph. D.)--University of Washington, 2005. / Vita. Includes bibliographical references (leaves 70-88).
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Predicting child cognitive development in low-income families /Wacharasin, Chintana. January 2001 (has links)
Thesis (Ph. D.)--University of Washington, 2001. / Vita. Includes bibliographical references (leaves [109]-122).
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Alterações dos parâmetros de comportamento de ratos tratados com peptídeo rico em prolina da serpente Bothrops jararaca, Bj-PRO-7a / Alterations of rats behavioral parameters treated with proline rich peptide of snake Bothrops jararaca, Bj-PRO-7aTurones, Larissa Córdova 16 May 2018 (has links)
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Previous issue date: 2018-05-16 / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPES / The Bj-PRO-7a, a heptapeptide isolated and identified from Bothrops jararaca (Bj) venom, evoke
potent therapeutic effects, as antihypertensive effect, natriuretic and diuretic effects, promotion of
angiogenisis and vasodilatation. The effects of heptapeptide are independent of Angiotensin
Converting Inhibitor (ACE), possibly dependent of Muscarinic Receptors subtype 1 (M1R)
activation and oxido nitric pathways. Also, the Bj-PRO-7a actions upon central nervous system
still need to be evaluated. Thus, the aims of this study were: i) to assess the effects of acute
administration of Bj-PRO-7a upon behavior; ii) to reveal mechanisms involved in the effects of Bj-
PRO-7a upon locomotion/exploration, anxiety and depression-like behaviors. For this purpose,
adult male Wistar (WT) and Spontaneous Hypertensive Rats (SHRs) (300-380 g) received i.p.
injections of Vehicle (NaCl 0.9%), Diazepam (2 mg/kg), Imipramine (15 mg/kg), Bj-PRO-7a (71,
213 or 426 nmol/kg), Pirenzepine (852 nmol/kg), α-metil-DL-tirosina (200 mg/kg) or
Chlorpromazine (2 mg/kg) and were placed in the Elevated Plus Maze (EPM), Open Field (OF)
and Forced Swimming (FS) tests. The heptapeptide promoted anxiolytic and antidepressantlike
effects and increased the locomotion/exploration. These effects of Bj-PRO-7a seem to be strongly
dependent on activation of M1R, catecholaminergic paths and dopaminergic receptors. / O Bj-PRO-7a, um heptapeptídeo isolado e identificado no veneno da Bothrops jararaca (Bj),
evoca potentes efeitos terapêuticos, tais como o efeito anti-hipertensivo, efeitos natriurético e
diurético, promoção da angiogênese e vasodilatação. Os efeitos do hepapeptídeo são independentes
da inibição sobre a Enzima Conversora de Angiotensina (ECA), possivelmente dependentes da
ativação dos Receptores Muscarínicos de Acetilcolina subtipo 1 (M1Rs) e vias do óxido nítrico.
Ademais, as ações do Bj-PRO-7a sobre o sistema nervoso central ainda precisam ser avaliadas.
Assim, os objetivos deste estudo foram: i) acessar os efeitos da administração aguda do Bj-PRO-7a
sobre o comportamento; ii) revelar os mecanismos envolvidos nos efeitos do Bj-PRO-7a sobre a
locomoção/exploração, comportamento tipo-ansiedade e depressão. Para esse propósito, ratos
machos adultos Wistar (WT) e Espontaneamente Hipertensos (SHR) (300-380 g) receberam
injeções i.p. de Veículo (NaCl 0,9%), Diazepam (2 mg/kg), Imipramina (15 mg/kg), Bj-PRO-7a
(71, 213 ou 426 nmol/kg), Pirenzepina (852 nmol/kg), α-metil-DL-tirosina (200 mg/kg) ou
Clorpromazina (2 mg/kg) e foram colocados nos testes de Labirinto em Cruz Elevado (LCE);
Campo Aberto (CA) e Nado Forçado (NF). O heptapeptídeo promoveu efeito tipo-ansiolítico e
antidepressivo e aumentou a locomoção/exploração. Esses efeitos parecem ser fortemente
dependentes da ativação dos M1Rs, vias catecolaminérgicas e receptores dopaminérgicos.
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