Return to search

Mecanismos de sincronia social no ritmo circadiano de atividade durante a coabita??o em casais de saguis (Callithrix jacchus)

Submitted by Automa??o e Estat?stica (sst@bczm.ufrn.br) on 2016-06-14T20:51:44Z
No. of bitstreams: 1
ZoeliaCamilaMouraBessa_DISSERT.pdf: 3791168 bytes, checksum: e624a66aeb2a2192f56727cc91e4cb75 (MD5) / Approved for entry into archive by Arlan Eloi Leite Silva (eloihistoriador@yahoo.com.br) on 2016-06-17T20:49:25Z (GMT) No. of bitstreams: 1
ZoeliaCamilaMouraBessa_DISSERT.pdf: 3791168 bytes, checksum: e624a66aeb2a2192f56727cc91e4cb75 (MD5) / Made available in DSpace on 2016-06-17T20:49:25Z (GMT). No. of bitstreams: 1
ZoeliaCamilaMouraBessa_DISSERT.pdf: 3791168 bytes, checksum: e624a66aeb2a2192f56727cc91e4cb75 (MD5)
Previous issue date: 2015-06-08 / Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior - CAPES / Em saguis, foi observado que a sincronia entre os perfis circadianos de atividade dos animais que vivem em grupo ? mais forte entre os indiv?duos de uma mesma fam?lia do que entre fam?lias diferentes. Dentro do grupo ? mais forte entre juvenis do que entre juvenis e seus pais. No entanto, s?o desconhecidos os mecanismos envolvidos na sincronia social. Com o objetivo de investigar os mecanismos de sincroniza??o envolvidos na sincronia entre os perfis circadianos de atividade em casais de saguis, foi registrada continuamente a atividade motora por act?metros em 3 d?ades. Os casais foram submetidos a duas condi??es de ilumina??o: ciclo claro escuro CE 12:12 (CEJ I - 21 dias), e depois em claro constante (~350 lux). Em CC, os casais foram submetidos a 4 situa??es experimentais: 1. conv?vio completo (CCJ I - 24 dias), 2. remo??o de um membro do casal para outra sala com condi??es semelhantes (CCS I - 20 dias), 3. reintrodu??o do membro do casal na gaiola da 1? situa??o (CCJ II - 30 dias), e 4. remo??o do membro de cada casal para outra sala experimental (CCS II - 7 dias) para avaliar os mecanismos de sincroniza??o. Por fim, os membros do casal foram reintroduzidos na gaiola e submetidos ao ciclo CE 12:12 (CEJ II - 11 dias). Os casais entraram em livre curso na primeira condi??o em CC em conv?vio social, com per?odos id?nticos entre os membros do casal, semelhante ao observado na segunda condi??o. Nas etapas sem conv?vio social, apenas 2 f?meas entraram em livre curso na primeira etapa e 3 animais na segunda. Nas referidas condi??es, os ritmos dos animais de cada casal apresentaram diferentes per?odos end?genos. Al?m disso, nas condi??es com conv?vio social (CEJ e CCJ), os membros do casal apresentaram rela??o de fase est?vel entre si para o in?cio e fim da fase ativa, enquanto que nas etapas com separa??o entre o casal foi observada uma quebra de estabilidade nas rela??es de fase entre os perfis circadianos de atividade, com um aumento na diferen?a de ?ngulo de fase entre o casal. Ao entrar em livre curso, na transi??o entre CEJI e CCJI, todos os animais anteciparam progressivamente o in?cio e o fim da fase ativa em fase semelhante ? condi??o anterior, expressando sinal de arrastamento ao CE anterior. Enquanto que nas etapas seguintes isto foi observado em apenas 3 animais entre CCJI e CCSI, e entre CCJII e CCSII, demonstrando sinais de arrastamento ?s pistas sociais entre os membros dos casais. Por outro lado, 1 animal atrasou progressivamente entre CCJI e CCSI, 3 animais atrasaram entre CCSI e CCJII e 3 animais entre CCJII e CCSII, possivelmente por arrastamento aos animais da parte externa da col?nia. Processo semelhante foi observado em 4 animais entre CCSII e CEJII, indicando arrastamento ao CE. Na transi??o entre o CCSI e CCJII foram observados sinais de mascaramento no ritmo de uma f?mea em resposta ao macho e em outro casal no ritmo do macho em rela??o ao da f?mea. A correla??o geral e m?xima entre os perfis circadianos de atividade dos animais foi mais forte nas condi??es em conv?vio social em CE e CC do que na aus?ncia do conv?vio social em CC, evidenciando o efeito social. Os casais tiveram maiores valores para a correla??o m?xima em CE e CC juntos do que quando os perfis foram correlacionados com animais de gaiolas diferentes de mesmo ou diferente sexo. Resultados semelhantes foram observados na correla??o geral. Portanto, sugere-se que o conv?vio social favorece a uma forte sincronia entre os perfis circadianos de atividade dos casais de sagui, que envolve sincroniza??o por arrastamento e mascaramento. Por?m, estudos adicionais s?o necess?rios para avaliar o efeito das pistas sociais na sincroniza??o do ritmo circadiano da atividade entre casais de saguis na aus?ncia de pistas sociais externas a fim de confirmar esta hip?tese. / In marmosets, it was observed that the synchrony among circadian activity profiles of animals
that cohabite in family groups is stronger than those of the same sex and age of different
families. Inside the group, it is stronger between the younger ones than between them and their
parents. However, the mechanisms involved in the social synchrony are unknown. With the aim
to investigate the synchronization mechanisms involved in the synchrony between the circadian
activity profiles during cohabitation in pairs of marmosets, the motor activity was continuously
registered by the use of actmeters on three dyads. The pairs were maintained in two different
conditions of illumination: light-dark cycle LD 12:12 (LD cohabitation I ? 21 days), and
thereafter in LL (~350 lux). Under LL, the pairs were submitted to four experimental situations:
1. Cohabitation (LLJ I ? 24 days), 2. Removal of one member of the pair to another room with
similar conditions (LLS I ? 20 days), 3. Reintroduction of the separated member in the cage of
the first situation (LLJ II ? 30 days) and 4. Removal of a member from each pair to another
experimental room (LLS II ? 7 days), to evaluate the mechanisms of synchronization.
Ultimately, the members of each pair were reintroduced in the cage and were kept in LD cycle
12:12 (LDJ II ? 11 days). The rhythms of pairs free-ran in LL, with identical periods between
the members of each pair during the two stages of cohabitation. In the stages in which the
animals were separated, only the rhythms of two females free-ran in the first stage and of three
animals in the second one. In those conditions, the rhythms of animals of each pair showed
different endogenous periods. Besides, during cohabitation in LD and LL, the members of each
pair showed a stable phase relationship in the beginning of the active phase, while in the stages
in which the animals were separated it was noticed a breaking in the stability in the phase
relationships between the circadian activity profiles, with an increase in the difference in the
phase angles between them. During cohabitation, at the transition between LD and LL, all
animals showed free-running rhythms anticipating progressively the beginning and the end of
the active phase in a phase similar to the previous condition, showing signs of entrainment to
the previous LD. While in the posterior stages this was observed in only three animals between:
LLT I and LLS I, and LLT II and LLS II, evidencing signs of entrainment to social cues between
the members of each pair. On the other hand, one animal delayed progressively between LLT I
and LLS I, three animals delayed between LLS I and LLT II, and three animals between LLT
II and LLS II, perhaps by entrainment to the animals maintained outdoors in the colony. Similar
process was observed in four animals between LLS II and LDT II, indicating entrainment to
LD. In the transition between LLS I and LLT II, signs of masking was observed in the rhythm
of a female in response to the male and in another pair in the rhythm of the male in regard to
that of the female. The general and maximum correlations in the circadian activity profiles were
stronger during cohabitation in LD and LL than in the absence of social contact in LL,
evidencing the social effect. The cohabiting pairs had higher values of the maximum correlation
in LD and LL than when the profiles were correlated to animals of different cages, with same
or different sexes. Similar results were observed in the general correlation. Therefore, it is
suggested that cohabitation induces a strong synchrony between circadian activity profiles in
marmosets, which involves entrainment and masking. Nevertheless, additional studies are
necessary to evaluate the effect of social cues on the synchronization of the circadian rhythm
in pairs of marmosets in the absence of external social cues in order to confirm this hypothesis.

Identiferoai:union.ndltd.org:IBICT/oai:repositorio.ufrn.br:123456789/20727
Date08 June 2015
CreatorsBessa, Zo?lia Camila Moura
Contributors61903680425, http://lattes.cnpq.br/2667344626234863, Oda, Gisele Akemi, 11568910860, http://lattes.cnpq.br/3136915688861841, Ara?jo, John Fontenele, 22800662387, http://lattes.cnpq.br/3347815035685882, Melo, Paula Rocha de, Azevedo, Carolina Virginia Macedo de
PublisherUniversidade Federal do Rio Grande do Norte, PROGRAMA DE P?S-GRADUA??O EM PSICOBIOLOGIA, UFRN, Brasil
Source SetsIBICT Brazilian ETDs
LanguagePortuguese
Detected LanguageEnglish
Typeinfo:eu-repo/semantics/publishedVersion, info:eu-repo/semantics/masterThesis
Sourcereponame:Repositório Institucional da UFRN, instname:Universidade Federal do Rio Grande do Norte, instacron:UFRN
Rightsinfo:eu-repo/semantics/openAccess

Page generated in 0.0023 seconds