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1.
Musculoskelet Surg ; 108(2): 225-230, 2024 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-38691322

RESUMO

PURPOSE: To evaluate the anxiety level to perform movements in patients after revision anterior cruciate ligament reconstruction (ACLR) combined with lateral extra-articular tenodesis (LET) compared to patients after revision ACLR without LET. METHODS: Ninety patients who underwent revision ACLR with ipsilateral bone-patellar tendon-bone autograft and with a minimum of 12 months follow-up were included in this study. Patients were divided into two groups: patients who received revision ACLR in combination with LET (revision ACLR_LET group; mean follow-up: 29.4 months, range: 12-80 months), and patients who received revision ACLR without LET (revision ACLR group; mean follow-up: 61.1 months, range: 22-192 months). All patients filled in a questionnaire about anxiety level related to physical activity and sports, the Knee injury and Osteoarthritis Outcome Score (KOOS), the International Knee Documentation Committee subjective form (IKDCsubjective), and the Tegner Activity Score. RESULTS: Patients in the revision ACLR_LET group had a significantly lower anxiety level to perform movements than patients in the revision ACLR group (p < 0.05). No significant differences were found in KOOS, IKDCsubjective, and Tegner Activity Scores. CONCLUSIONS: Patients who received LET in addition to revision ACLR have a lower anxiety level to perform movements than patients with revision ACLR alone, despite non-different subjective functional outcomes. STUDY DESIGN: Retrospective cohort study, Level of evidence: III.


Assuntos
Reconstrução do Ligamento Cruzado Anterior , Ansiedade , Reoperação , Tenodese , Humanos , Reconstrução do Ligamento Cruzado Anterior/métodos , Masculino , Feminino , Adulto , Tenodese/métodos , Ansiedade/etiologia , Adulto Jovem , Estudos Retrospectivos , Lesões do Ligamento Cruzado Anterior/cirurgia , Seguimentos , Movimento , Pessoa de Meia-Idade , Adolescente , Inquéritos e Questionários , Resultado do Tratamento
2.
Gen Comp Endocrinol ; 79(1): 114-22, 1990 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-2354773

RESUMO

The caudodorsal cells of Lymnaea and the bag cells of Aplysia are neuroendocrine cells whose peptide products have homologous functions, i.e., regulation of egg deposition. One of the Lymnaea products, calfluxin, increases cytosolic and hence mitochondrial calcium concentrations in secretory cells of the albumen gland, an exocrine organ that secretes perivitellin fluid around the egg cells during packaging; the changes can be visualized at the ultrastructural level for quantification with the pyroantimonate precipitation technique and are correlated with changes in the secretory and biosynthetic activity in the gland. Comparable studies have now been carried out with Aplysia and indicate that the bag cells of A. californica and A. brasiliana also contain a factor with calfluxin-related activity, and that the factor is not the egg-laying hormone (ELH). The bag cell factor does not affect mitochondrial calcium levels in the Lymnaea albumen gland, and synthetic calfluxin does not affect the Aplysia gland. Thus, although the bag cell and caudodorsal cell peptides have the same activity in their respective genera, the sequences have diverged sufficiently during the course of evolution to preclude cross-reactivity. Calfluxin-related activity was also detected in the atrial gland of A. californica and the atrial gland-like epithelium of A. brasiliana, two exocrine organs in the oviduct that express genes structurally related to the bag cell ELH gene. It is postulated that the active atrial gland factors may be peptides A and B.


Assuntos
Aplysia/metabolismo , Hormônios de Invertebrado/metabolismo , Neuropeptídeos/metabolismo , Sistemas Neurossecretores/metabolismo , Animais , Cálcio/metabolismo , Glândulas Exócrinas/efeitos dos fármacos , Glândulas Exócrinas/metabolismo , Glândulas Exócrinas/ultraestrutura , Lymnaea/metabolismo , Microscopia Eletrônica , Mitocôndrias/metabolismo , Neuropeptídeos/farmacologia , Sistemas Neurossecretores/ultraestrutura
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