2 results match your criteria: "PortugalFaculty of MedicineUniversity of Coimbra[Affiliation]"
J Endocrinol
December 2014
Obesity CenterHospital de Santiago, EN 10, km 37, 2900-722 Setubal, PortugalFaculty of MedicineInstitutes of PhysiologyBiomedical Imaging and Life Sciences (IBILI)University of Coimbra, Polo III, Azinhaga de Santa Comba, Celas, 3000-548 Coimbra, PortugalDepartment of Surgery AUniversity Hospital of Coimbra, Rua Fonseca Pinto, 3000-075 Coimbra, PortugalFaculty of MedicineUniversity of Coimbra, Rua Larga, 3004-504 Coimbra, Portugal Obesity CenterHospital de Santiago, EN 10, km 37, 2900-722 Setubal, PortugalFaculty of MedicineInstitutes of PhysiologyBiomedical Imaging and Life Sciences (IBILI)University of Coimbra, Polo III, Azinhaga de Santa Comba, Celas, 3000-548 Coimbra, PortugalDepartment of Surgery AUniversity Hospital of Coimbra, Rua Fonseca Pinto, 3000-075 Coimbra, PortugalFaculty of MedicineUniversity of Coimbra, Rua Larga, 3004-504 Coimbra, Portugal.
Excessive or inadequate glucagon secretion promoting hepatic gluconeogenesis and glycogenolysis is believed to contribute to hyperglycemia in patients with type 2 diabetes. Currently, metabolic surgery is an accepted treatment for obese patients with type 2 diabetes and has been shown to improve glycemic control in Goto-Kakizaki (GK) rats, a lean animal model for type 2 diabetes. However, the effects of surgery on glucagon secretion are not yet well established.
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June 2014
Biology of Reproduction and Stem Cell GroupCNC-Center for Neuroscience and Cell Biology, University of Coimbra, 3004-517 Coimbra, PortugalHuman Reproduction ServiceUniversity Hospitals of Coimbra, Pr. Mota Pinto, Ed. São Jerónimo, 3000-075 Coimbra, PortugalPortuguese Institute for Blood and TransplantationCoimbra, PortugalFaculty of MedicineUniversity of Coimbra, Coimbra, PortugalDepartment of Life SciencesUniversity of Coimbra, PO Box 3046, 3001-401 Coimbra, PortugalBiology of Reproduction and Stem Cell GroupCNC-Center for Neuroscience and Cell Biology, University of Coimbra, 3004-517 Coimbra, PortugalHuman Reproduction ServiceUniversity Hospitals of Coimbra, Pr. Mota Pinto, Ed. São Jerónimo, 3000-075 Coimbra, PortugalPortuguese Institute for Blood and TransplantationCoimbra, PortugalFaculty of MedicineUniversity of Coimbra, Coimbra, PortugalDepartment of Life SciencesUniversity of Coimbra, PO Box 3046, 3001-401 Coimbra, Portugal
We have applied the mitochondria-specific superoxide fluorescent probe MitoSOX Red (MitoSOX) to detect mitochondria-specific reactive oxygen species (mROS) production in human sperm samples using flow cytometry. We show that human ejaculates are heterogeneous in terms of mROS production, with three subpopulations clearly detectable, comprising sperm that produce increasing amounts of mROS (MitoSOX-, MitoSOX+, and MitoSOX++). The sperm subpopulation producing the lowest amount of mROS represented the most functional subset of male gametes within the ejaculate, as it was correlated with the highest amount of live and non-apoptotic sperm and increased both in samples with better semen parameters and in samples processed by both density-gradient centrifugation and swim-up, both known to select for higher quality sperm.
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