Relationship Between Nitric Oxide (NO) in Follicular Fluid and Sperm Fertilization Ability
NCT03307655 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 82
Last updated 2017-10-19
Summary
Several studies indicate that Nitric Oxide (NO) plays an important role in the physiology of the reproductive system in mammals. It has been shown that NO affects sperm motility, it regulates the tyrosine phosphorylation of different sperm proteins, it enhances the sperm binding ability to the zona pellucida and it modulates the acrosome reaction.
The enzyme responsible for NO synthesis, the Nitric Oxide Synthase (NOS), has also been identified in the oocytes, cumulus and corona cells, as well as in the oviduct. For these reasons, the NOS presence at the fertilization site could be a key element to determine the success of this process. Therefore, carrying out in vitro studies to better understand NO's role in the fertilization process, especially in human sperm capacitation, could improve the outcome of the Assisted Reproductive Techniques (ARTs) due to an improvement both in the diagnosis of infertility and in the prognosis of treatment success.
This study is carried out in collaboration with the Animal Physiology Department from the Veterinary Faculty (University of Murcia, Spain) and it is funded by the European Commission under the Horizon 2020 Programme.
Conditions
- Male Infertility
Interventions
- OTHER
-
Control (fertile semen donors)
The sperm will be capacitated in the presence and absence of follicular fluid (FF). In a first set of experiments, the FF will be supplemented with L-Arginine and the NOS inhibitor L-NAME. In another set of experiments the same supplementations to the capacitation medium will be examined, but without using FF. Changes in NOS expression, protein nitrosylation, PKA activity, tyrosine phosphorylation and tyrosine nitration in sperm will be determined.
- OTHER
-
Patients (subfertile men)
The sperm will be capacitated in the presence and absence of follicular fluid (FF). In a first set of experiments, the FF will be supplemented with L-Arginine and the NOS inhibitor L-NAME. In another set of experiments the same supplementations to the capacitation medium will be examined, but without using FF. Changes in NOS expression, protein nitrosylation, PKA activity, tyrosine phosphorylation and tyrosine nitration in sperm will be determined.
Sponsors & Collaborators
-
Universidad de Murcia
collaborator OTHER -
Harvard School of Public Health (HSPH)
collaborator OTHER - collaborator OTHER
-
IVI Murcia
lead OTHER
Principal Investigators
-
Carmen Matas Parra, Professor · University of Murcia (Spain)
-
Juan Carlos Martinez Soto, MD, PhD · IVI Murcia (Spain)
-
Jorge Chavarro, MD, PhD · Harvard University
-
Florentin-Daniel Staicu, MSc · University of Murcia (Spain)
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- DIAGNOSTIC
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2017-09-21
- Primary Completion
- 2018-12-31
- Completion
- 2019-10-31
Countries
- Spain
Study Locations
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