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Glucose is a pH-Dependent Motor for Sperm Beat Frequency during Early Activation

To reach the egg in the ampulla, sperm have to travel along the female genital tract, thereby being dependent on external energy sources and substances to maintain and raise the flagellar beat. The vaginal fluid is rich in lactate, whereas in the uterine fluid glucose is the predominant substrate. T...

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Autores principales: Mannowetz, Nadja, Wandernoth, Petra M., Wennemuth, Gunther
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3401232/
https://www.ncbi.nlm.nih.gov/pubmed/22911736
http://dx.doi.org/10.1371/journal.pone.0041030
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author Mannowetz, Nadja
Wandernoth, Petra M.
Wennemuth, Gunther
author_facet Mannowetz, Nadja
Wandernoth, Petra M.
Wennemuth, Gunther
author_sort Mannowetz, Nadja
collection PubMed
description To reach the egg in the ampulla, sperm have to travel along the female genital tract, thereby being dependent on external energy sources and substances to maintain and raise the flagellar beat. The vaginal fluid is rich in lactate, whereas in the uterine fluid glucose is the predominant substrate. This evokes changes in the lactate content of sperm as well as in the intracellular pH (pH(i)) since sperm possess lactate/proton co-transporters. It is well documented that glycolysis yields ATP and that HCO(3)− is a potent factor in the increase of beat frequency. We here show for the first time a pathway that connects both parts. We demonstrate a doubling of beat frequency in the mere presence of glucose. This effect can reversibly be blocked by 2-deoxy-D-glucose, dichloroacetate and aminooxyacetate, strongly suggesting that it requires both glycolysis and mitochondrial oxidation of glycolytic end products. We show that the glucose-mediated acceleration of flagellar beat and ATP production are hastened by a pH(i) ≥7.1, whereas a pH(i) ≤7.1 leaves both parameters unchanged. Since we observed a diminished rise in beat frequency in the presence of specific inhibitors against carbonic anhydrases, soluble adenylyl cyclase and protein kinase, we suggest that the glucose-mediated effect is linked to CO(2) hydration and thus the production of HCO(3)− by intracellular CA isoforms. In summary, we propose that, in sperm, glycolysis is an additional pH(i)-dependent way to produce HCO(3)−(,) thus enhancing sperm beat frequency and contributing to fertility.
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spelling pubmed-34012322012-07-30 Glucose is a pH-Dependent Motor for Sperm Beat Frequency during Early Activation Mannowetz, Nadja Wandernoth, Petra M. Wennemuth, Gunther PLoS One Research Article To reach the egg in the ampulla, sperm have to travel along the female genital tract, thereby being dependent on external energy sources and substances to maintain and raise the flagellar beat. The vaginal fluid is rich in lactate, whereas in the uterine fluid glucose is the predominant substrate. This evokes changes in the lactate content of sperm as well as in the intracellular pH (pH(i)) since sperm possess lactate/proton co-transporters. It is well documented that glycolysis yields ATP and that HCO(3)− is a potent factor in the increase of beat frequency. We here show for the first time a pathway that connects both parts. We demonstrate a doubling of beat frequency in the mere presence of glucose. This effect can reversibly be blocked by 2-deoxy-D-glucose, dichloroacetate and aminooxyacetate, strongly suggesting that it requires both glycolysis and mitochondrial oxidation of glycolytic end products. We show that the glucose-mediated acceleration of flagellar beat and ATP production are hastened by a pH(i) ≥7.1, whereas a pH(i) ≤7.1 leaves both parameters unchanged. Since we observed a diminished rise in beat frequency in the presence of specific inhibitors against carbonic anhydrases, soluble adenylyl cyclase and protein kinase, we suggest that the glucose-mediated effect is linked to CO(2) hydration and thus the production of HCO(3)− by intracellular CA isoforms. In summary, we propose that, in sperm, glycolysis is an additional pH(i)-dependent way to produce HCO(3)−(,) thus enhancing sperm beat frequency and contributing to fertility. Public Library of Science 2012-07-20 /pmc/articles/PMC3401232/ /pubmed/22911736 http://dx.doi.org/10.1371/journal.pone.0041030 Text en Mannowetz et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Mannowetz, Nadja
Wandernoth, Petra M.
Wennemuth, Gunther
Glucose is a pH-Dependent Motor for Sperm Beat Frequency during Early Activation
title Glucose is a pH-Dependent Motor for Sperm Beat Frequency during Early Activation
title_full Glucose is a pH-Dependent Motor for Sperm Beat Frequency during Early Activation
title_fullStr Glucose is a pH-Dependent Motor for Sperm Beat Frequency during Early Activation
title_full_unstemmed Glucose is a pH-Dependent Motor for Sperm Beat Frequency during Early Activation
title_short Glucose is a pH-Dependent Motor for Sperm Beat Frequency during Early Activation
title_sort glucose is a ph-dependent motor for sperm beat frequency during early activation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3401232/
https://www.ncbi.nlm.nih.gov/pubmed/22911736
http://dx.doi.org/10.1371/journal.pone.0041030
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