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Tytuł pozycji:

H 2 S-stimulated bioenergetics in chicken erythrocytes and the underlying mechanism.

Tytuł:
H 2 S-stimulated bioenergetics in chicken erythrocytes and the underlying mechanism.
Autorzy:
Jin Z; Cardiovascular and Metabolic Research Unit, Laurentian University, Sudbury, Ontario, Canada.; School of Life Science, Shanxi University, Taiyuan, People's Republic of China.
Zhang Q; Cardiovascular and Metabolic Research Unit, Laurentian University, Sudbury, Ontario, Canada.; College of Environment and Resources, Shanxi University, Taiyuan, People's Republic of China.
Wondimu E; Cardiovascular and Metabolic Research Unit, Laurentian University, Sudbury, Ontario, Canada.
Verma R; Cardiovascular and Metabolic Research Unit, Laurentian University, Sudbury, Ontario, Canada.
Fu M; Cardiovascular and Metabolic Research Unit, Laurentian University, Sudbury, Ontario, Canada.; School of Human Kinetics, Laurentian University, Sudbury, Ontario, Canada.
Shuang T; Cardiovascular and Metabolic Research Unit, Laurentian University, Sudbury, Ontario, Canada.
Arif HM; Cardiovascular and Metabolic Research Unit, Laurentian University, Sudbury, Ontario, Canada.; Department of Biology, York University, Toronto, Ontario, Canada.
Wu L; Cardiovascular and Metabolic Research Unit, Laurentian University, Sudbury, Ontario, Canada.; School of Human Kinetics, Laurentian University, Sudbury, Ontario, Canada.; Health Sciences North Research Institute, Sudbury, Ontario, Canada.
Wang R; Cardiovascular and Metabolic Research Unit, Laurentian University, Sudbury, Ontario, Canada.; Department of Biology, York University, Toronto, Ontario, Canada.
Źródło:
American journal of physiology. Regulatory, integrative and comparative physiology [Am J Physiol Regul Integr Comp Physiol] 2020 Jul 01; Vol. 319 (1), pp. R69-R78. Date of Electronic Publication: 2020 May 20.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
Język:
English
Imprint Name(s):
Original Publication: Bethesda, Md. : American Physiological Society
MeSH Terms:
Energy Metabolism/*drug effects
Erythrocytes/*metabolism
Hydrogen Sulfide/*pharmacology
Adenosine Triphosphate/blood ; Animals ; Chickens ; Electron Transport/drug effects ; Erythrocytes/drug effects ; Female ; Glucose/pharmacology ; Glutamine/pharmacology ; Hypoxia/metabolism ; Mitochondria/drug effects ; Mitochondria/metabolism ; Succinic Acid/pharmacology ; Sulfurtransferases/metabolism
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Contributed Indexing:
Keywords: 3-mercaptopyruvate sulfur transferase; ATP; S-sulfhydration; avian cells; mitochondria; red blood cells
Substance Nomenclature:
0RH81L854J (Glutamine)
8L70Q75FXE (Adenosine Triphosphate)
AB6MNQ6J6L (Succinic Acid)
EC 2.8.1.- (Sulfurtransferases)
EC 2.8.1.2 (3-mercaptopyruvate sulphurtransferase)
IY9XDZ35W2 (Glucose)
YY9FVM7NSN (Hydrogen Sulfide)
Entry Date(s):
Date Created: 20200521 Date Completed: 20201005 Latest Revision: 20210702
Update Code:
20240105
PubMed Central ID:
PMC7468790
DOI:
10.1152/ajpregu.00348.2019
PMID:
32432916
Czasopismo naukowe
The production of H 2 S and its effect on bioenergetics in mammalian cells may be evolutionarily preserved. Erythrocytes of birds, but not those of mammals, have a nucleus and mitochondria. In the present study, we report the endogenous production of H 2 S in chicken erythrocytes, which was mainly catalyzed by 3-mercaptopyruvate sulfur transferase (MST). ATP content of erythrocytes was increased by MST-generated endogenous H 2 S under normoxic, but not hypoxic, conditions. NaHS, a H 2 S salt, increased ATP content under normoxic, but not hypoxic, conditions. ATP contents in the absence or presence of NaHS were eliminated by different inhibitors for mitochondrial electron transport chain in chicken erythrocytes. Succinate and glutamine, but not glucose, increased ATP content. NaHS treatment similarly increased ATP content in the presence of glucose, glutamine, or succinate, respectively. Furthermore, the expression and activity of sulfide:quinone oxidoreductase were enhanced by NaHS. The structural integrity of chicken erythrocytes was largely maintained during 2-wk NaHS treatment in vitro, whereas most of the erythrocytes without NaHS treatment were lysed. In conclusion, H 2 S may regulate cellular bioenergetics as well as cell survival of chicken erythrocytes, in which the functionality of the electron transport chain is involved. H 2 S may have different regulatory roles and mechanisms in bioenergetics of mammalian and bird cells.

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