Specific Activity of Lactate Dehydrogenase in Muscle and Liver Tissues of Rats Exposed to Intermittent Hypobaric Hypoxia

Syarifah Dewi , Adiba Nur Ashri Ramadhani , Khoiriyyah Amalia Az-zahra , Wardaya Wardaya

BIO Integration ›› 2025, Vol. 6 ›› Issue (1) : 2

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BIO Integration ›› 2025, Vol. 6 ›› Issue (1) :2 DOI: 10.15212/bioi-2024-0074
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Specific Activity of Lactate Dehydrogenase in Muscle and Liver Tissues of Rats Exposed to Intermittent Hypobaric Hypoxia
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Abstract

As the altitude increases, the partial pressure of oxygen will decrease and cause hypobaric hypoxia conditions. During hypoxia, the anaerobic glycolysis will be activated, which is facilitated by the lactate dehydrogenase (LDH) enzyme. This study aimed to analyze the LDH-specific activity in rat muscle and liver tissue, as well as lactate and glucose levels in blood plasma after intermittent hypobaric hypoxia exposure. Twenty-five Wistar rats were divided into five groups: one control group and four hypobaric hypoxia (HH) exposure groups consisting of group 1 (1× HH), group 2 (2× HH), group 3 (3× HH), and group 4 (4× HH) with a range of 7 days between exposure. This study found that LDH-specific activity increased in muscle tissues in group 1, but then decreased in the intermittent group (groups 2–4). The change in LDH-specific activity in muscle tissues was similar to the change in lactate plasma levels. Interestingly, in liver tissues, there was a slight increase in the LDH-specific activity in group 1, and it started to increase significantly in group 2 and kept increasing in groups 3 and 4. The change in LDH-specific activity in liver tissues was similar to the change in glucose plasma level. We conclude that the LDH activity in muscle tissue contributes to lactate plasma levels, but the LDH activity in liver tissue contributes to maintaining glucose plasma after intermittent hypobaric hypoxia exposures. This finding could be implemented in individuals who experience intermittent hypoxia exposures or in various diseases with hypoxic conditions as their pathogenesis

Keywords

Enzyme activity / hypobaric hypoxia / lactate dehydrogenase / liver / muscle

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Syarifah Dewi, Adiba Nur Ashri Ramadhani, Khoiriyyah Amalia Az-zahra, Wardaya Wardaya. Specific Activity of Lactate Dehydrogenase in Muscle and Liver Tissues of Rats Exposed to Intermittent Hypobaric Hypoxia. BIO Integration, 2025, 6 (1) : 2 DOI:10.15212/bioi-2024-0074

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References

[1]

Viscor G, Torrella JR, Corral L, Ricart A, Javierre C, et al. Physiological and biological responses to short-term intermittent hypobaric hypoxia exposure: from sports and mountain medicine to new biomedical applications. Front Physiol 2018; 9: 814. [PMID: 30038574 DOI: 10.3389/fphys.2018.00814]

[2]

Rosales AM, Shute RJ, Hailes WS, Collins CW, Ruby BC, et al. Independent effects of acute normobaric hypoxia and hypobaric hypoxia on human physiology. Sci Rep 2022; 12(1): 19570. [PMID: 36379983 DOI: 10.1038/s41598-022-23698-5]

[3]

Shaw DM, Cabre G, Gant N. Hypoxic hypoxia and brain function in military aviation: basic physiology and applied perspectives. Front Physiol 2021; 12: 665821. [PMID: 34093227 DOI: 10.3389/fphys.2021.665821]

[4]

Lee P, Chandel NS, Simon MC. Cellular adaptation to hypoxia through hypoxia inducible factors and beyond. Nat Rev Mol Cell Biol 2020; 21(5): 268-83. [PMID: 32144406 DOI: 10.1038/s41580-020-0227-y]

[5]

Lee DC, Sohn HA, Park Z-Y, Oh S, Kang YK, et al. A lactate-induced response to hypoxia. Cell 2015; 161(3): 595-609. [PMID: 25892225 DOI: 10.1016/j.cell.2015.03.011]

[6]

Koziel A, Jarmuszkiewicz W. Hypoxia and aerobic metabolism adaptations of human endothelial cells. Pflügers Arch 2017; 469(5-6): 815-27. [PMID: 28176017 DOI: 10.1007/s00424-017-1935-9]

[7]

Nath B, Szabo G. Hypoxia and hypoxia inducible factors: diverse roles in liver diseases. Hepatology 2012; 55(2): 622-33. [PMID: 22120903 DOI: 10.1002/hep.25497]

[8]

Chaillou T. Skeletal muscle fiber type in hypoxia: adaptation to high-altitude exposure and under conditions of pathological hypoxia. Front Physiol 2018; 9: 1450. [PMID: 30369887 DOI: 10.3389/fphys.2018.01450]

[9]

Hara Y, Watanabe N. Changes in expression of genes related to glucose metabolism in liver and skeletal muscle of rats exposed to acute hypoxia. Heliyon 2020; 6(7): e04334. [PMID: 32642586 DOI: 10.1016/j.heliyon.2020.e04334]

[10]

Van Thienen R, Masschelein E, D’Hulst G, Thomis M, Hespel P. Twin resemblance in muscle HIF-1α responses to hypoxia and exercise. Front Physiol 2017; 7: 676. [PMID: 28149279 DOI: 10.3389/fphys.2016.00676]

[11]

Chu Q, Gu X, Zheng Q, Zhu H. Regulatory mechanism of HIF-1α and its role in liver diseases: a narrative review. Ann Transl Med 2022; 10(2): 109. [PMID: 35282052 DOI: 10.21037/atm-21-4222]

[12]

Taylor CT, Scholz CC. The effect of HIF on metabolism and immunity. Nat Rev Nephrol 2022; 18(9): 573-87. [PMID: 35726016 DOI: 10.1038/s41581-022-00587-8]

[13]

Wenger RH, Stiehl DP, Camenisch G. Integration of oxygen signaling at the consensus HRE. Sci STKE 2005; 2005(306): re12. [PMID: 16234508 DOI: 10.1126/stke.3062005re12]

[14]

Klein R, Nagy O, Tóthová C, Chovanová F. Clinical and diagnostic significance of lactate dehydrogenase and its isoenzymes in animals. Vet Med Int 2020; 2020: 5346483. [PMID: 32607139 DOI: 10.1155/2020/5346483]

[15]

Adeva-Andany M, López-Ojén M, Funcasta-Calderón R, Ameneiros-Rodríguez E, Donapetry-García C, et al. Comprehensive review on lactate metabolism in human health. Mitochondrion 2014; 17: 76-100. [PMID: 24929216 DOI: 10.1016/j.mito.2014.05.007]

[16]

Le Moine CMR, Morash AJ, McClelland GB. Changes in HIF-1α protein, pyruvate dehydrogenase phosphorylation, and activity with exercise in acute and chronic hypoxia. Am J Physiol Integr Comp Physiol 2011; 301(4): R1098-104. [PMID: 21775648 DOI: 10.1152/ajpregu.00070.2011]

[17]

Cui X-G, Han Z-T, He S-H, Wu X, Chen T-R, et al. HIF1/2α mediates hypoxia-induced LDHA expression in human pancreatic cancer cells. Oncotarget 2017; 8(15): 24840-52. [PMID: 28193910 DOI: 10.18632/oncotarget.15266]

[18]

Parlakgül G, Arruda AP, Pang S, Cagampan E, Min N, et al. Regulation of liver subcellular architecture controls metabolic homeostasis. Nature 2022; 603(7902): 736-42. [PMID: 35264794 DOI: 10.1038/s41586-022-04488-5]

[19]

Yui J, Okano S, Nishizawa H. Relationship between skeletal muscle mass and blood lactate level reduction after short squat jumps in healthy adult non-athletes. J Phys Ther Sci 2021; 33(10): 717-21. [PMID: 34658512 DOI: 10.1589/jpts.33.717]

[20]

Fresnedo O, Abad-Garcia B, Rueda Y. Tri-reagent homogenate is a suitable starting material for UHPLC-MS lipidomic analysis. Separations 2022; 9(10): 268. [DOI: 10.3390/separations9100268]

[21]

Sari D, Endardjo S, Irawati D. Blood lactate level in Wistar rats after four and twelve week intermittent aerobic training. Med J Indones 2013; 22: 141. [DOI: 10.13181/mji.v22i3.582]

[22]

Dewi S, Triatmono VR, Rasyada Ralas PR, Veraldi V, M Alfian I, et al. Increasing of LDH specific activity and PEPCK level play a role on activation of gluconeogenesis pathway in early onset pre-eeclampsia placenta. Rep Biochem Mol Biol 2022; 11(2): 320-6. [PMID: 36164619 DOI: 10.52547/rbmb.11.2.320]

[23]

Dickson LM, Buchmann EJ, Janse Van Rensburg C, Norris SA. The impact of differences in plasma glucose between glucose oxidase and hexokinase methods on estimated gestational diabetes mellitus prevalence. Sci Rep 2019; 9(1): 7238. [PMID: 31076622 DOI: 10.1038/s41598-019-43665-x]

[24]

Cassavaugh J, Lounsbury KM. Hypoxia-mediated biological control. J Cell Biochem 2011; 112(3): 735-44. [PMID: 21328446 DOI: 10.1002/jcb.22956]

[25]

Tokinoya K, Ishikura K, Yoshida Y, Ra S-G, Sugasawa T, et al. LDH isoenzyme 5 is an index of early onset muscle soreness during prolonged running. J Sports Med Phys Fitness 2020; 60(7): 1020-6. [PMID: 32253893 DOI: 10.23736/S0022-4707.20.10278-0]

[26]

Plotkin DL, Roberts MD, Haun CT, Schoenfeld BJ. Muscle fiber type transitions with exercise training: shifting perspectives. Sports 2021; 9(9): 127. [PMID: 34564332 DOI: 10.3390/sports9090127]

[27]

Clanton TL, Klawitter PF. Invited review: adaptive responses of skeletal muscle to intermittent hypoxia: the known and the unknown. J Appl Physiol 2001; 90(6): 2476-87. [PMID: 11356816 DOI: 10.1152/jappl.2001.90.6.2476]

[28]

De Smet S, van Herpt P, D’Hulst G, Van Thienen R, Van Leemputte M, et al. Physiological adaptations to hypoxic vs. normoxic training during intermittent living high. Front Physiol 2017; 8: 347. [PMID: 28620311 DOI: 10.3389/fphys.2017.00347]

[29]

Jungermann K, Kietzmann T. Oxygen: modulator of metabolic zonation and disease of the liver. Hepatology 2000; 31(2): 255-60. [PMID: 10655244 DOI: 10.1002/hep.510310201]

[30]

Minoves M, Hazane-Puch F, Moriondo G, Boutin-Paradis A, Lemarié E, et al. Differential impact of intermittent vs. sustained hypoxia on HIF-1, VEGF and proliferation of HepG2 Cells. Int J Mol Sci 2023; 24(8): 6875. [PMID: 37108039 DOI: 10.3390/ijms24086875]

[31]

Owczarek A, Gieczewska K, Jarzyna R, Jagielski AK, Kiersztan A, et al. Hypoxia increases the rate of renal gluconeogenesis via hypoxia-inducible factor-1-dependent activation of phosphoenolpyruvate carboxykinase expression. Biochimie 2020; 171-172: 31-7. [PMID: 32045650 DOI: 10.1016/j.biochi.2020.02.002]

[32]

Vora M, Pyonteck SM, Popovitchenko T, Matlack TL, Prashar A, et al. The hypoxia response pathway promotes PEP carboxykinase and gluconeogenesis in C. elegans. Nat Commun 2022; 13(1): 6168. [PMID: 36257965 DOI: 10.1038/s41467-022-33849-x]

[33]

Van Meijel RLJ, Vogel MAA, Jocken JWE, Vliex LMM, Smeets JSJ, et al. Mild intermittent hypoxia exposure induces metabolic and molecular adaptations in men with obesity. Mol Metab 2021; 53: 101287. [PMID: 34224918 DOI: 10.1016/j.molmet.2021.101287]

[34]

Zhu W, Ma Y, Guo W, Lu J, Li X, et al. Serum level of lactate dehydrogenase is associated with cardiovascular disease risk as determined by the Framingham Risk Score and arterial stiffness in a health-examined population in China. Int J Gen Med 2022; 15: 11-7. [PMID: 35018110 DOI: 10.2147/IJGM.S337517]

[35]

Mohammed SK, Taha MM, Taha EM. Cluster analysis of biochemical markers as predictor of COVID-19 severity. Baghdad Sci J 2022; 19(6(Suppl.) SE-article): 1423. [DOI: 10.21123/bsj.2022.7454]

[36]

Gupta GS. The lactate and the lactate dehydrogenase in inflammatory diseases and major risk factors in COVID-19 patients. Inflammation 2022; 45(6): 2091-123. [PMID: 35588340 DOI: 10.1007/s10753-022-01680-7]

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