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Enhanced Oxygen Utilization Efficiency With Concomitant Activation of AMPK-TBC1D1 Signaling Nexus in Cyclophilin-D Conditional Knockout Mice

We have previously reported in HEK 293 T cells and in constitutive cyclophilin-D (Cyp-D) knockout (KO) mice that Cyp-D ablation downregulates oxygen consumption (VO(2)) and triggers an adaptive response that manifest in higher exercise endurance with less VO(2). This adaptive response involves a met...

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Detalles Bibliográficos
Autores principales: Radhakrishnan, Jeejabai, Baetiong, Alvin, Gazmuri, Raúl J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8692870/
https://www.ncbi.nlm.nih.gov/pubmed/34955879
http://dx.doi.org/10.3389/fphys.2021.756659
Descripción
Sumario:We have previously reported in HEK 293 T cells and in constitutive cyclophilin-D (Cyp-D) knockout (KO) mice that Cyp-D ablation downregulates oxygen consumption (VO(2)) and triggers an adaptive response that manifest in higher exercise endurance with less VO(2). This adaptive response involves a metabolic switch toward preferential utilization of glucose via AMPK-TBC1D1 signaling nexus. We now investigated whether a similar response could be triggered in mice after acute ablation of Cyp-D using tamoxifen-induced ROSA26-Cre-mediated (i.e., conditional KO, CKO) by subjecting them to treadmill exercise involving five running sessions. At their first treadmill running session, CKO mice and controls had comparable VO(2) (208.4 ± 17.9 vs. 209.1 ± 16.8 ml/kg min(−1)), VCO(2) (183.6 ± 17.2 vs. 184.8 ± 16.9 ml/kg min(−1)), and RER (0.88 ± 0.043 vs. 0.88 ± 0.042). With subsequent sessions, CKO mice displayed more prominent reduction in VO(2) (genotype & session interaction p = 0.000) with less prominent reduction in VCO(2) resulting in significantly increased RER (genotype and session interaction p = 0.013). The increase in RER was consistent with preferential utilization of glucose as respiratory substrate (4.6 ± 0.8 vs. 4.0 ± 0.9 mg/min, p = 0.003). CKO mice also performed a significantly higher treadmill work for given VO(2) expressed as a power/VO(2) ratio (7.4 ± 0.2 × 10(−3) vs. 6.7 ± 0.2 10(−3) ratio, p = 0.025). Analysis of CKO skeletal muscle tissue after completion of five treadmill running sessions showed enhanced AMPK activation (0.669 ± 0.06 vs. 0.409 ± 0.11 pAMPK/β-tubulin ratio, p = 0.005) and TBC1D1 inactivation (0.877 ± 0.16 vs. 0.565 ± 0.09 pTBC1D1/β-tubulin ratio, p < 0.05) accompanied by increased glucose transporter-4 levels consistent with activation of the AMPK-TBC1D1 signaling nexus enabling increased glucose utilization. Taken together, our study demonstrates that like constitutive Cyp-D ablation, acute Cyp-D ablation also induces a state of increased O(2) utilization efficiency, paving the way for exploring the use of pharmacological approach to elicit the same response, which could be beneficial under O(2) limiting conditions.