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This hypothesis was supported by femoral venous blood gas data sampled during constant exercise below and above the GET, which showed that the ODC shifts rightward at the GET. What had gone unnoticed since these original observations in 1994 was that this rightward shift begins slightly earlier, precisely when the oxygen saturation crosses the ODC inflection point. To investigate this phenomenon, we analyzed the 1994 femoral venous blood gas data obtained during cardiopulmonary exercise testing using a modern validated mechanistic biochemical model of oxygen (O\n                    <jats:sub>2<\/jats:sub>\n                    ), carbon dioxide (CO\n                    <jats:sub>2<\/jats:sub>\n                    ), and proton binding to hemoglobin (Hb). We constructed the ODC for each data point, as well as the in vivo ODC\u2014a composite curve reflecting changes in dynamic blood chemistry during exercise\u2014to assess its alignment with the GET. The model revealed that, at the in vitro ODC inflection point (36% O\n                    <jats:sub>2<\/jats:sub>\n                    Hb saturation), the amounts of CO\n                    <jats:sub>2<\/jats:sub>\n                    bound to Hb equalized with HbNH\n                    <jats:sub>3<\/jats:sub>\n                    <jats:sup>+<\/jats:sup>\n                    eventually predominating. This equilibrium apparently triggered the Bohr shift, steepening the in vivo ODC to improve O\n                    <jats:sub>2<\/jats:sub>\n                    unloading to the tissues. Shortly afterwards, the in vivo ODC reached its inflection point, matching the measured GET. Our findings support that the GET is mechanistically linked to the in vivo ODC inflection point. These results highlight the physiological relevance of determining the ODC inflection point and its alignment with HbNH\n                    <jats:sub>3<\/jats:sub>\n                    <jats:sup>+<\/jats:sup>\n                    and CO\n                    <jats:sub>2<\/jats:sub>\n                    binding as critical factors in understanding ODC shifts during cardiopulmonary exercise testing.\n                  <\/jats:p>","DOI":"10.1007\/s00424-025-03100-9","type":"journal-article","created":{"date-parts":[[2025,7,10]],"date-time":"2025-07-10T10:04:19Z","timestamp":1752141859000},"page":"1075-1087","update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":3,"title":["Oxygen dissociation curve inflection point during incremental exercise: a trigger for the Bohr effect"],"prefix":"10.1007","volume":"477","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-9462-6175","authenticated-orcid":false,"given":"Holger H.","family":"Burchert","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-2756-6728","authenticated-orcid":false,"given":"William W.","family":"Stringer","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-6751-0679","authenticated-orcid":false,"given":"Ranjan K.","family":"Dash","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2025,7,10]]},"reference":[{"key":"3100_CR1","doi-asserted-by":"publisher","unstructured":"Abdulmalik O, Ghatge MS, Musayev FN, Parikh A, Chen Q, Yang J, Nnamani I, Danso-Danquah R, Eseonu DN, Asakura T, Abraham DJ, Venitz J, Safo MK (2011) Crystallographic analysis of human hemoglobin elucidates the structural basis of the potent and dual antisickling activity of pyridyl derivatives of vanillin. 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