Lundby & Montero’s claim that diffusion limitation does not affect
(Lundby & Montero, 2015) is based essentially on two papers from the group where Lundby trained, papers they accept uncritically (Calbet et al. 2003, 2009), and the dismissal of two papers (Hogan et al. 1991; Richardson et al. 1998), which they assert are not to be believed because they contain false positive outcomes – a claim with which we disagree.
They ignore Fig. 4F in Calbet et al. (2003) where, comparing normoxia (N) to chronic hypoxia (CH), leg
is in fact directly proportional to mean leg capillary
, precisely as predicted for diffusion limitation. Those same data show higher
in normoxia than CH despite statistically identical arterial O2 concentrations (higher [Hb] in CH compensating for hypoxaemia), thereby dissociating O2 content from
. Thus, this paper actually supports the importance of diffusion limitation. Lundby & Montero reasonably question metabolism/perfusion heterogeneity rather than diffusion limitation as constraining extraction, but recent work (Vogiatzis et al. 2015) shows minimal heterogeneity, which therefore is highly unlikely to be the explanation.
The 2009 Calbet paper does not evaluate diffusion limitation, and accordingly cannot elucidate its role in limiting
– absence of evidence is not evidence of absence. It does show higher [Hb] in CH restoring O2 delivery to normoxic values despite lower leg blood flow and arterial hypoxaemia. Piiper & Scheid (1981) showed how diffusive exchange depends on the compound ratio D/(β•
) where D is diffusing capacity, β is the slope of the O2Hb dissociation curve and
is blood flow. In CH, D probably increased because of higher [Hb], β also increased with [Hb], and
was lower. Thus, it is entirely possible that D/(β•
) increased, allowing extraction to increase to restore
.
What must be understood is that O2 transport, as an integrated system involving the lungs, heart, circulation and muscles, has to be analysed as a system: all components must be measured before any can be dismissed as unimportant. Assessing only selected steps sheds no light on those com-ponents not examined. There remains no argument about the importance of the lungs, heart and circulation in transporting O2 into the muscle vasculature, but the evidence is clear that the final transport step – diffusion of O2 from the vasculature to the mitochondria – is also an important contributor to limiting
.
Call for comments
Readers are invited to give their views on this and the accompanying CrossTalk articles in this issue by submitting a brief (250 word) comment. Comments may be submitted up to 6 weeks after publication of the article, at which point the discussion will close and the CrossTalk authors will be invited to submit a ‘Last Word’. Please email your comment, including a title and a declaration of interest to jphysiol@physoc.org. Comments will be moderated and accepted comments will be published online only as ‘supporting information’ to the original debate articles once discussion has closed.
Additional information
Competing interests
The author has no conflicts of interest associated with this manuscript.
Funding
Funding was provided by NIH HL091830.
References
-
Calbet JAL, Boushel R, Radegran G, Sondergaard H, Wagner PD. Saltin B. Why is
after altitude acclimatization still reduced despite normalization of arterial O2 content. Am J Physiol Regul Integr Comp. 2003;284:R304–R316. doi: 10.1152/ajpregu.00156.2002. [DOI] [PubMed] [Google Scholar] - Calbet JAL, Radegran G, Boushel R. Saltin B. On the mechanisms that limit oxygen uptake during exercise in acute and chronic hypoxia: role of muscle mass. J Physiol. 2009;587:477–490. doi: 10.1113/jphysiol.2008.162271. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hogan MC, Bebout DE. Wagner PD. Effect of increased Hb-O2 affinity on VO2max at constant O2 delivery in dog muscle in situ. J Appl Physiol (1985) 1991;70:2656–2662. doi: 10.1152/jappl.1991.70.6.2656. [DOI] [PubMed] [Google Scholar]
-
Lundby C. Montero D. CrossTalk opposing view: Diffusion limitation of O2 from microvessels into muscle does not contribute to the limitation of
. J Physiol. 2015;593:3759–3761. doi: 10.1113/JP270550. [DOI] [PMC free article] [PubMed] [Google Scholar] - Piiper J. Scheid P. Model for capillary-alveolar equilibration with special reference to O2 uptake in hypoxia. Respir Physiol. 1981;46:193–208. doi: 10.1016/0034-5687(81)90121-3. [DOI] [PubMed] [Google Scholar]
- Richardson RS, Tagore K, Haseler L, Jordan M. Wagner PD. Increased VO2max with a right shifted Hb-O2 dissociation curve at a constant O2 delivery in dog muscle in situ. J Appl Physiol (1985) 1998;84:995–1002. doi: 10.1152/jappl.1998.84.3.995. [DOI] [PubMed] [Google Scholar]
- Vogiatzis I, Habazettl H, Louvaris Z, Andrianopoulos V, Vasilopoulou M, Nasis I, Spetsioti S, Wagner H, Zakynthinos S. Wagner PD. A method for assessing heterogeneity of blood flow and metabolism in exercising normal human muscle by near infrared spectroscopy. J Appl Physiol (1985) 2015;118:783–793. doi: 10.1152/japplphysiol.00458.2014. [DOI] [PubMed] [Google Scholar]
