In situ cardiac perfusion reveals interspecific variation of intraventricular flow separation in reptiles

Author:

Joyce William1ORCID,Axelsson Michael2,Altimiras Jordi3,Wang Tobias1

Affiliation:

1. Department of Zoophysiology, Aarhus University, 8000 Aarhus C, Denmark

2. Department of Biological and Environmental Sciences, University of Gothenburg, Gothenburg, Sweden

3. AVIAN Behavioural Genomics and Physiology Group, IFM, Linköping University, 581 83 Linköping, Sweden

Abstract

The ventricles of non-crocodilian reptiles are incompletely divided and provide an opportunity for mixing of oxygen-poor blood and oxygen-rich blood (intracardiac shunting). However, both cardiac morphology and in vivo shunting patterns exhibit considerable interspecific variation within reptiles. In the present study, we develop an in situ double-perfused heart approach to characterise the propensity and capacity for shunting in five reptile species (turtle: Trachemys scripta, rock python: Python sebae, yellow anaconda: Eunectes notaeus, varanid lizard: Varanus exanthematicus, and bearded dragon: Pogona vitticeps). To simulate changes in vascular bed resistance, pulmonary and systemic afterloads were independently manipulated and changes in blood flow distribution amongst the central outflow tracts were monitored. As previously demonstrated in Burmese pythons, rock pythons and varanid lizards exhibited pronounced intraventricular flow separation. As pulmonary or systemic afterload was raised, flow in the respective circulation decreased. However, flow in the other circulation, where afterload was constant, remained stable. This correlates with the convergent evolution of intraventricular pressure separation and the large intraventricular muscular ridge, which compartmentalises the ventricle, in these species. Conversely, in the three other species, the pulmonary and systemic flows were strongly mutually dependent, such that the decrease in pulmonary flow in response to elevated pulmonary afterload resulted in redistribution of perfusate to the systemic circuit (and vice versa). Thus, in these species, the muscular ridge appeared labile and blood could readily transverse the intraventricular cava. We conclude that relatively minor structural differences between non-crocodilian reptiles result in the fundamental changes in cardiac function. Further, our study emphasises that functionally similar intracardiac flow separation evolved independently in lizards (varanids) and snakes (pythons) from an ancestor endowed with the capacity for large intracardiac shunts.

Funder

Danish Research Council

Swedish Research Council

Publisher

The Company of Biologists

Subject

Insect Science,Molecular Biology,Animal Science and Zoology,Aquatic Science,Physiology,Ecology, Evolution, Behavior and Systematics

Reference65 articles.

1. Cyclic carbon dioxide exchange in the turtle Pseudemys scripta;Ackerman;Physiol. Zool.,1979

2. Ventilatory compensation of the alkaline tide during digestion in the snake Boa constrictor;Andrade;J. Exp. Biol.,2004

3. Facultative thermogenesis during brooding is not the norm among pythons;Brashears;J. Comp. Physiol. A,2015

4. Pulmonary blood plasma filtration in reptiles: a ‘wet’ vertebrate lung?;Burggren;Science,1982

5. Hemodynamics and regulation of central cardiovascular shunts in reptiles;Burggren,1985

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