Another mystery was what protected the python heart from the toxic effects of huge amounts of the lipids. Further research determined that the protective substance was an enzyme, SOD (for superoxide dismutase), an antioxidant that defends cells exposed to oxygen. Eventually Dr. Riquelme returned with her family to Chile (though their departure was delayed for months by the giant earthquake in February 2010), and it was left to her colleagues in Colorado to carry out additional experiments. In one, blood plasma from bloated pythons was injected into live mice. Again, surprisingly, mouse heart cells enlarged as they would in a well-conditioned athlete.

Along the way, the Colorado team asked Dr. Secor, now at the University of Alabama in Tuscaloosa, to join in the research. He is an author of the new paper in Science. The findings leave a number of mysteries still open. What causes the organs to shrink to their fasting size? How would such findings apply to the death of human cells? And will repeated injections of the fatty acid combination safely lead to sustained increase in organ size?

Dr. Leinwand said she carried out the python research with support from federal and Colorado taxpayers and the American Heart Association. But the federal National Institutes of Health rejected her requests for direct financing, calling the relationship between reptiles and human heart disease too remote. In 2007, Dr. Leinwand became a founder of the Hiberna Corporation of Boulder to develop drugs derived from the study of exaggerated variations in animal metabolism. The company helped pay for some of the research.