More positively we could make a lot more use of domestic pets in research. If we started to treat more pets as research subjects we could really do a lot of great research.
More positively we could make a lot more use of domestic pets in research. If we started to treat more pets as research subjects we could really do a lot of great research.
There is a huge variety of mouse strains in use and under development. Basically anything you would see in a "fancy mouse" you can have as a strain.
Pets, like cats and dogs, owned by private owners, are used for studies all the time. And not just for veterinary purposes. Dogs have a wide variety of tumors, and studies on these can be used to inform research for Human oncology.
Beagles, kept in laboratory populations, are routinely used to study the cardiological safety of drugs. Such studies are rarely fatal, and dogs often have several of them during their time in the lab. They live in "colonies" of about 10 dogs each, and they look and behave just like very happy pets, even if a lot less trained. In the cases of the colonies I have been in contact with, they live in the lab for about 6 years, then they are spayed/neutered, get a complete dental and are adopted by private owners, often vets and vet students whom they already know.
Yes I know pets are used in studies, but we use pets to only a fraction of their potential. We have 10s of millions of pets and we use a few thousand at most every year. I am lamenting the waste.
A way to evaluate drug efficacy that relies less on comparisons of large groups would be a big step, because there are a lot of disorders that are probably multiple mechanisms manifesting in similar ways
Ultimately there is always going to be some trade-off between making a rigorous statement and a generalizeable one, especially because biology seems to have some pretty messy abstractions. As collecting and analyzing large amounts of data becomes more feasible, I don't see why there shouldn't be some efforts to consider genetic (or environmental) heterogeneity in animal models. Ideally I think it'd be cool to approach any given question with parallel methods that can try to address how the hypothesis holds up both in more narrow but well controlled situations, and in the "wild"
Yes we would do fewer experiments since you would need more mice per experiement, but the results of those experiements would be far more robust.
Phase I clinical trial: https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/28374166/
Phase II is in progress.
Interview with Matt Kaeberlein from the project: https://www.leafscience.org/dr-matt-kaeberlein-the-dog-aging...