devil wrote:Oh, come orff it! The thalidomide problem was 50 years ago and had nothing whatsoever to do with the test-animal species. It is a teratogen in all mammalian species, including those used for drug testing. At that time, no one even thought about testing for teratogenic or mutagenic effects.
You are contradicting yourself a bit here.
Even 50 years ago they thought to do tests in a number of species.
Thalidomide was tested in mice at 50 X the dose later administered to people and it still did not induce the sedative effects it had in Humans. This goes back to my point that different chemicals behave in different ways in different species. One physician did in fact notice it had mutagenic/neurological effects which is why it was not cleared for use in the States.
Toxicological tests were all the rage in the 50s because of the emergence of chemical warfare (even earlier since Mustard Gas was used in WW I)
We know a lot more about testing than we did 50 years ago. And it's stupid to say that histologic tests 50-odd years ago would have prevented the thalidomide tragedy.
I never disputed that we know a lot more about histological tests today than we did in the 50s. It's precisely because we know so MUCH now that we can abandon animal tests altogether.
We had not developed the culture media necessary to keep cells viable.
HeLa cells which I used routinely were isolated from a patient with cervical cancer in 1951 and have been kept alive in culture media since then . . so you are entirely wrong on this point.
And shall I let you into a little secret? Mammals are always used to determine mutagenesis and teratogenesis because in vitro testing is simply not possible to term; the undesirable effects are possible at any stage of pregnancy. Please get your facts right, instead of trying to pretend you know what you are talking about, derived from myths propagated by extreme activists, as ignorant as anyone.
So far I don't think you are doing too well on the accuracy of your remarks. Your secrets had better remain that way as you would be laughed out of any modern day lab.
We have a number of isolated Human genes where mutagenic / teratogenic effect can be precisely measured and their effects on translated proteins immediately seen. These are the most powerful in vitro tests that you seem oblivious to... Once you have the gene why go back to the animal or even the wrong animal? Genomic techniques supersede all the animal tests you can think of. Because the genome is the "TARGET" for the mutagens.
I am aware of what you are talking. It may surprise you to know I took a course in industrial toxicology and epidemiology at the University of Neuchâtel, so I know more than a little of the subject.
I know of these "courses" that we offer to pharmaceutical companies. They are to "train" (brainwash) their technicians to carry out experiments according to the company ethos.
And I hold no sway by qualifications as a substitute for reasoned argument.
I know that the metabolism between species is not the same and I also know that the computer modelling can, to a large extent, predict the differences between them. This is why, for example, the results from rats can be extrapolated to humans with roughly 90% accuracy, sufficient for judging the initial posology (OK, there was one recent boo-boo!).
My ten year old knows metabolism is different according to species. The computer modelling is useless across species. I think you are getting mixed up with the computer modelling used alongside the in vitro assessments on genes (Pharmagene Labs use these) and even then they would not hazard a gung-ho figure for every drug such as you've put forward.
I have been closely involved in the toxicology of n-propyl bromide, an intermediate used in the pharma industry, notably in the synthesis of sedatives (my interest was not in the pharma application of the molecule, though). It was found to have some interesting neuropathogenic transdermal effects, found because of cutaneous tests on mice. A few cases on humans have been recorded but insufficient in number to be statistically valid for an epidemiological study. Our knowledge of the problem is derived from the animal studies, allowing us to determine ways to avoid sequelae when the substance is used industrially. Strong safety recommendations have therefore been issued. This would not have been possible without animal testing, sad though it is, but it has saved probably hundreds of people from severe neuropathy of the members, in severe cases leading to partial permanent paralysis.
Sounds like you have not been following the Health and Safety guidelines for this solvent yourself.
Again you spout a lot of rubbish. Any bacteriological test like the "Ames" test developed in the 70's and using bacteria on a Petri dish would have told you about the dangers of this chemical. Sounds like your company wastes a lot of the shareholders money if they are testing n-propyl bromide on animals. What a needlessly stupid approach.
Kuhn ("Scientific Revolutions") postulated that new approaches cannot be instigated in the sciences until the holders of the beliefs die out . . . but I think I can make you abandon vivisection for a kinder more moral, more ethical approach whilst you are still (long may it last) around. . .