Cgkone
Well-known member
Orally it's basically useless less you got a whole bunchAre you saying it's basically useless? Fatburning? Stamina? Nothing?
Orally it's basically useless less you got a whole bunchAre you saying it's basically useless? Fatburning? Stamina? Nothing?
If you're a gambling man, then go for it, but it's a BIG gamble to use cardarine for the explicit purpose of preventing cancer, especially since that likely necessitates long-term use, which is a HUGE unknown, and where the issues in rats popped up.Interested in the prevention of cancer
I was hoping mike Arnold would talk more about prevention.If you're a gambling man, then go for it, but it's a BIG gamble to use cardarine for the explicit purpose of preventing cancer, especially since that likely necessitates long-term use, which is a HUGE unknown, and where the issues in rats popped up.
I don’t “100% discredit any IDEA” of it, I discredit any APPLICATION of the idea, as that’s a huge gamble to take with such a serious issue. If you’re using a drug to prevent cancer, you want the question to be “does this prevent cancer or does it not (work),” not “does this prevent cancer or does it worsen it?” You know what I mean?I was hoping mike Arnold would talk more about prevention.
We all know you 100% discredit any idea of cancer prevention.
Im hoping Arnold will explain the prevention part to me
Nobody has suggested using GW to prevent cancer.I don’t “100% discredit any IDEA” of it, I discredit any APPLICATION of the idea, as that’s a huge gamble to take with such a serious issue. If you’re using a drug to prevent cancer, you want the question to be “does this prevent cancer or does it not (work),” not “does this prevent cancer or does it worsen it?” You know what I mean?
Ok. I thought you meant you were interested in using it in an attempt to prevent cancer, which would be silly. I say we simply don’t know either way, and with such a big unknown for such a big issue, I’d stay away from it. This is especially true for people who would be using it WITH AAS and other things like that, as the biggest issue in rodents wasn’t so much CAUSING cancer as increasing the growth rate of cancer that may have been caused by other carcinogens or occurred in the rodents regardless. It’s uncharted waters, and risky, to use it with AAS, not to mention that people are using 2-2.5x more than the highest human study ever did.Nobody has suggested using GW to prevent cancer.
They are saying it more likely prevents than causes. Right?
Do you agree with that?
That makes sense. But Arnold seems to have some kind of info that says it may prevent in humans. Chados mentioned this also.Ok. I thought you meant you were interested in using it in an attempt to prevent cancer, which would be silly. I say we simply don’t know either way, and with such a big unknown for such a big issue, I’d stay away from it. This is especially true for people who would be using it WITH AAS and other things like that, as the biggest issue in rodents wasn’t so much CAUSING cancer as increasing the growth rate of cancer that may have been caused by other carcinogens or occurred in the rodents regardless. It’s uncharted waters, and risky, to use it with AAS, not to mention that people are using 2-2.5x more than the highest human study ever did.
Yeah, the in vitro (human cell studies) show promise here, but these studies have limitations, and may not pan out to a whole organism (an actual person). The authors of the studies explicitly state this. It does seem to warrant further research, but the developers have already moved on, so I don’t see that happening. It’s just a huge unknown/gamble/risk/etc.That makes sense. But Arnold seems to have some kind of info that says it may prevent in humans. Chados mentioned this also.
No. All the human studies dealing with cancer have been in vitro. There are several studies in humans using oral dosing, up to 10mg/day for 12 weeks. These studies didn’t have anything to do with cancer, and of course running 10mg for a few months isn’t going to cause cancer; it’d be INSANELY carcinogenic if that was the case. We just don’t know about longer term use (which one can argue repeated 4-week cycles can be), or even doses of 20-25mg that people like to use.So all the human studies have been in vitro?
Gotcha.No. All the human studies dealing with cancer have been in vitro. There are several studies in humans using oral dosing, up to 10mg/day for 12 weeks. These studies didn’t have anything to do with cancer, and of course running 10mg for a few months isn’t going to cause cancer; it’d be INSANELY carcinogenic if that was the case. We just don’t know about longer term use (which one can argue repeated 4-week cycles can be), or even doses of 20-25mg that people like to use.
Have you read through the TGA research compilation I posted? It discuses all the research.
It’s all good.Gotcha.
Clears it up.
I've read what you posted but sometimes I need it broken down.
Thanks!!
That makes sense. But Arnold seems to have some kind of info that says it may prevent in humans. Chados mentioned this also.
Interesting.Girroir et al., 2007 examined the effect of ligand activation of PPARδ on cell growth of two human cancer cell lines, MCF7 (breast cancer) and UACC903 (melanoma) in the presence or absence of serum using two highly specific PPARδ ligands, GW0742 or cardarine (GW501516). Culturing cells in the presence of either GW0742 or GW501516 caused up-regulation of the known PPARδ target gene angiopoietin-like protein 4 (ANGPTL4). Inhibition of cell growth was observed in both cell lines cultured in the presence of either GW0742 or GW501516, and the presence or absence of serum had little influence on this inhibition. The authors concluded that ligand activation of PPARδ inhibits the growth of both MCF7 and UACC903 cell lines and provide further evidence that PPARδ ligands are not mitogenic in human cancer cell lines.
Interesting.
There are a plethora of significant assumptions in this reasoning. This is a HUGE unknown: running cardarine long-term is UNKNOWN, running it higher than 10mg is UNKNOWN, and taking it with AAS is another huge UNKNOWN. That’s at least three major unknowns right off the bat. Are you a gambling man?Yup. Again even with long term use, if one plans on using steroids for life and takes cardarine just for the cholesterol and if cardarine would increase growth of a tumour I'm pretty sure statistically youd be in far higher risk of cardio vascular problems not taking cardarine than get cancer or faster tumour growth while taking it. In other words the benefits outweighs the possible side effects almost positively from what we've seen during the years.
Who knows though? Maybe theres more to it.
If you do use it, I’d say that 10mg is much less of a gamble than 20-25mg, so that’s good.I get some positive benefits from just 10mg
There are a plethora of significant assumptions in this reasoning. This is a HUGE unknown: running cardarine long-term is UNKNOWN, running it higher than 10mg is UNKNOWN, and taking it with AAS is another huge UNKNOWN. That’s at least three major unknowns right off the bat. Are you a gambling man?
I learned something today from this thread.......so that's the poi t of threads. Sharing of info.Why does everyone participating in this continue? Number one is there's no guaranteed answer and two is there was just a recent massive thread with the same posts repeated over and over again...just like this thread.
I don't mean the effects on cholesterol are unknown; don't be disingenuous. I mean that the effects of using more than 10mg is an unknown, as is combining it with AAS. Furthermore, we know what A SINGLE (ONE) 12 week "cycle" for 12 weeks does; we DO NOT KNOW what a 20mg/day cycle does, or what combining it with AAS does. We also don't know what happens if you run multiple cycles of it a year. Of course, running a few 12-week cycles a year is "better" than running it indefinitely for a year, but we still can't really say that the effects (if there are any) on cancer growth/development from running it multiple times in cycles not exceeding 12 weeks is the same as running it only one time ever.For cholesterol it's not unknown, its fantastic. It's been around a long time and I'm sure people have used it way beyond what I would. You don't have to run it two years if a cycle is 12 weeks
I don't mean the effects on cholesterol are unknown; don't be disingenuous. I mean that the effects of using more than 10mg is an unknown, as is combining it with AAS. Furthermore, we know what A SINGLE (ONE) 12 week "cycle" for 12 weeks does; we DO NOT KNOW what a 20mg/day cycle does, or what combining it with AAS does. We also don't know what happens if you run multiple cycles of it a year. Of course, running a few 12-week cycles a year is "better" than running it indefinitely for a year, but we still can't really say that the effects (if there are any) on cancer growth/development from running it multiple times in cycles not exceeding 12 weeks is the same as running it only one time ever.
They never setup a human trial so you dont know that it doesnt.
I believe it actually made it to phase II trials in humans before it got abandoned due to that particular rat study. But those human trials were at normal doses, I think 2.5, 5, and 10mg total.. not 10mg/kg body weight like the study that produced rampant cancer in rats.
honest answer... I'm usually more of a lurker on here than anything but I have an hour left at work and responding to this was more appealing than another hour of documentation. :dunno:
Fair enough. I'll unsubscribe from this thread...cardarine has been discussed so much lately ad nausem. Truth is no one really knows the long term effects on humans. And this is coming from someone who likes it.
There were other (lower doses) in multiple rodent studies that were deemed causes for concern, including 3 and 5 mg/kg. If you remember HED conversion, as 10mg/kg for rats isn't the same as 10mg/kg for humans, you get 33.6-56mg for a 70kg human, which isn't really that much more than the 20-25mg that lots of people use, but you're right that the human studies didn't dose higher than 10mg/day.I believe it actually made it to phase II trials in humans before it got abandoned due to that particular rat study. But those human trials were at normal doses, I think 2.5, 5, and 10mg total.. not 10mg/kg body weight like the study that produced rampant cancer in rats.