Retatrutide activates GLP-1, GIP, and glucagon receptors together. Semaglutide hits only GLP-1 while tirzepatide covers GLP-1 and GIP. The glucagon part is what sets retatrutide apart and is what likely drives any body-composition edge. It feels backwards because glucagon normally promotes protein breakdown, which is actually one of the theoretical downsides. The lean-mass sparing effect does not come from any direct muscle-protecting action; instead the glucagon piece changes how the body uses energy while in a calorie deficit. By unlocking more fuel through thermogenesis and fat breakdown, the body has less need to burn muscle. The true magnitude of this advantage over semaglutide and tirzepatide
Hi. I'm on Tirz and mostly satisfied except for the quite severe tiredness. My husband is looking to begin a glp1 peptide and I thought Reta could suit him better. I only know bits and pieces from reading around that quite a few people like Reta because it seems to hold onto lean muscle better. What exactly does Reta do differently to make that happen? When I brought it up he figured it must involve some testosterone or hgh action, but I said I didn't believe that was the case. My explanation didn't land well with him. I suggested he look into it, yet he doesn't spend much time digging online the way I do, so whatever he finds will probably be limited and possibly skewed by AI summaries.