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does glp-1 affect sex drive as well?Im wondering what the ratio of GLP-1 to GIP to Glucagon for most of these twincretin and triplecretin drugs is. I am mostly interested in glucagon and GIP, with just a little glp-1.
I did a long search but it seems even pharma doesnt know.
So far I liked semaglutide the least. It's strong no doubt but energy level is kinda low, sex drive is low and the acid reflux is annoying. Tirzepatide is a lot better by far! I havent tried Retatrutide yet.
Not for me. I’ve used Semaglutide and Tirzepatide and much prefer Tirzepatide.does glp-1 affect sex drive as well?
why do you prefer the latter?Not for me. I’ve used Semaglutide and Tirzepatide and much prefer Tirzepatide.
Zero issues affecting sex drive.
This is only temporary if I get that right?any thoughts on this?
Risk of Nonarteritic Anterior Ischemic Optic Neuropathy in Patients Prescribed Semaglutide
Risk of Nonarteritic Anterior Ischemic Optic Neuropathy in Patients Prescribed Semaglutide - PubMed
This study's findings suggest an association between semaglutide and NAION. As this was an observational study, future study is required to assess causality.pubmed.ncbi.nlm.nih.gov
Nope, when it happens it's permanent. No cure, nothing at all. You are literally fucked.This is only temporary if I get that right?
@Type-IIx can we have your opinion about this.any thoughts on this?
Risk of Nonarteritic Anterior Ischemic Optic Neuropathy in Patients Prescribed Semaglutide
Risk of Nonarteritic Anterior Ischemic Optic Neuropathy in Patients Prescribed Semaglutide - PubMed
This study's findings suggest an association between semaglutide and NAION. As this was an observational study, future study is required to assess causality.pubmed.ncbi.nlm.nih.gov
Diabetes causes neuropathy and retinopathy; the association was very weak in the nondiabetes cohort (1.8%); and this was epidemiological meaning incapable of assessing causation vs. tertiary factor cause.@Type-IIx can we have your opinion about this.
Is this your first glp-1 or have you used others?Week 3 maz 3mg done. Stuff is awesome. Still feels very strong. Lost another 4 pounds. No side effects.
Semaglutid does for me. Tirzepatide is a lot better in this regards. Energy level is better on tirz as well.does glp-1 affect sex drive as well?
You don't want too much glucagon activation since it increases blood sugar and could cause muscle break down.Im interested in testing survodutide. Mostly due to its action on glucagon. I hope its a weak glp-1 receptor agonist.
Well, this is true but there are a couple more things that are of interest, especially in combination with glp-1.You don't want too much glucagon activation since it increases blood sugar and could cause muscle break down.
During fasting euglycemia, administration of glucagon caused blood glucose to rise due to increased EGP, with a delayed increase of insulin secretion. When given during experimental hyperglycemia, glucagon caused a rapid, threefold increase in insulin secretion, as well as a more gradual increase in EGP. Under both conditions, insulin clearance was decreased in response to glucagon infusion. The insulinotropic action of glucagon, which is proportional to the degree of blood glucose elevation, suggests distinct physiologic roles in the fasting and prandial states.
Interestingly, coinfusion of both glucagon and GLP-1 provides a synergistic effect on insulin secretion in humans
, which supports evidence that glucagon can increase energy expenditure
Finally, glucagon has well-documented actions for lipid metabolism (25,82), providing additional benefit for targeting hepatic steatosis. Interestingly, the ability for glucagon to promote lipid catabolism over storage may intersect with the actions of glucagon to drive ketogenesis
I don't know about other but I feel like appetite is less with tirzepatide. Overall tirz seems stronger and I feel better on it.I’m curious to understand why so many people report better appetite suppression on sema over tirz ? I was under the impression tirz being a dual agonist should have a greater impact ?
Sema hammers GLP receptors and calls it a day. Tirz hammers GIP receptors and just tickles GLP. So if you’re getting appetite suppression from the GLP action you’re going to get more of it from sema.I’m curious to understand why so many people report better appetite suppression on sema over tirz ? I was under the impression tirz being a dual agonist should have a greater impact ?