Cimaterol

Cimaterol
Cimaterol is a stimulant, a fat burner, clenbuterol and similar to many and varied and some of them very important. Both are cimaterol clen and beta-agonists, and therefore the anabolic and thermogenic (Reprod Nutr Dev. 1988; 28 (1) :61-84. Domest Anim Endocrinol. October 1990, 7 (4) : 477 -84), and to stimulate the adrenal glands, elevated body temperature, increased heart rate, etc. And they imitate the "fight or flight" response is very good. Cimaterol, however, can stimulate beta-1, 2 and 3, a receiver clen only stimulates the beta 2 and 3 receivers. May this lead to an increase in the burning of fat compared with clenbuterol cimaterol. In addition, a greater proportion of brown adipose tissue is burned by means of the CIM Člen more, as far as I can tell. Cimaterol stimulates both lypolisis (fat burning: release of free fatty acids and glycerol), as well as inhibit lypogenesis (get fat: the inclusion of 14C fatty acids from [14C] glucose ) and in May is even more effective than clen, may make it more powerful fat burners. In addition, it stimulates protein synthesis and thus fat-free mass increase in May through this mechanism (Domest Anim Endocrinol. October 1990, 7 (4) :477-84) in the same time, the burning of fat. After a few weeks, however, the anabolic effects weaken in May, and one study showed an increase of weight (fat loss and muscle gain Ergo, in conjunction with the loss of fat), suspended after 14 days (J Anim Phys.-Math. January 1992, 70 (1) :115-22.). Energy metabolism is significantly increased, and CIM (Am J Physiol. December 1988, 255 (6 Pt 2): R952-60). Cimaterol also stimulates blood circulation and cause acute mobilization of nitrogen (alanine), which significantly increases the absorption of amino acids in the muscles, and mobilizes the lactic acid from the muscles (J Anim Phys.-Math. April 1998, 76 (4) :988-98.). Thus, it May not be the athletic performance (strength and possibly speed) to reduce the impact of clen (which I already wrote about the studies and references to time, I will not that I. is beyond the scope of this article). This is pure speculation on my part, and ICD in May is still some of the objectives of reducing the effects of clen and andrenergic other beta-agonists, like ephedrine can see no reason to believe he ICD (I have not read all the studies indicate that). In any case, much research that I read, and compared with those of clenbuterol Cimaterol suggests that indeed more powerful for burning fat is clen. Ok ... Now you know I have to say about Cimaterol we will see how other people have said ... Here Dan Duchaine (RIP) had to say about Cimaterol: "Until some of the new synthetic agonist beta-3 is commercially available beta-agonists of choice is always clenbuterol (although STRONGER cimaterol is available as a research product in the United States). Doug Kalman (author of "Fat Attack)," wrote about Cimaterol, and said: "While it remains to be tested on humans, animal studies found Cimaterol which is more powerful than beta-agonists, clenbuterol, the protein to promote the conservation and sediment, but also showed a strong anti-catabolic properties in the case of cancer or burns. " So yes, things are not only more fat burner, it is anti-catabolic. Seems promising, no? Unfortunately, it regulates beta receptors and clen (J Anim Phys.-Math. January 1992, 70 (1) :115-22.) Thus, for 3 weeks to 1 week type of schedule in May and also appropriate add Ketotifen when, after 3 weeks (and will not cimaterol And cimaterol 4 weeks, every 4 weeks, which must be added to the MGS 2-3 Ketotifen in every night before bed). You can also use 50mg of Banadryl rather than Ketotifen in the same way. As with any new drug, precautions must be taken with this thing. Dose of 0.15 mg / kg administered subcutaneously at a standard dose in human studies, I try to ease the dose of me, but I prefer tablets (also available). This is the part of any form of dangerous doses. Cimaterol, LD50: 1.973 mg / kg (males) and 1745 mg / kg (female)