| Cynomel is a synthetically form of the natural
thyroid hormone 3, 5, 3' triiodothyronine, which has all the pharmacologic
activities of the natural substance. Clinically, Cynomel had been often
utilized in efforts to have treated Hypothyroidism, which is a thyroid
insufficiency, as well as other secondary symptoms such as obesity, metabolic
disorders, and fatigue. Thyroid hormones had been characteristically believed
to have been able to have exerted most of their actions through the control
of protein synthesis. When moderate amounts of Thyroid hormones had been
administered, they had been able to have increased the synthesis of RNA
and protein, which had often been followed by an increased basal metabolic
rate; as well as having stimulated the oxidative enzy;;ne systems. This,
in turn, had enhanced the release of free fatty acids from adipose tissue,
and had increased the intestinal absorption and peripheral utilization
of glucose. When higher concentrations had been apparent, this had generally
resulted in the decrease of protein synthesis, and in the increase of the
breakdown of glycogen, lipids and protein.
The Cynomel compound closely had resembled the natural thyroid hormone, Tricodide-thyronine (L-T3), and under normal circumstances, the thyroid usually had preduced two hormones, L-thyroxine (L-T4) and L4riiodine 4hyronine (L-T3). However, the latter hormone, had been much stronger and more effective of the two, and had been approximately 4 times as potent as L-T4 on a weight basis. When Cynomel had been administered orally,
it had been readily available to the body tissue with approximately 95%
of the dose being absorbed within 4 hours from the gastrointestinal tract.
The biological half-life of Cynomel had been approximately two and a half
days, with the maximal pharmacologic response having occurred within 2
or 3 days. This characteristic had also provided for an early clinical
response, as the onset of activity had usually ocatired within a few hours.
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This distinctive feature also had made it very popular amongst female athletes, due to the fact that women generally had slower metabolisms than men. Administration of Cynomel had allegedly allowed for the ridding of bodyfat, without a drastic caloric restriction. This also had perinined many athletes to have been able to have remained on high calorie diets with the added advantage of having maintained a "ripped" appearance. Athletes who had utilized Cytomel over several weeks, often had experienced a decrease in muscle mass, which had been discovered to have been avoidable or at least delayed, by the simultaneous intake of steroidal compounds, and by the consumption of a protein rich diet. Another advantage which several athletes who had administered low dosages of Cynomel had claimed tohave experienced, had been that the simultaneous intake of steroidal compounds had appeared to have become more effective. This possibly may have occurred as a result of the faster conversion of protein. Although some athletesstill had utilized the administration of Cynomel, it had not been nearly as popular as it had once appeared to have been. Spiropent, and Ephedrine (the latter is currently not available in Mexico), had emerged to have had employed the same accelerating metabolism effects, with other added advantages such as possible strength and muscle increases. The combination however, of Cynomel and Spiropent, or Ephedrine (the latter is currently not available in Mexico), had allegedly appeared to have had enormously accelerated lipolysis. BUY CYNOMEL, VISIT:
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