Phentermine Online blog
Phentermine is used as an appetite suppressant in conjunction with an overall diet.
Phentermine has been used in the USA to treat obesity sinc, at least 1961 and was widely used after 1992 in combinatio. with fenfIuramine_ A swdy in 1997 suggested that thi combination could be associated with hean-valve diseas similar to that seen in the carcinoid syndrome or in patients who had taken ergotamine, as well as with pulmo hypertension, previously descn”bed.’ It was suggested that these findings, were’ due to an increase in circulating! serotonin. Subsequently, the US Food and Drug! Administration found heart-valve lesions among patients I taking a fenfluramine without phentermine. ‘ Given the paucity of data on’ phentermine’s actions, we detennined whether phentermine could modify the metabolism of other monoamines besides the norepinephrine released from sympathetic neurons. In rats, phentermine, like d-amphetamine, releases dopamine into: brain synapses! We tested the ability of a low dose (15 mg’ by mouth) to affect plasma dopamine in human beings.
Nine young, non-obese male volunteers gave blood, just ‘before, I and 1, 2, or 4 h after receiving the drug. Plasma dopamine concentrations, assayed by radioimmunoassay’, rose with’ phentermine’ (p<0′05; ANOVA;,Wllcoxon’s test); however a’ greater increase was noted in serotin levelswithin the blood platelets as assayed by EIlSA and confirmed by high performance liquid ‘chromatography, (r=0-496; p<O-OOI). The increase in’ platelet stonin’ could reflect increased release of serotonm from” ‘enterochromaffin cells, or inhI”bitionof its met:iboIism by monoamine oxidase (MAO)_ That the increase resuItedfrom MAO inhibition and not from increased serotonin release was shown by the finding that plasma seroto concentionfell slightly.
Phentermine Online blog
That phenterri1ine inhI”bitstheMAO which qJtabolises serotonin was well known in the early 1970s,’ but apparently this in(onnation never made its way onto the drug’s label. There is evidence that free plasma serotonin can damage vascular tissue’ and that its concentration is normally kept low by the action of the tWo high-capacity’ systems that remove it from the circulation-uptake into platelets and MAO. If the fenfluramine and phentermine regimen did produce pulmonary hypertension and cardiac valve lesions then they might have been obviated had the phetermine label within the US mentioned that the drug is an MAO inhI”bitor. Such a mention would also’ warn physicians against combining phentermine with fIuoxetine, fIenf1uramine, or other SSRIs.
Srudies supported in part by grants for the Natioual InstitUtes of Health (NCRR=MO-I-RROOO88) and CcntQ” for Brain Sciences and Metabolism Charit2ble TrusL We thank Jeff Breu for acd1ent technic:a1assistance. and Panicle Ohagen and Robert Parker for advice and help with the statistic:a1analyses. Abenhaim L, Moricle Y, Brcnot F, et al. Appetite-suppressant drugs and the risk of primary pulmoDal)’ hypertension. N Engl J Md 1996; 335: 609-615. 2 Balcioglu A, Wunman RJ. Effects of phentennine on saiaw dopamine and serotonin release in conscious rats: in vivo miaodialysis stUdy. InrJ Obesit;y1998; 22: 325-328. 3 Manz B, Lorey M, Heyn S, et al. New radioimmunoassays for epinephrine and norepinephrine in plasma and urine as well as mecanephrines Uld normecanephrines in urine. arI’lAbor Mtdizin 1990; 5: 245-263. 4 MaUer Nielsen I, Dubnick B. Pharmacology of chJorphentc:rmine. In: Amphetamines and Related Compounds (E Costa, S Garattini, cds) Raven Press, NY, 1970, pp 673 .Tags:Phentermine Online blog