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Individual differences |
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Biological: Behavioural genetics · Evolutionary psychology · Neuroanatomy · Neurochemistry · Neuroendocrinology · Neuroscience · Psychoneuroimmunology · Physiological Psychology · Psychopharmacology (Index, Outline)
Octopamine chemical structure
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Role in invertebratesEdit
Octopamine was first discovered by Italian scientist Vittorio Erspamer in 1948 in the salivary glands of the octopus and has since been found to act as neurotransmitter, neurohormone and neuromodulator in invertebrates. It is widely used in energetically demanding behaviours by all insects, crustaceans (crabs, lobsters, crayfish) and spiders. Such behaviours include flying, egg-laying and jumping.
The best understood role for octopamine is in the locust jump. Here it modulates muscle activity, making the leg muscles contract more effectively. This is at least in part due to an increase in the rate of contraction and of relaxation.
Role in vertebratesEdit
In vertebrates, octopamine also replaces norepinephrine in sympathetic neurons with chronic use of monoamine oxidase inhibitors. It is responsible for the common side effect profile of orthostatic hypotension with these agents.
In mammals, octopamine may mobilise the release of fat from adipocytes (fat cells), and this has led to its promotion on the internet as a slimming aid. However, the released fat is likely to be promptly taken up into other cells, and there is no evidence that octopamine facilitates weight loss. Octopamine may also increase blood pressure significantly when combined with other stimulants, as in some weight loss supplements.  
Use in humansEdit
In some countries octopamine is gaining increased commercial interest as an ingredient in benzylpiperazine free 'party pills'  due to the fact that in countries such as New Zealand where it is currently legal, BZP faces a probable ban before the end of 2007. It should be noted however that the structure of octopamine falls within the definition of an "amphetamine analogue" in Class C7 of the New Zealand Misuse of Drugs Act, and so would probably be considered an illegal drug if it were tested in court, although no prosecutions involving this compound have been carried out so far.
- ↑ Erspamer, V., Active substances in the posterior salivary glands of Octopoda. 2. Tyramine and octopamine (oxyoctopamine) Acta Pharmacologica et Toxicologica 4 (3-4): 224-247 1948.
- ↑ Molecular Genetic Analysis of Ethanol Intoxication in Drosophila melanogaster, Ulrike Heberlein, Fred W. Wolf, Adrian Rothenfluh and Douglas J. Guarnieri, Integrative and Comparative Biology 2004 44(4):269-274; doi:10.1093/icb/44.4.269
- ↑ Moore, M. S., Dezazzo, J., Luk, A. Y., Tully, T., Singh, C. M., and Heberlein, U. (1998) Ethanol intoxication in Drosophila: Genetic and pharmacological evidence for regulation by the cAMP pathway. Cell 93, 997-1007
- ↑ Tecott, L. H. and Heberlein, U. (1998) Y do we drink? Cell 95: 733-735
- ↑ Bar Flies: What our insect relatives can teach us about alcohol tolerance., Ruth Williams, Naked Scientist
- ↑ ‘Hangover gene’ is key to alcohol tolerance, Gaia Vince, NewScientist.com news service, 22 August 2005
- ↑ Medical News: Ephedra-Free Supplements Not Necessarily Risk-Free - in Cardiovascular, Hypertension Source: MedPage Today. URL accessed on 2007-11-30.
- ↑ Haller, CA, et al (2005) Am J Med : 118:998-1003 http://dx.doi.org/10.1016/j.amjmed.2005.02.034
- ↑ BZP Free. URL accessed on 2007-11-30.
- P.D. Evans, "Octopamine", in Comprehensive Insect Physiology, 11, 499, Oxford University Press 1985.
Adrenergic and dopaminergic agents (C01CA)
|Dobutamine • Dopamine • Epinephrine • Fenoldopam • Isoprenaline • Metaraminol • Midodrine • Norepinephrine • Octopamine • Phenylephrine|
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