imalgen
05-06-2009, 04:22 PM
Furanoeudesma-1,3-diene and curzarene
Furanoeudesma-1,3-diene, A sesqiterpene from MYRRH, is a specific agonist of opiod delta receptors
P. Dolara, C. Luceri, M. Lodovici, C. Ghelardini, S. Aiolli and M.N. Romanelli
Pharmacological Research
Volume 31, Supplement 1, 1995, Page 34
Myrrh, described in Greek medicine, Plinius and the Gospel, was
used as a perfume and as a general remedy. It is a resinous
compound from Commphorae myrrha, scrubs typical of the
Middle East. It was given to Jesus by the Magi Kings and proposed
as a drink (vinum myrratum) before crueifictinn, a potion that he
refused. We eharacterlzed ehemieaUy the components of the
hexane extract of myrrh by flash chromatography with hexane on
silica. The hexane extract had four main sesquiterpenoid
components (furanodiene, lindestrene, furanoeudesma-l,3-diene
and eurzarene, MWs ranging from 214 to 216). The mixture of
these four compounds at a dose of 50 mg/kg, increased leak
latency time in the mouse hot plate test (from 15_+0.8 s to 22_+2
s, P<0.05) and decreased the number of stretehings in the mouse
writhing test from 43+4 to 26_+2, I,_+ SE, P<0,05. These responses
were blocked by 1 mg/kg of naloxone and by the 8 specific
antagonist naltrindole (1 mg/Kg), which did not block the effect of
5 mg/kg morphine p.o. We studied the structure of curzarene and
furanoeudesma with computer molecular modelling, comparing
hem with the ~ opiod specific agonist D-Pen2D-Pen 5 (DPDPE)
and we found a good overlapping of the three steric structures. We
also characterized the binding of the sesquiterpenes of myrrh to
CNS opiod receptors with 3H-diprenorphine. Furanoeudesma was
able to displace the specific binding of diprenorphine to opioid
receptors. Myrrh contains agonists of/t oplod receptors, effective
orally, which explain its popularity in the folk medicine in the past.
There are myrrh terpene isolates available that are showing extremely strong potential. Anyone here have any experience with them?
SWIM has tried (so far) up to 75mg oral, 50mg smoked and 50mg sublingual; All provided very strong effects. Think "pleasurable sighs" and a nice "warm hug". :o
Furanoeudesma-1,3-diene, A sesqiterpene from MYRRH, is a specific agonist of opiod delta receptors
P. Dolara, C. Luceri, M. Lodovici, C. Ghelardini, S. Aiolli and M.N. Romanelli
Pharmacological Research
Volume 31, Supplement 1, 1995, Page 34
Myrrh, described in Greek medicine, Plinius and the Gospel, was
used as a perfume and as a general remedy. It is a resinous
compound from Commphorae myrrha, scrubs typical of the
Middle East. It was given to Jesus by the Magi Kings and proposed
as a drink (vinum myrratum) before crueifictinn, a potion that he
refused. We eharacterlzed ehemieaUy the components of the
hexane extract of myrrh by flash chromatography with hexane on
silica. The hexane extract had four main sesquiterpenoid
components (furanodiene, lindestrene, furanoeudesma-l,3-diene
and eurzarene, MWs ranging from 214 to 216). The mixture of
these four compounds at a dose of 50 mg/kg, increased leak
latency time in the mouse hot plate test (from 15_+0.8 s to 22_+2
s, P<0.05) and decreased the number of stretehings in the mouse
writhing test from 43+4 to 26_+2, I,_+ SE, P<0,05. These responses
were blocked by 1 mg/kg of naloxone and by the 8 specific
antagonist naltrindole (1 mg/Kg), which did not block the effect of
5 mg/kg morphine p.o. We studied the structure of curzarene and
furanoeudesma with computer molecular modelling, comparing
hem with the ~ opiod specific agonist D-Pen2D-Pen 5 (DPDPE)
and we found a good overlapping of the three steric structures. We
also characterized the binding of the sesquiterpenes of myrrh to
CNS opiod receptors with 3H-diprenorphine. Furanoeudesma was
able to displace the specific binding of diprenorphine to opioid
receptors. Myrrh contains agonists of/t oplod receptors, effective
orally, which explain its popularity in the folk medicine in the past.
There are myrrh terpene isolates available that are showing extremely strong potential. Anyone here have any experience with them?
SWIM has tried (so far) up to 75mg oral, 50mg smoked and 50mg sublingual; All provided very strong effects. Think "pleasurable sighs" and a nice "warm hug". :o