Hi all,
I'm quite new to Bluelight, but I've been impressed with what I've read here and thought this might be of interest.
I'm trained in traditional Chinese herbalism, and have recently been looking through old favorite herbs for novel uses.
This "herb" is actually the discarded shell of the cicada, Cryptotympana sp., known by the pharmaceutical name of Periostracum Cicadae, and the traditional Chinese name Chan Tui. It's classically used for many things, most notably for its anti-convulsive, anti-inflammatory, anti-pyretic, and sedative actions. It is a very mild medicinal, and thus often used for children. I've personally used it quite a bit, and find it to work quite well, if subtly, for common colds and anxiety.
At any rate, it's a very nice "herb".
What's surprising to me is that unlike most other herbs in Chinese medicine, there is a shocking lack of info in the literature about its pharmacological mechanism and components.
What I did find suggests some sort of action in which serotonin and other neurotransmitters may play a major role, thus my posting it here. The abstract of the study I found shows that the researchers, among other things, found that the herbal extract was strongly potentiated by 5-HTP. Another study found 2 N-acetyldopamine dimers to be quite active in the extract.
I guess I'm wondering if any more experienced Bluelighters can help me direct my approach to figuring out more about how this herb might work. I've got literally kilos of the stuff around in my herbal pharmacy, and was thinking I might try an extraction to see if I could isolate anything interesting.
At any rate, check out the studies below and let me know if you have any thoughts.
Studies on the anticonvulsive, sedative and hypothermic effects of Periostracum Cicadae extracts
Journul of Ethnophurmucology, 35 ( 199 I ) 83-90
Abstract:
The anticonvulsive, sedative and hypothermic effects of water and ethanol extracts of Periostracum Cicadae (PC), the cast off skin
of Cryptotympana atrutu were studied. The water-extract of whole Periostracum Cicadae (PCws) had anticonvulsive. sedative and
hypothermic effects in rats. Orally, it decreased carrageenin-induced hyperthermia. The hypothermic effect of PCws was potentiated
by S-hydroxytryptophan and antagonized by p-chlorophenylalanine. PCws enhanced the decrease in locomotor activity induced by
o-methyl-p-tyrosine or 5-hydroxytryptophan and reduced the increase in locomotor activity produced by levodopa plus benserazide
or p-chlorophenylalanine. From these results, it was concluded that the sedative and hypothermic effect of PCws may be due to an
increase in central serotonergic activity.
Antioxidant and anti-inflammatory activities of N-acetyldopamine dimers from Periostracum Cicadae
Bioorganic & Medicinal Chemistry 14 (2006) 7826–7834
Abstract
A known N-acetyldopamine dimer, (2R,3S)-2-(30,40-dihydroxyphenyl)-3-acetylamino-7-(N-acetyl-200-aminoethyl)-1,4-
benzodioxane (1) and a new N-acetyldopamine dimer, (2R,3S)-2-(30,40-dihydroxyphenyl)-3-acetylamino-7-(N-acetyl-200-aminoethylene)-
1,4-benzodioxane (2) were isolated from the methanolic extracts of Periostracum Cicadae. Compounds 1 and 2 inhibited the
Cu2+-mediated, 2,20-azobis(2-amidinopropane) hydrochloride (AAPH)-mediated, and 3-morpholinosydnonimine (SIN)-1-mediated
LDL oxidation in the thiobarbituric acid-reactive substances (TBARS) assay. The antioxidant activities of 1 and 2 were tested with
respect to other parameters, such as lag time of conjugated diene formation, relative electrophoretic mobility (REM), and apoB-100
fragmentation on copper-mediated LDL-oxidation. Compounds 1 and 2 also showed 1,1-diphenyl-2-picrylhydrasyl (DPPH) radical
scavenging activity. Compound 2 was more efficient than compound 1 at inhibiting the reactive oxygen species (ROS) generation,
nitric oxide (NO) production, and nuclear factor-jB (NF-jB) activity as well as the expression of pro-inflammatory molecules such
as inducible nitric oxide synthase (iNOS), interleukin (IL)-6, tumor necrosis factor (TNF)-a, and cyclooxygenase (COX)-2 in LPSinduced
RAW264.7 cells.
I'm quite new to Bluelight, but I've been impressed with what I've read here and thought this might be of interest.
I'm trained in traditional Chinese herbalism, and have recently been looking through old favorite herbs for novel uses.
This "herb" is actually the discarded shell of the cicada, Cryptotympana sp., known by the pharmaceutical name of Periostracum Cicadae, and the traditional Chinese name Chan Tui. It's classically used for many things, most notably for its anti-convulsive, anti-inflammatory, anti-pyretic, and sedative actions. It is a very mild medicinal, and thus often used for children. I've personally used it quite a bit, and find it to work quite well, if subtly, for common colds and anxiety.
At any rate, it's a very nice "herb".
What's surprising to me is that unlike most other herbs in Chinese medicine, there is a shocking lack of info in the literature about its pharmacological mechanism and components.
What I did find suggests some sort of action in which serotonin and other neurotransmitters may play a major role, thus my posting it here. The abstract of the study I found shows that the researchers, among other things, found that the herbal extract was strongly potentiated by 5-HTP. Another study found 2 N-acetyldopamine dimers to be quite active in the extract.
I guess I'm wondering if any more experienced Bluelighters can help me direct my approach to figuring out more about how this herb might work. I've got literally kilos of the stuff around in my herbal pharmacy, and was thinking I might try an extraction to see if I could isolate anything interesting.
At any rate, check out the studies below and let me know if you have any thoughts.
Studies on the anticonvulsive, sedative and hypothermic effects of Periostracum Cicadae extracts
Journul of Ethnophurmucology, 35 ( 199 I ) 83-90
Abstract:
The anticonvulsive, sedative and hypothermic effects of water and ethanol extracts of Periostracum Cicadae (PC), the cast off skin
of Cryptotympana atrutu were studied. The water-extract of whole Periostracum Cicadae (PCws) had anticonvulsive. sedative and
hypothermic effects in rats. Orally, it decreased carrageenin-induced hyperthermia. The hypothermic effect of PCws was potentiated
by S-hydroxytryptophan and antagonized by p-chlorophenylalanine. PCws enhanced the decrease in locomotor activity induced by
o-methyl-p-tyrosine or 5-hydroxytryptophan and reduced the increase in locomotor activity produced by levodopa plus benserazide
or p-chlorophenylalanine. From these results, it was concluded that the sedative and hypothermic effect of PCws may be due to an
increase in central serotonergic activity.
Antioxidant and anti-inflammatory activities of N-acetyldopamine dimers from Periostracum Cicadae
Bioorganic & Medicinal Chemistry 14 (2006) 7826–7834
Abstract
A known N-acetyldopamine dimer, (2R,3S)-2-(30,40-dihydroxyphenyl)-3-acetylamino-7-(N-acetyl-200-aminoethyl)-1,4-
benzodioxane (1) and a new N-acetyldopamine dimer, (2R,3S)-2-(30,40-dihydroxyphenyl)-3-acetylamino-7-(N-acetyl-200-aminoethylene)-
1,4-benzodioxane (2) were isolated from the methanolic extracts of Periostracum Cicadae. Compounds 1 and 2 inhibited the
Cu2+-mediated, 2,20-azobis(2-amidinopropane) hydrochloride (AAPH)-mediated, and 3-morpholinosydnonimine (SIN)-1-mediated
LDL oxidation in the thiobarbituric acid-reactive substances (TBARS) assay. The antioxidant activities of 1 and 2 were tested with
respect to other parameters, such as lag time of conjugated diene formation, relative electrophoretic mobility (REM), and apoB-100
fragmentation on copper-mediated LDL-oxidation. Compounds 1 and 2 also showed 1,1-diphenyl-2-picrylhydrasyl (DPPH) radical
scavenging activity. Compound 2 was more efficient than compound 1 at inhibiting the reactive oxygen species (ROS) generation,
nitric oxide (NO) production, and nuclear factor-jB (NF-jB) activity as well as the expression of pro-inflammatory molecules such
as inducible nitric oxide synthase (iNOS), interleukin (IL)-6, tumor necrosis factor (TNF)-a, and cyclooxygenase (COX)-2 in LPSinduced
RAW264.7 cells.
