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Progress in medicine and earthworm PDF Drucken E-Mail
Wirkstoffe - Lumbricus
Geschrieben von: http://eng.hi138.com   
Montag, den 30. Januar 2012 um 18:55 Uhr

Long used as medicine to have a long history in China. In recent years, pharmacological research and clinical application of more extensive, and have achieved encouraging results and progress.

1 Source

Earthworm (also known as worms) to participate in huge earthworm species have Pheretima Pheretima aspergilium (E. Perrier), Pheretima popular Pheretima vulgaris Chen, William Pheretima Pheretima guillelmi (Michaelsen), or blind comb Pheretima Pheretima pectinifera Michalsen dry body. The former are called "Dragon of Canton," after the three Xi said, "Shanghai to Long." pheretima caught from spring to autumn, Shanghai Dragon of the summer capture, timely cut open the abdomen, remove the internal organs and sediment washing net, dried or low temperature in dry place.

2 character identification

Pheretima: elongated article sheets, bent, edge a little volume, length 15 ~ 20 cm, width of 1 ~ 2 cm, all with links back to the purple gray brown, abdomen pale yellow brown, in addition to front and rear ends, the abdomen is cut open, internal organs have been removed or occasionally residual. mouth and anus is visible. germ band was known as "white neck", the male gonopore is also visible, often ranging from broken for the length of the segment. quality of hard and brittle, gas fishy, taste salty to be big, fat-like, not broken, no soil is preferred.

http://eng.hi138.com/?i305685_Progress-in-medicine-and-earthworm

 
Effects of Antihypertensive Protein from Pheretima on Angiotensin Ⅱ and Angiotensin Ⅱ AT_1 Receptor in Spontaneously Hypertensive Rats PDF Drucken E-Mail
Wirkstoffe - Lumbricus
Geschrieben von: http://en.cnki.com.cn   
Montag, den 30. Januar 2012 um 18:43 Uhr

OBJECTIVE:To investigate the effects of the antihypertensive protein from Pheretima on blood pressure, angiotensinⅡ and angiotensin Ⅱ AT1 receptor in spontaneously hypertensive rats (SHR).METHODS: The dynamic change of blood pressure in SHR after singel intravenous injection of antihypertensive protein from Pheretima was observed. After intervention with antihypertensive protein from earthworm for 28 d,the levels of blood pressure, angiotensinⅡ and expression of angiotensin Ⅱ AT1 receptor in SHR were detected. RESULTS: Either single intravenous injecion or multiple dosing of the antihypertensive protein from Pheretima could significantly reduce the blood pressure in SHR (P0.05); the antihypertensive protein from Pheretima could markedly lower the angiotensinⅡ level in plasma (P0.05) and slightly lower the angiotensinⅡ level in tissue of kidney but the difference was nonsignificant (P0.05).The expression of angiotensin Ⅱ AT1 receptor in kidney of SHR model increased significanlty compared the normal control (wistar rats), but decreased after the intervention of the antihypertensive protein from Pheretima.CONCLUSION: The antihypertensive protein from Pheretima has antihypertensive effect on SHR. The mechanism may be related to the reduction of angiotensinⅡ level and lowering of the expression of a angiotensin Ⅱ AT1 receptor in kidney.

http://en.cnki.com.cn/Article_en/CJFDTOTAL-ZGYA200824008.htm

 
EDRF-release and Ca+(+)-channel blockade by magnolol, an antiplatelet agent isolated from Chinese herb Magnolia officinalis, in rat thoracic aorta PDF Drucken E-Mail
Wirkstoffe - Magnolia
Geschrieben von: http://www.ncbi.nlm.nih.gov   
Donnerstag, den 26. Januar 2012 um 19:45 Uhr

Abstract

Magnolol is an antiplatelet agent isolated from Chinese herb Magnolia officinalis. It inhibited norepinephrine (NE, 3 microM)-induced phasic and tonic contractions in rat thoracic aorta. At the plateau of the NE-induced tonic contraction, addition of magnolol caused two phases (fast and slow) of relaxation. These two relaxations were concentration-dependent (10-100 micrograms/ml), and were not inhibited by indomethacin (20 microM). The fast relaxation was completely antagonized by hemoglobin (10 microM) and methylene blue (50 microM), and disappeared in de-endothelialized aorta while the slow relaxation was not affected by the above treatments. Magnolol also inhibited high potassium (60 mM)-induced, calcium-dependent (0.03 to 3 mM) contraction of rat aorta in a concentration-dependent manner. 45Ca(+)+ influx induced by high potassium or NE was markedly inhibited by magnolol. Cyclic GMP, but not PGI2, was increased by magnolol in intact, but not in de-endothelialized aorta. It is concluded that magnolol relaxed vascular smooth muscle by releasing endothelium-derived relaxing factor (EDRF) and by inhibiting calcium influx through voltage-gated calcium channels.

http://www.ncbi.nlm.nih.gov/pubmed/2172682

 
Effects of chronic treatment with honokiol in spontaneously hypertensive rats PDF Drucken E-Mail
Wirkstoffe - Magnolia
Geschrieben von: http://www.ncbi.nlm.nih.gov   
Donnerstag, den 26. Januar 2012 um 19:40 Uhr

Abstract

The present study was performed to evaluate the antihypertensive effects of honokiol in vivo in spontaneously hypertensive rats (SHR). The effects of honokiol were investigated by determination of the blood pressure, vascular reactivity, oxidative parameters, and histologic change in the aorta. Long-term administration of honokiol (400 mg/kg/d) to SHR decreased systolic blood pressure significantly. Honokiol (200, 400 mg/kg/d) enhanced the aortic relaxation in response to acetylcholine after 49-d treatment, but had no significant effects on the relaxation to sodium nitroprusside. The oral administration of honokiol significantly increased the plasma level of NO(2(-))/NO(3(-)), but decreased the level of malondialdehyde in liver of SHR compared with the control vehicle. In addition, SHR administered honokiol showed significant reductions in the elastin bands and media thickness in the aorta. These results suggest that chronic treatment with honokiol exerts an antihypertensive effect in SHR, and its vasorelaxant action and antioxidant properties may contribute to reducing the elevated blood pressure.

http://www.ncbi.nlm.nih.gov/pubmed/20190404

 
Gut modulatory, blood pressure lowering, diuretic and sedative activities of cardamom. PDF Drucken E-Mail
Wirkstoffe - Kardamon
Geschrieben von: www.ncbi.nlm.nih.gov   
Donnerstag, den 26. Januar 2012 um 17:46 Uhr

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE:

Cardamom (Elettaria cardamomum) is traditionally used in various gastrointestinal, cardiovascular and neuronal disorders.

AIM OF THE STUDY:

To rationalize cardamom use in constipation, colic, diarrhea, hypertension and as diuretic.

MATERIALS AND METHODS:

Cardamom crude extract (Ec.Cr) was studied using in vitro and in vivo techniques.

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