TL;DR: The results suggest that divergence between the taxa in the four genera are not the result of a single historical event, and the nonconcordant divergences between allozymes and ITS sequences in Menispermum may be caused by concerted evolution in the latter or possibly longer generation time in the woody plants.
Abstract: Eastern Asian-eastern North American disjuncts in four genera were examined for allozyme divergence and sequence divergence of the internal transcribed spacers (ITS) of nuclear ribosomal DNA. The disjunct pairs of taxa include Caulophyllum robustum-C. thalictroides, Menispermum dauricum-M. canadense, Penthorum chinense-P. sedoides, and Phryma leptostachya var. asiatica-P. Ieptostachya var. leptostachya. Allozyme divergence was comparable in Caulophyllurm and Penthorum (genetic identities of 0.534 and 0.546) and was considerably higher than between pairs of taxa in Menispermum (0.273) and Phryma (0.291). Caulophyllum and Penthorum, which have the highest genetic identities at allozyme loci, also have low ITS sequence divergences (1.30 and 1.65%, respectively). Phryma, which has low isozyme identity, also has the highest ITS sequence divergence (4.46%). The two taxa of Menispermum have low ITS sequence divergence (0.93%) despite having a low identity (0.273) at allozyme loci. The results suggest that divergence between the taxa in the four genera are not the result of a single historical event. Estimated divergence times are reasonably consistent with a late Miocene disjunction for Caulophyllum and Penthorum, whereas the age of the Phryma disjunction is calculated at over 20 million years. The nonconcordant divergences between allozymes and ITS sequences in Menispermum may be caused by concerted evolution in the latter or possibly longer generation time in the woody plants. Additional molecular data are needed to clarify the situation.
TL;DR: Two new 2,4'-epoxy-8,5'-neolignans (1 and 2) were isolated from an ethyl acetate soluble portion of a hepatoprotective water decoction of Penthorum chinese and showed in vitro protective activities against acetaminophen-induced hepatocyte injury at 5 μM.
TL;DR: Wang et al. as discussed by the authors revealed a penthorum Chinese pursh tea preparation method, the method comprises the following steps: 1) taking yellow, leave and stem of penthioric pursh with water content of 40-60%, piling under the condition that the air humidity is 85-95%, and fermenting for 10-20 hours, and turning once every 5-6 hours; and 2)drying and crushing to obtain the penthorioric chenming tea.
Abstract: The invention discloses a penthorum Chinese pursh tea preparation method, the method comprises the following steps: 1)taking yellow, leave and stem of penthorum Chinese pursh with water content of 40-60%, piling under the condition that the air humidity is 85-95%, and fermenting for 10-20 hours, and turning once every 5-6 hours; and 2)drying and crushing to obtain the penthorum Chinese pursh tea. The invention also discloses the penthorum Chinese pursh tea prepared by the method. The prepared penthorum Chinese pursh tea has the advantages that the taste is pure and heavy, astringent flavor is not generated, the tea presents red bright color, the active ingredient content is high, and the prepared penthorum Chinese pursh tea has the efficacy of relieving or neutralizing the effect of alcohol and protecting liver.
TL;DR: To some extent, Penthorum Chinese Pursh is effective in inhibiting HBV replication in vitro, according to the Therapeutic Index.
Abstract: Objective: To estimate the anti-HBV effect of Penthorum Chinese Pursh. Method : Using the traditional Chinese medicine Penthorum Chinese Pursh to treat 2215 cells in vitro. Result: When the water extracts concentration was 264ug/ml, the inhibitory rate to HBeAg was 54. 79%. When the direct water extracts concentration was 57ug/ml, the inhibitory rate to HBeAg was 54. 09%. Therapeutic Index (TI) 2. Conclusion] To some extent, Penthorum Chinese Pursh is effective in inhibiting HBV replication in vitro.