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Bistortae Rhizoma (Quanshen), a dried rhizome of Polygonum bistorta L., is edited in Chinese Pharmacopiea as only one of species of Polygonum. There are many adulterants were used as Quanshen such as "Eryeliao," "Taipingyangliao" and "Daogenliao" because of its remarkable functions. Previous researches had shown that there were not significant differences among them. Therefore, it is necessary to conduct a comprehensive authentication of these herbs samples. Analyses of the microscopic features of the powders and transverse sections of herbs are the most significant measures of accreditation of the quality of traditional Chinese medicine. In this study, microscopic observation of powders of the herbs and cross‐sectional tissues were performed by using common light microscopy, polarized light microscopy and combining PCA analysis to identify Quanshen and three adulterants. We found that calcium oxalate clusters can be a good microscopic marker index to distinguish Quabshen and Eryeliao. In addition, Quanshen and the other two can be further distinguished by the characteristics of cork layer cells and vascular bundles on transverse section of the rhizome. Our results showed that the approach, microscopic features and digital characterization, is efficient, convenient, and reliable. [ABSTRACT FROM AUTHOR]

"Fangfeng" in Chinese Materia Medica refers to the dried root of Saposhnikovia divaricata (Trucz.) Schischk. The confusion regarding the species emerged centuries ago. Various medicinal plants from the family Umbelliferae have been documented under the name Fangfeng or other similar names in different areas of China. However, the efficacy and chemical profiles of these herbs can vary widely. In recent years, studies on medicinal material markets have revealed that "ChoutaiFangfeng" and "ShiFangfeng" are sold as Fangfeng. Previous studies on the differences among these herbs were not accurate; therefore, comprehensive authentication of these species is required. Investigation of the microscopic features of the transverse sections and powders of herbs is of great significance in identifying traditional Chinese medicine. This approach offers the advantages of easy operation and rapid results. In this study, microscopic observation of cross‐sectional tissues and powders of the herbs was performed using common light microscopy and polarized light microscopy, respectively, to identify Fangfeng, ChoutaiFangfeng, and ShiFangfeng. We found that phloem, clefts, and other significant tissue characteristics can be used to distinguish Fangfeng herbs. The developed method can also be applied to distinguish counterfeits of Fangfeng. Moreover, the macroscopic and microscopic characteristics of Fangfeng and its two adulterants were determined. [ABSTRACT FROM AUTHOR]

The stalks of Polygonum hydropiper L. (PHL) have been traditionally used in clinical practice for thousands of years in China to treat various inflammatory diseases. However, little research has been conducted to investigate the anti-inflammatory effects of PHL on TNBS-induced intestinal inflammation in rats. The aim of the present study was to investigate the anti-inflammatory effects and to explain the underlying mechanism of PHL on TNBS-induced intestinal inflammation in rats. PHL (125, 250, and 500 mg/kg) was given for 7 consecutive days to rats with intestinal inflammation induced by TNBS. Oral administration of an aqueous extract of a high dose of PHL (H- PHL ) significantly improved TNBS-induced symptoms such as the macroscopic score and histological examination. H- PHL treatment significantly ameliorated the activity of MPO and improved the GSH content. In addition, there was a downregulation of the TNBS-induced increase in the activity of iNOS and levels of Cox-2, TNF- α , and IL-1 β while the protein expression of NF- κ B was significantly unregulated after administration of H- PHL . The present findings suggested that H- PHL has a protective effect on experimental intestinal inflammation in rats and its anti-inflammatory effects are closely related to inhibition of NF- κ B signal pathways.