ABSTRACT
As raízes de algodäozinho-do-campo - Cochlospermum regium (Mart. et Schr.) Pilger na forma de droga fragmentada e pulverizada, foram caracterizadas de modo a fornecer descriçöes farmacognósticas para sua identificaçäo. Fotomicrografias e figuras acompanharam as descriçöes.
Subject(s)
Ethnobotany , Pharmacognosy , Plants, Medicinal , Plant Roots/metabolism , Plant Roots/chemistry , Plant Roots/therapeutic useABSTRACT
Extract of Nelumbo nucifera rhizome (RNN) was used as anti-diarrheal agent to combat the diarrhea in experimental rats. The RNN extract in graded doses (100, 200, 400 and 600 mg/kg body wt.) reduced not only the frequency of defecation, wetness of fecal dropping and PGE2 induced enteropooling but also the propulsive movements of charcoal meal significantly.
Subject(s)
Administration, Oral , Animals , Antidiarrheals/therapeutic use , Atropine/therapeutic use , Cathartics/therapeutic use , Cecum/drug effects , Diarrhea/drug therapy , Dinoprostone/pharmacology , Female , Gastrointestinal Motility/drug effects , Intestinal Mucosa/drug effects , Intestinal Secretions/drug effects , Male , Parasympatholytics/therapeutic use , Phytotherapy , Plant Extracts/administration & dosage , Plant Roots/therapeutic use , Plants, Medicinal/therapeutic use , Pylorus/drug effects , Rats , Rats, Long-Evans , Tragacanth/therapeutic useABSTRACT
Panax ginseng roots have long been used as a medicinal herb in oriental countries. We have investigated anti-proliferative effects of lipid soluble Panax ginseng components on human renal cancer cell lines. Petroleum ether extract of Panax ginseng roots (GX-PE) or its partially purified preparation (7:3 GX) was added to cultures of three human renal cell carcinoma (RCC) cell lines, A498, Caki-1, and CURC II. Proliferation of RCC cells was estimated by a [3H]thymidine incorporation assay and cell cycle distribution was analyzed by flow cytometry. GX-PE, 7:3 GX, panaxydol and panaxynol inhibited proliferation of all three RCC cell lines in a dose dependent manner in vitro with an order of potency, 7:3 GX > panaxydol > panaxynol = GX-PE. Additive effect of interleukin 4 was also demonstrated, most prominently in Caki-1 which responded poorly to GX-PE alone. Analysis of cell cycle in CURC II and Caki-1 treated with GX-PE demonstrated increase in G1 phase population and corresponding decrease in S phase population. The present study demonstrated that proliferation of human RCC cell lines were inhibited by lipid soluble components of Panax ginseng roots by blocking cell cycle progression at G1 to S phase transition.