4.7 Article Retracted Publication

被撤回的出版物: Neuroprotective effect of Liuwei Dihuang decoction on cognition deficits of diabetic encephalopathy in streptozotocin-induced diabetic rat (Retracted article. See vol. 291, 2022)

Journal

JOURNAL OF ETHNOPHARMACOLOGY
Volume 150, Issue 1, Pages 371-381

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.jep.2013.09.003

Keywords

Liuwei Dihuang decoction; Diabetic encephalopathy; Cognition deficits; Oxidative stress; Anti-apoptosis; Neuropathological changes

Funding

  1. Grant of Education Department of Shaanxi Province [12JK1019]
  2. Creative Scientific Research Projects for postgraduate student in Jiangsu General Colleges [CXLX12-0328]
  3. Natural Science Foundation of Jiangsu Province [BK2012491]
  4. National Natural Science Foundation of China [81202906]
  5. Priority Academic Program Development of Jiangsu Higher Education Institutions

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Ethnopharmacological relevance: Liuwei Dihuang decoction (LWDHD) is a well-known prescription of traditional Chinese medicine (TCM) and consists of six crude drugs including Rehmannia glutinosa Libosch. (family: Scrophulariaceae), Cornus officinalis Sieb. (family: Cornaceae), Dioscorea oppositifolia L. (family: Dioscoreaceae), Paoenia ostii (family: Paeoniaceae), Alisma orientale (G. Samuelsson) Juz (family: Alismataceae) and Poria cocos (Schw.) Wolf (family: Polyporaceae). It has been used for the treatment of Kidney-Yin deficiency syndrome in clinic in China for a long time. Recent studies found that LWDHD had a potential benefit for the treatment of diabetic complications. The aim of the present study is to investigate the neuroprotective effect of LWDHD on memory and cognition deficits in streptozotocin (STZ)-induced diabetic encephalopathy (DE) rats. Materials and methods: Adult male Sprague Dawley (SD) rats were fed with high-glucose-fat diet for 50 days and then received an intraperitoneal injection of STZ (40 mg/kg) to induce DE model. Morris water maze test was used to evaluate the memory and cognition capability of DE rats. Choline acetyltransferase (ChAT), acetylcholinesterase (AChE), Na+-K+-ATP enzyme, iNOS and GSH kits were used to determine their activities or content in hippocampus. TUNEL staining, immunohistochemistry and Congo red staining were conducted to evaluate the apoptosis, caspase-3 protein expression, insulin-like growth factors 1 (IGF-1) and brain derived neurophic factor (BDNF) expressions, as well as A beta deposition. Results: The treatment with LWDHD (1 and 2 g/kg, p.o., once daily, 30 days) could significantly reduce the escape latency time and path length, and obviously enhance the spent time in the target quadrant and platform crossings in Morris water maze test compared with model group (P<0.05, P<0.01). LWDHD could also significantly decrease the level of fasting blood glucose, increase Na+-K+-ATP enzyme and ChAT activities, enhance remarkedly GSH level while decrease significantly AChE and iNOS activities in hippocampus (P<0.05, P<0.01). Furthermore, TUNEL staining, Congo red staining and immunohistochemistry showed that LWDHD significantly improved the expressions of IGF-1 and BDNF, attenuated the neural apoptosis, overexpression of caspase-3 and A beta deposition in the hippocampus and cerebral cortex of STZ-induced DE rats (P<0.01). Conclusion: Our findings suggested that LWDHD had a neuroprotective effect on DE rats. LWDHD may be of benefit in the treatment of DE. (C) 2013 Elsevier Ireland Ltd. All rights reserved.

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