PMID- 23468912 OWN - NLM STAT- MEDLINE DCOM- 20130823 LR - 20211021 IS - 1932-6203 (Electronic) IS - 1932-6203 (Linking) VI - 8 IP - 2 DP - 2013 TI - Intravenous administration of achyranthes bidentata polypeptides supports recovery from experimental ischemic stroke in vivo. PG - e57055 LID - 10.1371/journal.pone.0057055 [doi] LID - e57055 AB - BACKGROUND: Achyranthes bidentata Blume (A. bidentata) is a commonly prescribed Chinese medicinal herb. A. bidentata polypeptides (ABPP) is an active composite constituent, separated from the aqueous extract of A. bidentata. Our previous studies have found that ABPP have the neuroprotective function in vitro and in rat middle cerebral artery occlusion (MCAO) model in attenuating the brain infract area induced by focal ischemia-reperfusion. However, the ultimate goal of the stroke treatment is the restoration of behavioral function. Identifying behavioral deficits and therapeutic treatments in animal models of ischemic stroke is essential for potential translational applications. METHODOLOGY AND PRINCIPAL FINDINGS: The effect of ABPP on motor, sensory, and cognitive function in an ischemic stroke model with MCAO was investigated up to day 30. The function recovery monitored by the neurological deficit score, grip test, body asymmetry, beam-balancing task, and the Morris Water Maze. In this study, systemic administration of ABPP by i.v after MCAO decreased the neurological deficit score, ameliorated the forepaw muscle strength, and diminished the motor and sensory asymmetry on 7(th) and 30(th) day after MCAO. MCAO has been observed to cause prolonged disturbance of spatial learning and memory in rats using the MWM, and ABPP treatment could improve the spatial learning and memory function, which is impaired by MCAO in rats, on 30(th) day after MCAO. Then, the viable cells in CA1 region of hippocampus were counted by Nissl staining, and the neuronal cell death were significantly suppressed in the ABPP treated group. CONCLUSION: ABPP could improve the recovery of sensory, motor and coordination, and cognitive function in MCAO-induced ischemic rats. And this recovery had a good correlation to the less of neuronal injury in brain. FAU - Shen, Hongmei AU - Shen H AD - Key Laboratory of Neuroregeneration and Institute of Nautical Medicine, Nantong University, Nantong, China. hmshen1971@gmail.com FAU - Wu, Xinmin AU - Wu X FAU - Zhu, Yuzhong AU - Zhu Y FAU - Sun, Hualing AU - Sun H LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20130226 PL - United States TA - PLoS One JT - PloS one JID - 101285081 RN - 0 (Neuroprotective Agents) RN - 0 (Peptides) SB - IM MH - Achyranthes/*chemistry MH - Administration, Intravenous MH - Animals MH - Cerebral Infarction/drug therapy/pathology/physiopathology MH - Disease Models, Animal MH - Learning/drug effects MH - Male MH - Memory/drug effects MH - Neurons/drug effects/pathology MH - Neuroprotective Agents/administration & dosage MH - Peptides/*administration & dosage MH - Psychomotor Performance/drug effects MH - Rats MH - Stroke/*drug therapy/mortality/pathology MH - Thermosensing/drug effects PMC - PMC3582638 COIS- Competing Interests: The authors have declared that no competing interests exist. EDAT- 2013/03/08 06:00 MHDA- 2013/08/24 06:00 PMCR- 2013/02/26 CRDT- 2013/03/08 06:00 PHST- 2012/08/26 00:00 [received] PHST- 2013/01/17 00:00 [accepted] PHST- 2013/03/08 06:00 [entrez] PHST- 2013/03/08 06:00 [pubmed] PHST- 2013/08/24 06:00 [medline] PHST- 2013/02/26 00:00 [pmc-release] AID - PONE-D-12-25949 [pii] AID - 10.1371/journal.pone.0057055 [doi] PST - ppublish SO - PLoS One. 2013;8(2):e57055. doi: 10.1371/journal.pone.0057055. Epub 2013 Feb 26.