AIM: To observe the effects of polysaccharides-2b from mudan cortex of Paeonia Suffruticosa Andr on glycocylation hemoglobion(GHb),blood glucose(BG),superoxide dismutase(SOD),the content of malonaldehyde(MDA) in serum and blood rheology of diabetic rats. METHODS: Diabetic rats were induced by associating streptozotocin(STZ) with freund's adjuvant complete(CFA),and then the diabetic rats were divided randomly into five groups: model group,polysaccharides-2b lower dose group(30 mg/kg),middle dose group(60 mg/kg),high dose group(120 mg/kg),positive group.Normal group was established additionally.PSM2b was perfused into stomach in diabatic rats for 60 days.The blood glucose was measured on the 10 th,30 th and 60 th days.The rehologic indexes,GHb,SOD and MDA were measured on the 60 th days. RESULTS: Compared with model group,every administrative group of PSM2b were able to apparently reduce high blood glucose and GHb(P

This paper describes a case of maxillary first molar with 6 root canals.Preoperative CBCT helped to determine the root canal var-iation and the dental microscope assisted root canal position.The root canal retreatment for the molar was successfully completed and restored with endocrown.This case provides some reference and experience for the re-treatment of variable root canals in maxillary first molars.

Objective To establish and evaluate a rapid detection method for SARS-CoV-2 based on reverse transcriptase-recombinase aided amplification(RT-RAA)combined with the clustered regularly interspaced short palindromic repeats(CRISPR)/Cas12a system.Methods RT-RAA primers and CRISPR-derived RNA(crRNA)were designed based on the nucleocapsid(N)gene of SARS-CoV-2 from NCBI database.The detection system was optimized with magnesium acetate(MgAc)concentration,RT-RAA reaction tempera-ture and time and LbCas12a reaction temperature.The sensitivity and specificity of the method were evaluated using recombinant plas-mids(100-106 copies/μL)and other respiratory pathogens.The RT-RAA-CRISPR/Cas12a method was compared with RT-PCR by tes-ting 70 clinical samples in parallel.Results The optimized RT-RAA-CRISPR/Cas12a assay could detect SARS-CoV-2 within 50 min at 37 ℃.The limit of detection was 10 copies/μL for the fluorescence-based method and 1×102 copies/μL for the lateral flow assay.The method specifically detected SARS-CoV-2 without cross-reactivity to other respiratory pathogens.The results of testing 70 clinical samples using RT-RAA-CRISPR/Cas12a showed agreement of 100％with those of RT-PCR.Conclusion The established RT-RAA-CRISPR/Cas12a assay for SARS-CoV-2 detection is rapid,cost-effective,highly sensitive and specific.It can be performed by less experienced personnel and no expensive equipment is required,thus it may provide a new approach for rapid clinical diagnosis and large-scale on-site screening of SARS-CoV-2.