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1.
Zhen Ci Yan Jiu ; 49(2): 171-176, 2024 Feb 25.
Article in English, Chinese | MEDLINE | ID: mdl-38413038

ABSTRACT

OBJECTIVES: To compare the clinical effect between two acupoint regimens of moxibustion on knee osteoarthritis (KOA), and observe the influences on the serum content of interleukin 1α (IL-1α), interleukin-17A (IL-17A), tumor necrosis factor α (TNF-α), bone gla protein (BGP) and osteoprotegerin (OPG). METHODS: KOA patients were randomly divided into an observation group (40 cases, 2 cases dropped off) and a control group (40 cases, 3 cases dropped off). In the observation group, moxibustion was applied to Xiyan (EX-LE5), Dubi (ST35), Zusanli (ST36), Dazhu (BL11), Xuanzhong (GB39) and Yongquan (KI1) on the affected side. In the control group, EX-LE5, ST35 and ST36 were selected on the affected side. One session of treatment took 30 min in each group, delivered 3 times a week and the duration of treatment was 4 weeks. The scores of Western Ontario and McMaster University (WOMAC) and visual analogue scale (VAS) were observed and the serum content of IL-1α, IL-17A, TNF-α, BGP and OPG of the two groups were measured before and after treatment. RESULTS: Compared with those before treatment, the WOMAC score, VAS score and the serum content of IL-1α, IL-17A and TNF-α were decreased (P<0.05), and the content of BGP and OPG were increased (P<0.05) after treatment. Compared with the control group, the WOMAC score, VAS score and the serum content of IL-1α and TNF-α in the observation group were lower (P<0.05), and the content of BGP and OPG were higher (P<0.05). The total effective rate of the observation group was 89.5% (34/38), and that of the control group was 83.8% (31/37), with no statistically significant difference. CONCLUSIONS: Moxibustion therapy of "nourishing the kidney and benefiting the marrow" can relieve joint pain, improve joint function, reduce the level of inflammatory factors and ameliorate bone metabolic indicators. The effect of the acupoint regimen in this moxibustion therapy is better than that of the local acupoint selection.


Subject(s)
Moxibustion , Osteoarthritis, Knee , Humans , Osteoarthritis, Knee/therapy , Interleukin-17 , Bone Marrow , Tumor Necrosis Factor-alpha , Treatment Outcome , Acupuncture Points , Kidney
2.
Eur J Med Chem ; 139: 201-213, 2017 Oct 20.
Article in English | MEDLINE | ID: mdl-28802120

ABSTRACT

A series of pentacyclic triterpene 3ß-ester derivatives were designed, synthesized and evaluated as a new class of cholesteryl ester transfer protein (CETP) inhibitors for the treatment of dyslipidemia. In vitro screening assay showed that 5 out of 30 compounds displayed moderate inhibiting human CETP activity with IC50s less than 10 µM. Among them, compound 20 (IC50 = 2.3 µM) had the most potent biological activity, and effectively ameliorated plasma lipid levels of human adipose tissue specific CETP transgenic (ap2-CETPTg) mice and guinea pigs. Additional safety evaluation (no blood pressure elevation in guinea pigs) and pharmacokinetics studies indicated that the potential druggability for compound 20 which is a promising lead for development of a new class of CETP inhibitors for the treatment of dyslipidemia.


Subject(s)
Cholesterol Ester Transfer Proteins/antagonists & inhibitors , Drug Discovery , Esters/pharmacology , Triterpenes/pharmacology , Animals , Dose-Response Relationship, Drug , Esters/chemical synthesis , Esters/chemistry , Guinea Pigs , Humans , Mice , Mice, Transgenic , Molecular Structure , Structure-Activity Relationship , Triterpenes/chemical synthesis , Triterpenes/chemistry
3.
Eur J Med Chem ; 126: 143-153, 2017 Jan 27.
Article in English | MEDLINE | ID: mdl-27750148

ABSTRACT

Cholesteryl Ester Transfer Protein (CETP) is an important therapeutic target for the treatment of atherosclerotic cardiovascular disease. Our molecular modeling study revealed that pentacyclic triterpenoid compounds could mimic the protein-ligand interactions of the endogenous ligand cholesteryl ester (CE) by occupying its binding site. Alignment of the docking conformations of oleanolic acid (OA), ursolic acid (UA) and the crystal conformations of known CETP inhibitor Torcetrapib in the active site proposed the applicability of fragment-based drug design (FBDD) approaches in this study. Accordingly, a series of pentacyclic triterpenoid derivatives have been designed and synthesized as novel CETP inhibitors. The most potent compound 12e (IC50:0.28 µM) validated our strategy for molecular design. Molecular dynamics simulations illustrated that the more stable hydrogen bond interaction of the UA derivative 12e with Ser191 and stronger hydrophobic interactions with Val198, Phe463 than those of OA derivative 12b mainly led to their significantly different CETP inhibitory activity. These novel potent CETP inhibitors based on ursane-type scaffold should deserve further investigation.


Subject(s)
Cholesterol Ester Transfer Proteins/antagonists & inhibitors , Drug Design , Triterpenes/chemistry , Triterpenes/pharmacology , Catalytic Domain , Cholesterol Ester Transfer Proteins/chemistry , Cholesterol Ester Transfer Proteins/metabolism , Molecular Docking Simulation , Molecular Dynamics Simulation , Oleanolic Acid/chemistry , Triterpenes/chemical synthesis , Triterpenes/metabolism
4.
J Org Chem ; 80(19): 9620-7, 2015 Oct 02.
Article in English | MEDLINE | ID: mdl-26376091

ABSTRACT

Expeditious access to oxadiazepines via 1,5-hydride shift/cyclization of pyrrolidine- or tetrahydroisoquinoline-containing nitrones has been developed. With 1,3-dipole nitrones serving as the hydride acceptors, this transformation was promoted by a Lewis acid, providing access to structurally diverse oxadiazepines in good yields. A one-pot process for in situ nitrone formation, a 1,5-hydride shift, and ring cyclization was also realized.

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