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The bioactive alkaloids identified from Cortex Phellodendri ameliorate benign prostatic hyperplasia via LOX-5/COX-2 pathways.
Wang, Siqi; Lee, David Yue-Wei; Shang, Ying; Liao, Jun; Cao, Xiaotong; Xie, Linlin; Zhang, Teng; Liu, Jing; Dai, Ronghua.
Affiliation
  • Wang S; School of Pharmacy, Shenyang Pharmaceutical University, Wenhua Road 103, Shenyang, Liaoning 110016, China.
  • Lee DY; Mailman Research Center, McLean Hospital, Harvard Medical School, Boston, MA, United States.
  • Shang Y; School of Pharmacy, Shenyang Pharmaceutical University, Wenhua Road 103, Shenyang, Liaoning 110016, China.
  • Liao J; School of Pharmacy, Shenyang Pharmaceutical University, Wenhua Road 103, Shenyang, Liaoning 110016, China.
  • Cao X; School of Pharmacy, Shenyang Pharmaceutical University, Wenhua Road 103, Shenyang, Liaoning 110016, China.
  • Xie L; School of Pharmacy, Shenyang Pharmaceutical University, Wenhua Road 103, Shenyang, Liaoning 110016, China.
  • Zhang T; School of Pharmacy, Shenyang Pharmaceutical University, Wenhua Road 103, Shenyang, Liaoning 110016, China. Electronic address: zhangteng1200@sina.com.
  • Liu J; Mailman Research Center, McLean Hospital, Harvard Medical School, Boston, MA, United States. Electronic address: liujing@mclean.harvard.edu.
  • Dai R; School of Pharmacy, Shenyang Pharmaceutical University, Wenhua Road 103, Shenyang, Liaoning 110016, China. Electronic address: ronghuadai@sina.com.
Phytomedicine ; 93: 153813, 2021 Dec.
Article in En | MEDLINE | ID: mdl-34735909
ABSTRACT

BACKGROUND:

The bioactive alkaloids identified from Cortex Phellodendri (CP) were highly effective in treating rats with benign prostatic hyperplasia (BPH). Specifically, lipoxygenase-5 (LOX-5) and cyclooxygenase-2 (COX-2) were identified as two primary targets for alleviating inflammation in BPH rats. However, it remains unknown whether the alkaloid components in CP can interact with the two target proteins.

PURPOSE:

To further identify bioactive alkaloids targeting LOX/COX pathways.

METHODS:

An affinity-ultrafiltration mass spectrometry approach was employed to screen dual-target LOX-5/COX-2 ligands from alkaloid extract. The structures of bioactive alkaloids were characterized by high-resolution Fourier transform ion cyclotron resonance mass spectrometry. To understand the molecular mechanisms underlying the effects of bioactive alkaloids, the expression levels of LOX-5 and COX-2 in BPH model rats were investigated at both protein and mRNA levels. The LOX-5/COX-2 enzymes activity experiments and molecular docking analysis were performed to fully evaluate the interactions between bioactive alkaloids and LOX-5/COX-2.

RESULTS:

After comprehensive analysis, the results showed that bioactive alkaloids could suppress the expression of LOX-5 and COX-2 simultaneously to exert an anti-inflammatory effect on the progression of BPH. In addition, the screened protoberberine, demethyleneberberine was found to exhibit prominent inhibitory activities against both LOX-5 and COX-2 enzymes, palmatine and berberine with moderate inhibitory activities. Molecular docking analysis confirmed that demethyleneberberine could interact well with LOX-5/COX-2.

CONCLUSION:

This study is the first to explore the inhibitory effects of bioactive alkaloids from CP on LOX-5 and COX-2 activities in BPH rats. Our findings demonstrate that the bioactive alkaloids from CP can ameliorate BPH via dual LOX-5/COX-2 pathways, which serves as an efficient approach for the discovery of novel drug leads from natural products with reduced side effects.
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Full text: 1 Database: MEDLINE Main subject: Prostatic Hyperplasia / Alkaloids Type of study: Prognostic_studies Language: En Journal: Phytomedicine Year: 2021 Type: Article Affiliation country: China

Full text: 1 Database: MEDLINE Main subject: Prostatic Hyperplasia / Alkaloids Type of study: Prognostic_studies Language: En Journal: Phytomedicine Year: 2021 Type: Article Affiliation country: China