Exploring the Antibacterial Potential of Semisynthetic Phytocannabinoid: Tetrahydrocannabidiol (THCBD) as a Potential Antibacterial Agent against Sensitive and Resistant Strains of Staphylococcus aureus

被引:7
|
作者
Cham, Pankaj Singh [1 ,5 ]
Deepika [2 ,3 ,5 ]
Bhat, Rahul [2 ,3 ,5 ]
Raina, Diksha [2 ,3 ,5 ]
Manhas, Diksha [4 ,5 ]
Kotwal, Pankul [4 ,5 ]
Mindala, Durga Prasad [1 ,5 ]
Pandey, Noopur [6 ]
Ghosh, Animesh [6 ]
Saran, Saurabh [2 ,3 ,5 ]
Nandi, Utpal [4 ,5 ]
Khan, Inshad Ali [2 ,7 ]
Singh, Parvinder Pal [1 ,5 ]
机构
[1] CSIR Indian Inst Integrat Med CSIR IIIM, Nat Prod & Med Chem Div, Jammu 180001, India
[2] CSIR Indian Inst Integrat Med CSIR IIIM, Clin Microbiol Div, Jammu 180001, India
[3] CSIR Indian Inst Integrat Med CSIR IIIM, Fermentat & Microbial Biotechnol Div, Jammu 180001, India
[4] CSIR Indian Inst Integrat Med CSIR IIIM, Pharmacol Div, Canc Pharmacol Div, Jammu 180001, India
[5] Acad Sci & Innovat Res AcSIR, Ghaziabad 201002, India
[6] Birla Inst Technol Mesra, Dept Pharmaceut Sci & Technol, Solid State Pharmaceut Res Lab, Ranchi 835215, Jharkhand, India
[7] Cent Univ Rajasthan, Sch Life Sci, Dept Microbiol, Ajmer 305817, Rajasthan, India
来源
ACS INFECTIOUS DISEASES | 2023年 / 10卷 / 01期
关键词
phytocannabinoid; tetrahydrocannabidiol; reduction; antibacteriallead; resistant; Staphylococcusaureus; ANTIBIOTIC-RESISTANCE; CANNABINOID RECEPTOR; BIOLOGICAL-ACTIVITY; CANNABIDIOL; EFFICACY; CANNABICHROMENE; TOXICITY; EFFLUX;
D O I
10.1021/acsinfecdis.3c00154
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Antimicrobial resistance (AMR) is one of the most challenging problems and is responsible for millions of deaths every year. We therefore urgently require new chemical entities with novel mechanisms of action. Phytocannabinoids have been adequately reported for the antimicrobial effect but not seriously pursued because of either stringent regulatory issues or poor drug-like properties. In this regard, the current work demonstrated the antibacterial potential of tetrahydrocannabidiol (THCBD, 4), a semisynthetic phytocannabinoid, against Staphylococcus aureus, the second-most widespread bug recognized by the WHO. THCBD (4) was generated from cannabidiol and subjected to extensive antibacterial screening. In in vitro studies, THCBD (4) demonstrated a potent MIC of 0.25 mu g/mL against Gram-positive bacteria, S. aureus ATCC-29213. It is interesting to note that THCBD (4) has demonstrated strong effectiveness against efflux pump-overexpressing (SA-1199B, SA-K2191, SA-K2192, and Mup (R)-1) and multidrug-resistant (MRSA-15187) S. aureus strains. THCBD (4) has also shown a good effect in kill kinetic assays against ATCC-29213 and MRSA-15187. In the checkerboard assay, THCBD (4) has shown additive/indifference effects with several well-known clinically used antibiotics, tetracycline, mupirocin, penicillin G, and ciprofloxacin. THCBD (4) also exhibited good permeability in the artificial skin model. Most importantly, THCBD (4) has significantly reduced CFU in mice's in vivo skin infection models and also demonstrated decent plasma exposure with 16-17% oral bioavailability. Acute dermal toxicity of THCBD (4) suggests no marked treatment-related impact on gross pathophysiology. This attractive in vitro and in vivo profile of plant-based compounds opens a new direction for new-generation antibiotics and warrants further detailed investigation.
引用
收藏
页码:64 / 78
页数:15
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