Intraperitoneal delivery of cannabidiol (CBD) and Δ9-tetrahydocannabinol (THC) promotes papillomavirus infections in athymic nude mice

IF 8.1 Q1 VIROLOGY Tumour Virus Research Pub Date : 2025-06-01 Epub Date: 2024-12-16 DOI:10.1016/j.tvr.2024.200307
Sarah A. Brendle , Jingwei Li , Dongxiao Sun , Junjia Zhu , Angela N. Henderson-Redmond , Daniel J. Morgan , Karla K. Balogh , Danielle Covington , Debra A. Shearer , Jiafen Hu
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Abstract

We used our mouse papillomavirus (MmuPV1) model to test the hypothesis that two primary psychoactive ingredients of marijuana, Δ9-tetrahydrocannabinol (THC) and cannabidiol (CBD), promote papillomavirus persistence in the oral mucosa of infected mice. We conducted intraperitoneal (ip) injections of a moderate dose (3 mg/kg) of either CBD and/or THC in both male and female athymic nude mice and followed the mice up to 20 weeks post-infection. These doses are comparable to what is estimated for human conventional cannabis consumption. All mice were infected with MmuPV1 in the oral cavity at week 4 post-ip delivery of CBD, THC, or a combination of THC and CBD (T + C). THC and CBD were detected in the blood of treated mice for up to 72 h after ip injection. Significantly higher levels of viral DNA were detected in males from both CBD and T + C-treated groups compared to those in the control group at 9- 10-and 12-weeks post infection. A marginally increased viral RNA was also detected in the infected tongues of males in all tested groups compared to that in males in the vehicle control group; the opposite was observed in females. We detected significantly higher levels of dermal dendritic cells (CD205+CD11c+), granulocytes (Ly6G+), but macrophages (F4-80+) recruited to the infected tongues of CBD-treated females. Our findings suggest that CBD may play a role in promoting MmuPV1 persistence in the oral cavity.
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腹腔注射大麻二酚(CBD)和Δ9-tetrahydocannabinol (THC)促进乳突裸鼠乳头瘤病毒感染。
我们使用小鼠乳头瘤病毒(MmuPV1)模型来验证大麻的两种主要精神活性成分Δ9-tetrahydrocannabinol (THC)和大麻二酚(CBD)促进乳头瘤病毒在感染小鼠口腔黏膜中的持续存在的假设。我们对雄性和雌性胸腺裸小鼠进行了中等剂量(3mg /kg)的CBD和/或THC腹腔注射,并随访小鼠至感染后20周。这些剂量与估计的人类传统大麻消费量相当。所有小鼠在注射CBD、四氢大麻酚或四氢大麻酚和CBD联合(T+C)后第4周在口腔感染MmuPV1。注射ip后72小时,在治疗小鼠血液中检测到THC和CBD。在感染后9- 10周和12周,与对照组相比,在CBD和T+ c治疗组的男性中检测到的病毒DNA水平明显更高。与载体对照组相比,在所有测试组的男性感染舌头中检测到的病毒RNA也略有增加;在女性身上观察到的情况正好相反。我们检测到真皮树突状细胞(CD205+CD11c+)、粒细胞(Ly6G+)水平明显升高,但巨噬细胞(F4-80+)被招募到经cbd治疗的雌性感染舌头上。我们的研究结果表明,CBD可能在促进mupv1在口腔中的持久性中发挥作用。
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来源期刊
Tumour Virus Research
Tumour Virus Research Medicine-Infectious Diseases
CiteScore
6.50
自引率
2.30%
发文量
16
审稿时长
56 days
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