Related Experiment Video
Updated: Nov 7, 2025

Live Imaging and Quantification of Viral Infection in K18 hACE2 Transgenic Mice Using Reporter-Expressing Recombinant SARS-CoV-2
Published on: November 5, 2021
L-Carnitine Tartrate Downregulates the ACE2 Receptor and Limits SARS-CoV-2 Infection
Aouatef Bellamine1, Tram N Q Pham2, Jaspreet Jain2
1Lonza Consumer Health, Morristown, NJ 07960, USA.
Abstract:
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has been responsible for one of the worst pandemics in modern history. Several prevention and treatment strategies have been designed and evaluated in recent months either through the repurposing of existing treatments or the development of new drugs and vaccines. In this study, we show that L-carnitine tartrate supplementation in humans and rodents led to significant decreases of key host dependency factors, notably angiotensin-converting enzyme 2 (ACE2), transmembrane protease serine 2 (TMPRSS2), and Furin, which are responsible for viral attachment, viral spike S-protein cleavage, and priming for viral fusion and entry. Interestingly, pre-treatment of Calu-3, human lung epithelial cells, with L-carnitine tartrate led to a significant and dose-dependent inhibition of the infection by SARS-CoV-2. Infection inhibition coincided with a significant decrease in ACE2 mRNA expression levels. These data suggest that L-carnitine tartrate should be tested with appropriate trials in humans for the possibility to limit SARS-CoV-2 infection.
Insights
L-carnitine tartrate supplementation reduced key SARS-CoV-2 host factors like ACE2 and TMPRSS2 in humans and rodents. This suggests L-carnitine tartrate may be a potential therapeutic to limit SARS-CoV-2 infection.
Area of Science:
- Virology
- Molecular Biology
- Pharmacology
Background:
- Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) caused a global pandemic, necessitating novel treatment strategies.
- Existing treatments and vaccines are being explored, alongside new drug development.
- Host dependency factors are critical for viral entry and replication.
Purpose of the Study:
- To investigate the effect of L-carnitine tartrate on SARS-CoV-2 host dependency factors.
- To evaluate L-carnitine tartrate's potential to inhibit SARS-CoV-2 infection in vitro.
- To explore L-carnitine tartrate as a potential therapeutic intervention for SARS-CoV-2.
Main Methods:
- Supplementation with L-carnitine tartrate in humans and rodents.
- Measurement of key host dependency factors: angiotensin-converting enzyme 2 (ACE2), transmembrane protease serine 2 (TMPRSS2), and Furin.
- In vitro infection assays using Calu-3 human lung epithelial cells pre-treated with L-carnitine tartrate.
- Analysis of ACE2 mRNA expression levels.
Main Results:
- L-carnitine tartrate supplementation significantly decreased ACE2, TMPRSS2, and Furin levels.
- Pre-treatment with L-carnitine tartrate dose-dependently inhibited SARS-CoV-2 infection in Calu-3 cells.
- Inhibition of infection correlated with reduced ACE2 mRNA expression.
Conclusions:
- L-carnitine tartrate demonstrates potential in reducing key factors essential for SARS-CoV-2 entry.
- L-carnitine tartrate exhibits in vitro efficacy in inhibiting SARS-CoV-2 infection.
- Further clinical trials are warranted to assess L-carnitine tartrate's therapeutic value against SARS-CoV-2.
Related Concept Videos
Antihypertensive Drugs: Angiotensin-Converting Enzyme Inhibitors
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System
GPCRs Regulate Adenylyl Cylase Activity

