A study of lovastatin and l-arginine co-loaded PLGA nanomedicine for enhancing nitric oxide production and eNOS expression. Issue 4 (7th January 2022)
- Record Type:
- Journal Article
- Title:
- A study of lovastatin and l-arginine co-loaded PLGA nanomedicine for enhancing nitric oxide production and eNOS expression. Issue 4 (7th January 2022)
- Main Title:
- A study of lovastatin and l-arginine co-loaded PLGA nanomedicine for enhancing nitric oxide production and eNOS expression
- Authors:
- Wijaya, Andy
Wang, Yi
Tang, Dan
Zhong, Yuan
Liu, Boyan
Yan, Meng
Jiu, Quhui
Wu, Wei
Wang, Guixue - Abstract:
- Abstract : LA and LV were co-loaded in PLGA NPs. PLGA-LA/LV NPs can suppress the proliferation of VSMCs, enhance eNOS mRNA and protein expression in HUVECs, promote SR-B1 mRNA expression, and lower the total cholesterol of blood plasma in C57BL/6 mice. Abstract : Nitric oxide (NO) is an exceptional endogenous biological gas that mediates and regulates physiological and pathological processes in the human body. However, its synthesis process is impaired during athero-progression and formation. Hence, a strategy to boost NO production and target endothelial nitric oxide synthase (eNOS) is crucial and intriguing in atherosclerosis (AS) management. Herein, we prepare l -arginine (LA) and lovastatin (LV) co-loaded PLGA nanomedicine to achieve sustainable release for enhancing NO production. The utilization of LA reveals that LA has dual contributions, acting as a NO donor and enhancing the solubility of LV by stabilizing PLGA NPs. PLGA-LA/LV demonstrated its potential to boost NO in vitro and in vivo confirmed using DAF-FM DA, augment eNOS and p-eNOS mRNA and protein levels, and suppress the ki67 proliferation marker in VSMCs; in addition, it lowers the total cholesterol level of blood plasma in C57BL/6 mice. Moreover, PLGA can protect the compound delivered and enhance the bioavailability to reach and get released in the blood circulation after oral administration. Collectively, our results endow a safe and efficient nanomedicine outcome, specifically with potential for ASAbstract : LA and LV were co-loaded in PLGA NPs. PLGA-LA/LV NPs can suppress the proliferation of VSMCs, enhance eNOS mRNA and protein expression in HUVECs, promote SR-B1 mRNA expression, and lower the total cholesterol of blood plasma in C57BL/6 mice. Abstract : Nitric oxide (NO) is an exceptional endogenous biological gas that mediates and regulates physiological and pathological processes in the human body. However, its synthesis process is impaired during athero-progression and formation. Hence, a strategy to boost NO production and target endothelial nitric oxide synthase (eNOS) is crucial and intriguing in atherosclerosis (AS) management. Herein, we prepare l -arginine (LA) and lovastatin (LV) co-loaded PLGA nanomedicine to achieve sustainable release for enhancing NO production. The utilization of LA reveals that LA has dual contributions, acting as a NO donor and enhancing the solubility of LV by stabilizing PLGA NPs. PLGA-LA/LV demonstrated its potential to boost NO in vitro and in vivo confirmed using DAF-FM DA, augment eNOS and p-eNOS mRNA and protein levels, and suppress the ki67 proliferation marker in VSMCs; in addition, it lowers the total cholesterol level of blood plasma in C57BL/6 mice. Moreover, PLGA can protect the compound delivered and enhance the bioavailability to reach and get released in the blood circulation after oral administration. Collectively, our results endow a safe and efficient nanomedicine outcome, specifically with potential for AS management. … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 10:Issue 4(2021)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 10:Issue 4(2021)
- Issue Display:
- Volume 10, Issue 4 (2021)
- Year:
- 2021
- Volume:
- 10
- Issue:
- 4
- Issue Sort Value:
- 2021-0010-0004-0000
- Page Start:
- 607
- Page End:
- 624
- Publication Date:
- 2022-01-07
- Subjects:
- Materials -- Periodicals
Chemistry, Analytic -- Periodicals
Biomedical materials -- Research -- Periodicals
543.0284 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/tb# ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d1tb01455b ↗
- Languages:
- English
- ISSNs:
- 2050-750X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5012.205200
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 21102.xml