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临床试验/NCT06355167
NCT06355167已完成不适用

Interventional, Open-label Study of the Effect of an Aquaporin-1 Inhibitor, the Bacopaside II Contained in Bacopa-400® , on Oxidative Stress in Healthy Volunteers: BacOxy_I Study

Cliniques universitaires Saint-Luc- Université Catholique de Louvain2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2022年3月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
20
试验地点
2
主要终点
Plasma lipid peroxydes

研究概览

简要总结

Bacoxy_I study aims to evaluate the efficacy of a standardized Bacopa monnieri extract, Bacopa-400®, on vascular oxidative stress.

详细描述

The Bacopa-400® is a standardized extract of a plant called Bacopa Monnieri, which mainly grows in India and neighboring countries. The virtues of this plant, also called Brahmi, have been used in Ayurvedic medicine for millennia in the treatment of chronic neurological diseases accompanied by cognitive impairment and memory disorders, as well as for stress management. Several companies have subsequently improved the preparation of standardized extracts of Bacopa Monnieri. Bacopa-400® from the Belgian firm Deba Pharma™ was selected because it adheres to good manufacturing practices (GMP). Currently, there are over 289 studies listed regarding the positive role of Bacopa monnieri in cognitive functions in both young and elderly subjects. Furthermore, no major side effects have been reported following the use of this plant extract in acute or chronic administration in hundreds of people of all ages.

Bacopa monnieri plant contains several bacosides, including the Bacopaside II a specific inhibitor of the water channel Aquaporin 1 (AQP1). AQP1 is part of the aquaporin family responsible for bidirectional transmembrane water transport. It is the most abundant aquaporin in mammalian cardiovascular tissue, present in myocardial cells, endothelial cells, and red blood cells. AQP1, more than a water channel, is also a peroxiporin able to facilitate the passage of hydrogen peroxide (H2O2), involved in oxidative stress.

In previous work, the Pharmacology and Therapeutics (FATH) department from UCLouvain (Brussels) discovered the protective effect of Bacopaside II on cardiovascular oxidative stress. Through a series of experiments, it was demonstrated that Bacopaside II dose dependently attenuates the passage of H2O2 into cardiac myocytes, thus preventing hypertrophy induced by neurohormones. Additionally, in murine models, oral administration of Bacopa monnieri extract attenuated cardiac hypertrophy triggered by hypertrophic stimuli. This cardiac protection occurs through inhibition of AQP1.

Based on this premises, a clinical investigation was undertaken to explore the potential of Bacopa-400® in attenuating vascular oxidative stress among healthy volunteers. This interventional, open-label and monocentric comprised two groups. Group A received a daily dose of 400 mg and Group B a daily dose of 800 mg over a 6-week period, followed by a 4-week observation period after the cessation of treatment.

The primary objective of this study was to assess the impact of Bacopa-400® on oxidative stress in healthy individuals and determine the optimal dosage for maximal efficacy. Furthermore, the study analyzed the incidence, severity, and frequency of adverse events, including suspected unexpected serious adverse events (SUSAR).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Healthy volunteers
  • Effective contraception

排除标准

  • Any chronic disease
  • Any chronic use of drug
  • Pregnancy and breast feeding
  • Gastro-intestinal diseases (e.g. ulcer, gastro-oesophageal reflux, lactose intolerance)

结局指标

主要结局

Plasma lipid peroxydes

时间窗: Baseline (V0), 2 weeks (V2), 6 weeks (V4), 10 weeks (V6)

Lipid peroxidation (µM) is a form of oxidative damage that impacts cellular membranes, lipoproteins, and other lipid-containing molecules under conditions of oxidative stress. Assessing changes in lipid peroxide levels during the study served as a reflection of oxidative status. Plasma lipid peroxides were quantified using a colorimetric test using the 3,3',5,5'-tetramethylbenzidine (TMB).

Nitrosylated hemoglobin (HbNO) in red blood cells

时间窗: Baseline (V0), 6 weeks (V4), 10 weeks (V6)

Vascular oxidative stress is involved in the decreased of nitric oxide (NO) bioavailability. Erythrocyte 5-α-coordinate nitrosyl-hemoglobin or nitrosylated hemoglobin (HbNO) is a complexe between NO and deoxyhemoglobin serving as a marker for NO bioavailability. HbNO levels (nM) were quantified using electron paramagnetic resonance spectroscopy

Ex vivo DCFDA test on red blood cells (RBCs)

时间窗: Baseline (V0), 2 weeks (V2), 6 weeks (V4), 10 weeks (V6)

DCFA (dichlorofluorescein diacetate) is a probe used to assess the presence of intracellular reactive oxygen species (ROS). Red blood cells are incubated with DCFA and extracellular hydrogen peroxide (H2O2). After passive diffusion into the cells and upon encountering ROS, DCFDA undergoes conversion to produce a highly fluorescent compound, the DCF (2',7'-Dichlorofluorescein). This resulting fluorescence intensity (arbitrary unit) was quantified using FACS. This technique allowed us to measure kinetically the entry of ROS as H2O2 in RBCs.

Methemoglobin in red blood cells

时间窗: Baseline (V0), 6 weeks (V4), 10 weeks (V6)

Methemoglobin is the oxidized form of hemoglobin, where the iron atom in the heme group is oxidized from the ferrous to the ferric state. Exposure to oxidative stress can lead to the formation of methemoglobin making the latter a biomarker of vascular oxidative stress. Methemoglobin levels (arbitrary unit) were measured by electron paramagnetic resonance spectroscopy.

次要结局

  • Red blood cells count(Baseline (V0), 2 weeks (V2), 6 weeks (V4), 10 weeks (V6))
  • haemoglobin(Baseline (V0), 2 weeks (V2), 6 weeks (V4), 10 weeks (V6))
  • haematocrit(Baseline (V0), 2 weeks (V2), 6 weeks (V4), 10 weeks (V6))
  • Sodium(Baseline (V0), 2 weeks (V2), 6 weeks (V4), 10 weeks (V6))
  • Low-Density Lipoprotein (LDL) cholesterol(Baseline (V0), 2 weeks (V2), 6 weeks (V4), 10 weeks (V6))
  • Creatinine(Baseline (V0), 2 weeks (V2), 6 weeks (V4), 10 weeks (V6))
  • Potassium(Baseline (V0), 2 weeks (V2), 6 weeks (V4), 10 weeks (V6))
  • Bicarbonate(Baseline (V0), 2 weeks (V2), 6 weeks (V4), 10 weeks (V6))
  • Total cholesterol(Baseline (V0), 2 weeks (V2), 6 weeks (V4), 10 weeks (V6))
  • High-Density Lipoprotein (HDL) cholesterol(Baseline (V0), 2 weeks (V2), 6 weeks (V4), 10 weeks (V6))
  • Triglycerides(Baseline (V0), 2 weeks (V2), 6 weeks (V4), 10 weeks (V6))
  • aspartate aminotransferase (ASAT), (U/L)(Baseline (V0), 2 weeks (V2), 6 weeks (V4), 10 weeks (V6))
  • alanine aminotransferase (ALAT) (U/L)(Baseline (V0), 2 weeks (V2), 6 weeks (V4), 10 weeks (V6))
  • gamma-glutamyl-transferase (GGT) level(Baseline (V0), 2 weeks (V2), 6 weeks (V4), 10 weeks (V6))
  • Glomerular filtration rate(Baseline (V0), 2 weeks (V2), 6 weeks (V4), 10 weeks (V6))

研究者

发起方
Cliniques universitaires Saint-Luc- Université Catholique de Louvain
申办方类型
Other
责任方
Principal Investigator
主要研究者

Montiel Virginie

Head of the intensive care unit

Cliniques universitaires Saint-Luc- Université Catholique de Louvain

研究点 (2)

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