4.6 Article

Pro-Inflammatory Interactions of Dolutegravir with Human Neutrophils in an In Vitro Study

期刊

MOLECULES
卷 27, 期 24, 页码 -

出版社

MDPI
DOI: 10.3390/molecules27249057

关键词

cytosolic calcium; elastase; HIV; ionophore; pro-inflammatory activity

资金

  1. National Health Laboratory Research Trust of South Africa
  2. National Research Foundation of South Africa
  3. [004 94713]

向作者/读者索取更多资源

A study suggests that the HIV integrase inhibitor, dolutegravir, may be associated with weight gain and the development of metabolic syndrome. This could be due to the pro-inflammatory effects of dolutegravir leading to systemic inflammation. The study found that dolutegravir can stimulate neutrophils to produce reactive oxygen species and increase the release of elastase, which may contribute to insulin resistance and weight gain.
There is increasing awareness of an association between the uptake of the HIV integrase inhibitor, dolutegravir, in first-line antiretroviral regimens with unusual weight gain and development of the metabolic syndrome, particularly in African women. Although seemingly unexplored, the development of systemic inflammation linked to the putative pro-inflammatory activity of dolutegravir represents a plausible pathophysiological mechanism of this unusual weight gain. This possibility was explored in the current study undertaken to investigate the effects of dolutegravir (2.5-20 mu g/mL) on several pro-inflammatory activities of neutrophils isolated from the blood of healthy, adult humans. These activities included the generation of reactive oxygen species (ROS), degranulation (elastase release) and alterations in the concentrations of cytosolic Ca2+ using chemiluminescence, spectrophotometric and fluorimetric procedures, respectively. Exposure of neutrophils to dolutegravir alone resulted in the abrupt, dose-related, and significant (p < 0.0039-p < 0.0022) generation of ROS that was attenuated by the inclusion of the Ca2+-chelating agent, EGTA, or inhibitors of NADPH oxidase (diphenyleneiodonium chloride, DPI), phospholipase C (U733122), myeloperoxidase (sodium azide) and phosphoinositol-3-kinase (wortmannin). In addition, exposure to dolutegravir augmented the release of elastase by stimulus-activated neutrophils. These pro-inflammatory effects of dolutegravir on neutrophils were associated with significant, rapid, and sustained increases in the concentrations of cytosolic Ca2+ that appeared to originate from the extracellular compartment, seemingly consistent with an ionophore-like property of dolutegravir. These findings are preliminary and necessitate verification in the clinical setting of HIV infection. Nevertheless, given the complex link between inflammation and obesity, these pro-inflammatory interactions of dolutegravir with neutrophils may contribute to unexplained weight gain, possibly via the development of insulin resistance.

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