In mice, beta-caryophyllene reduced CKD-related lung inflammation

Beta-caryophyllene reduces lung inflammation secondary to chronic kidney disease.

Biochemical and biophysical research communications • • Highly Relevant
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AI Summary

This abstract-based summary describes an animal study asking whether β-caryophyllene (βC), a CB2 receptor agonist and plant terpene, could reduce lung changes caused by chronic kidney disease (CKD). Male Swiss mice underwent a 5/6 partial nephrectomy to model CKD and were assigned to sham surgery, CKD with vehicle, or CKD treated with 10 mg/kg/day of βC from days 7 to 14 after surgery. Lung, blood, and other samples were collected on day 15; the abstract does not report the number of animals or quantitative effect sizes.

Compared with sham-operated mice, CKD-model mice showed greater inflammatory-cell accumulation in the lungs, increased myeloperoxidase activity and protein leakage, tissue injury, excess superoxide production, and higher ICAM-1 expression. βC attenuated inflammatory-cell infiltration, protein extravasation, and ICAM-1 expression, while also improving reported measures of kidney function. However, CB2 receptor expression itself did not differ between groups. Because this was a short-term mouse study, it cannot establish that β-caryophyllene would treat CKD-related lung injury in people; the abstract also says the renal improvement may have contributed to the lung effects. This is an abstract-based summary, not a review of the full text.

💡 Key Findings

1
In a mouse model of CKD created by 5/6 partial nephrectomy, β-caryophyllene was tested at 10 mg/kg/day against vehicle and sham controls.
High
90%
2
CKD increased lung inflammation and injury markers, including leukocyte infiltration, myeloperoxidase activity, protein leakage, excess superoxide, and ICAM-1 expression.
High
85%
3
β-caryophyllene attenuated inflammatory-cell infiltration, protein extravasation, and ICAM-1 expression in the lungs of CKD-model mice.
Good
70%
4
β-caryophyllene improved reported kidney-function parameters, which the authors suggest may have contributed partly to the reduction in lung inflammation; CB2 receptor expression did not differ between groups.
Good
65%

📄 Original Abstract

BACKGROUND: Chronic kidney disease (CKD) causes millions of deaths and is a known risk factor for the development of other diseases. CKD has been associated with lung injury characterized by neutrophil infiltration and edema. Despite evidence that the lungs are distant organs affected in CKD, there is no treatment to impair lung injury. Cannabinoid receptors type 2 (CB2) activation has been shown to reduce renal dysfunction and organ damage in sepsis. OBJECTIVE: Therefore, this study aimed to evaluate the effects of β-caryophyllene (βC), a CB2 agonist, on CKD-induced pulmonary alterations. METHODS: Male Swiss mice were subjected to 5/6th partial nephrectomy (PNx) model and randomly assigned to three experimental groups: sham, PNx + vehicle and PNx+βC (10 mg/kg/day). Treatment was administered from days 7 to 14 post-surgery. On day 15, bronchoalveolar lavage, blood, and organs were obtained. RESULTS: PNx animals exhibited increased pulmonary leukocyte infiltration, MPO activity, and protein content. Histological analysis of lung tissue showed signs of injury and excessive superoxide production. Increased expression of ICAM-1 was also detected by Western blotting in the lungs of PNx animals. βC treatment attenuated inflammatory cell infiltration and protein extravasation, and reduced ICAM-1 expression in lungs of CKD mice. βC improved renal function parameters, which may have contributed, at least in part, to the reduction in lung inflammation. CB2 receptors expression did not differ among the groups. CONCLUSION: In conclusion, βC attenuated PNx-induced pulmonary changes, supporting its potential as an adjuvant therapy for lung injury in CKD.

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