Circulating and vein wall P-selectin promote venous thrombogenesis during aging in a rodent model

The objective of this study was to identify the direct relationship between aging and selectin activation during acute venous thrombosis in mice of varying ages. We hypothesized that older animals would have increased venous thrombus formation as a result of age associated-increases of pro-inflammatory molecules within the vein wall when compared to younger animals.

Deep venous thrombosis (DVT) was induced in 4 and 18month old C57BL/6 mice using the electrolytic inferior vena cava model (EIM) of DVT. Blood and tissue samples were collected at baseline (TC), 6hours, and 2days post-thrombosis induction.

Older mice had significantly larger thrombi versus younger mice at 6H (18.4±6.21 vs. 13.0±4.29×10(-3) grams, p=0.0033) and 2D (18.4±4.27 vs. 13.0±5.01×10(-3) grams, p=0.0005), higher soluble P-selectin levels at 6H (13±2.5 vs. 8.4±2.7ng/mg p=0.0010) and 2D (12.7±5.0 vs. 5.9±1.3ng/mg p=0.0020), and higher vein wall P-selectin levels at 6H (1.94×10(5)±3.56×10(4) vs. 4.81±2.29×10(4) pg/mg p=0.0001) and 2D (1.38×10(5)±5.65×10(4) vs. 3.73±1.66×10(4) pg/mg p=0.0177). Older animals also had significantly higher platelet numbers at 6H (841±203.8 vs. 564±164.8K/μL p=0.0001), and 2D (1002±342.9 vs. 690±186.1K/μL p=0.0003), with corresponding increases in mean platelet volume versus younger mice post thrombosis (p≤0.01).

Older animals had significantly larger venous thrombi versus younger animals post-thombosis, as a result of high levels of P-selectin both in the circulation and locally at the level of the vein wall. Expression of local and soluble P-selectin increased with age, resulting in a pro-thrombotic environment not represented in younger mice.