I definitely agree that a Coronary Calcium Scan score of 880 is a huge concern.
Let me clarify what I meant by opening my veins… and reduction in varicose veins.
Prior to Rapamycin my veins were not as prominent. And, there were obvious little kinks in the veins every inch to two inches. I am sure there is a medical name… after being on rapamycin 6 months… my veins started to pop… a sign of low body fat and good health not only my veins but the subcutaneous structures are visible. And, all the kinks straightened and were gone. That is how they opened.
My veins are always pumped 24/7.
Varicose veins just after rapamycin… improved… but not great.
Me 7 years ago… no pumped veins to be seen… lol. My question is how can I in this obese state have a calcium score of zero? Heart under 35 years old. Did rapamycin the previous 2 years help repair… when it was straightening my kinked veins? I don’t know.
Rapamycin can stop the advance of arthrocleurosis… but can it reduce arthrocleurosis? Somewhere it said possibly. Need to hunt that up.
Rapamycin-Loaded Biomimetic Nanoparticles Reverse Vascular Inflammation
Abstract

Rationale:
Through localized delivery of rapamycin via a biomimetic drug delivery system, it is possible to reduce vascular inflammation and thus the progression of vascular disease.
Objective:
Use biomimetic nanoparticles to deliver rapamycin to the vessel wall to reduce inflammation in an in vivo model of atherosclerosis after a short dosing schedule.
Methods and Results:
Biomimetic nanoparticles (leukosomes) were synthesized using membrane proteins purified from activated J774 macrophages. Rapamycin-loaded nanoparticles were characterized using dynamic light scattering and were found to have a diameter of 108±2.3 nm, a surface charge of −15.4±14.4 mV, and a polydispersity index of 0.11 +/ 0.2. For in vivo studies, ApoE−/− mice were fed a high-fat diet for 12 weeks. Mice were injected with either PBS, free rapamycin (5 mg/kg), or rapamycin-loaded leukosomes (Leuko-Rapa; 5 mg/kg) once daily for 7 days. In mice treated with Leuko-Rapa, flow cytometry of disaggregated aortic tissue revealed fewer proliferating macrophages in the aorta (15.6±9.79 %) compared with untreated mice (30.2±13.34 %) and rapamycin alone (26.8±9.87 %). Decreased macrophage proliferation correlated with decreased levels of MCP (monocyte chemoattractant protein)-1 and IL (interleukin)-b1 in mice treated with Leuko-Rapa. Furthermore, Leuko-Rapa–treated mice also displayed significantly decreased MMP (matrix metalloproteinases) activity in the aorta (mean difference 2554±363.9, P=9.95122×10−6). No significant changes in metabolic or inflammation markers observed in liver metabolic assays. Histological analysis showed improvements in lung morphology, with no alterations in heart, spleen, lung, or liver in Leuko-Rapa–treated mice.
Conclusions:
We showed that our biomimetic nanoparticles showed a decrease in proliferating macrophage population that was accompanied by the reduction of key proinflammatory cytokines and changes in plaque morphology. This proof-of-concept showed that our platform was capable of suppressing macrophage proliferation within the aorta after a short dosing schedule (7 days) and with a favorable toxicity profile. This treatment could be a promising intervention for the acute stabilization of late-stage plaques.