“…Directly or indirectly, these xenobiotics can impair glucose metabolism by affecting β islet cell homeostasis [ 85 , 86 , 90 ] and mitochondrial function in an ROS-dependent manner, culminating in insulin resistance and Diabetes Mellitus type II onset [ 95 , 100 , 135 ]. Finally, the kidneys are affected by the systemic inflammatory response, increased blood pressure, and higher levels of ROS, which increase mesangial cell proliferation, activate programmed cell death pathways on tubular cells, and impair mitochondrial function [ 109 , 110 , 111 , 112 , 113 , 114 , 115 , 135 , 136 , 137 ]. Once the kidneys are responsible for filtration, these xenobiotics accumulate on renal structures and cause inflammation and oxidative stress.…”