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. 2020 Apr 23;15(4):e0231495. doi: 10.1371/journal.pone.0231495

Table 2. Summary of histopathological findings in Gd-treated and control mice (N = 9 and 8, respectively).

ID age [w] Brain heart lung liver spleen kidney GIT
control 360 94,3 - - - vvv - - -
361 94,3 - - - Vvv - ii -
362 94,3 - - - Vv c i -
363 94,3 - - - Vv c vascular pathology ii -
364 94,3 - hemorrhage in 4th ventricle - i Vvv c ii -
366 94,3 - - - Vvv - ii -
367 94,3 - - - Vvv - - -
368 94,3 - - - Vvv - - -
476 94,9 - mild gliosis (GFAP) - ii Vv cc iii -
Gd-exposure 389 93,7 autolytic
393 94,3 - - - hemorrhage Vvv c i -
394 90,0 autolytic
395 94,3 - - - Vv c i -
396 94,3 - - - Vvv c - -
490 94,9 - - ii Vv ccc i -
491 94,9 - - ii tumor vv cellular inflitrates cc i -
493 94,9 - mild gliosis (GFAP) - ii Vv - - -

In general, mice did not show pathological alterations in heart or gastrointestinal tract (GIT). No gross cellular alterations could be found in the CNS, despite two mice (N = 1 within each group) showing mild gliosis in the hippocampus (g). Cellular infiltrates could be found in the lung and kidneys (i). The liver showed hepatocellular vacuolization due to fatty change (v). A loss of nucleated cells could be found in the red pulp of the spleen (c). All pathological alterations could be found to a mild, moderate, or severe extent, respectively (x, xx, xxx). Two mice died before the planned end point and could not be examined because of necrotic changes in nearly all organs due to autolysis.