Table 1 of Hill, Mol Vis 2018; 24:712-726.


Table 1. Experimental design.

Number of rats Treatment group (n=number of eyes/group) Measured endpoints
12 rats IV Vehicle (n=4)
5 ul IV siEGFP (20ng; n=4)
5 ul IV siRhoA (10ng; n=4)
5 ul IV siEGFP (15ng; n=4)
5 ul IV siRhoA (20ng; n=4)
5 ul IV siRhoA (30ng; n=4)
5 ul IV siRhoA (40ng; n=4) RT–PCR (to assess knockdown efficiency and the activation of innate immunity)
3 Rats Intact control eyes (n=3) IHC (contractility & fibrosis)
4 Rats 3.5 ul IC of 5ng/µl TGFβ1 (n=4) 7d IHC (contractility & fibrosis)
3.5 ul IC 3.5ul PBS (n=4) 7d IHC (contractility & fibrosis)
4 Rats 3.5 ul IC 5ng/µl TGFβ1 (n=4) 35d IHC (contractility & fibrosis)
3.5 ul IC PBS (n=4) 35d IOP; IHC (contractility & fibrosis)
6 Rats 3.5 ul IC 5ng/µl TGFβ1+5ng/µl siRhoA (n=6) 7d IOP; IHC (contractility & fibrosis)
IC 5 ng/µl TGFβ1+5ng/µl siEGFP (n=6) 7d IOP; IHC (contractility & fibrosis)
6 Rats IC 5 ng/µl TGFβ1+5ng/µl siRhoA (n=6) 35d IOP; IHC (contractility & fibrosis)
IC 5 ng/µl TGFβ1+5ng/µl siEGFP (n=6) 35d IOP; IHC (contractility & fibrosis)