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. 2022 Jan 29;388(1):181–194. doi: 10.1007/s00441-022-03587-z

Fig. 8.

Fig. 8

Esomeprazole-suppressed autophagy induced by L-NAME via AMPKα-mTOR in PE mice. (a) LC3B proteins levels in placentas of control, L-NAME-treated, or L-NAME + esomeprazole-treated mice were detected by Western blot. (a′) Plot depicting the quantification of LC3B protein levels. (bd″) LC3B in placentas of control, L-NAME-treated, or L-NAME + esomeprazole-treated mice were evaluated by immunofluorescence staining. (e) The protein levels of phospho-AMPKα, AMPKα, PPARγ, SirT1, mTOR, and phospho-mTOR in placentas of control, L-NAME-treated, or L-NAME + esomeprazole-treated mice were detected by Western blot. (ff⁗) Quantification of the LC3B, HIF1α, pAMPKα/AMPKα, PPARγ, and phospho-mTOR/mTOR in placentas of control, L-NAME-treated, or L-NAME + esomeprazole-treated mice, N = 3 mice per group, *P < 0.05, **P < 0.01