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Original Article

Herba Cistanche extract enhances mitochondrial glutathione status and respiration in rat hearts, with possible induction of uncoupling proteins

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Pages 512-517 | Received 26 Nov 2008, Accepted 05 Mar 2009, Published online: 28 Apr 2010

Figures & data

Figure 1. A methanol extract of Herba Cistanche affects mitochondrial reduced glutathione levels in rat hearts. Animals were orally treated with a methanol extract of Herba Cistanche at the indicated daily doses for 3 consecutive days. Mitochondrial reduced glutathione (GSH) levels were measured as described in “Materials and methods.” Each bar represents mean ± SEM, with five animals/group. *Significantly different from control group; asignificantly different from group pretreated with 0.5 g/kg extract.

Figure 1.  A methanol extract of Herba Cistanche affects mitochondrial reduced glutathione levels in rat hearts. Animals were orally treated with a methanol extract of Herba Cistanche at the indicated daily doses for 3 consecutive days. Mitochondrial reduced glutathione (GSH) levels were measured as described in “Materials and methods.” Each bar represents mean ± SEM, with five animals/group. *Significantly different from control group; asignificantly different from group pretreated with 0.5 g/kg extract.

Figure 2. A methanol extract of Herba Cistanche affects mitochondrial oxidized glutathione levels in rat hearts. Animals were orally treated with a methanol extract of Herba Cistanche at the indicated daily doses for 3 consecutive days. Mitochondrial oxidized glutathione (GSSG) levels were measured as described in “Materials and methods.” Each bar represents mean ± SEM, with five animals/group. *Significantly different from untreated control group.

Figure 2.  A methanol extract of Herba Cistanche affects mitochondrial oxidized glutathione levels in rat hearts. Animals were orally treated with a methanol extract of Herba Cistanche at the indicated daily doses for 3 consecutive days. Mitochondrial oxidized glutathione (GSSG) levels were measured as described in “Materials and methods.” Each bar represents mean ± SEM, with five animals/group. *Significantly different from untreated control group.

Figure 3. A methanol extract of Herba Cistanche affects mitochondrial Ca2+ content in rat hearts. Rats were fed a methanol extract of Herba Cistanche at 0.5 g/kg and 1.0 g/kg for 3 days. Mitochondrial Ca2+ contents were measured as described in “Materials and methods.” Each bar represents mean ± SEM, with five animals/group. *Significantly different from untreated control group; asignificantly different from group pretreated with 0.5 g/kg extract.

Figure 3.  A methanol extract of Herba Cistanche affects mitochondrial Ca2+ content in rat hearts. Rats were fed a methanol extract of Herba Cistanche at 0.5 g/kg and 1.0 g/kg for 3 days. Mitochondrial Ca2+ contents were measured as described in “Materials and methods.” Each bar represents mean ± SEM, with five animals/group. *Significantly different from untreated control group; asignificantly different from group pretreated with 0.5 g/kg extract.

Figure 4. A methanol extract of Herba Cistanche affects mitochondrial membrane potential in rat hearts. Rats were fed a methanol extract of Herba Cistanche at 0.5 g/kg and 1.0 g/kg for 3 days. Mitochondrial ΔΨm values were measured as described in “Materials and methods.” Each bar represents mean ± SEM, with five animals/group. *Significantly different from untreated control group.

Figure 4.  A methanol extract of Herba Cistanche affects mitochondrial membrane potential in rat hearts. Rats were fed a methanol extract of Herba Cistanche at 0.5 g/kg and 1.0 g/kg for 3 days. Mitochondrial ΔΨm values were measured as described in “Materials and methods.” Each bar represents mean ± SEM, with five animals/group. *Significantly different from untreated control group.

Table 1. A methanol extract of Herba Cistanche affects mitochondrial respiration in rat hearts.

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