| Literature DB >> 17386115 |
Abstract
Chinese tonifying herbs such as herba cistanche, ganoderma and cordyceps, which possess antioxidant and/or immunomodulatory activities, can be useful in the prevention and treatment of age-related diseases. Pharmacological studies on Yang and Yin tonifying herbs suggest that Yang tonifying herbs stimulate mitochondrial adenosine triphosphate (ATP) generation, presumably through the intermediacy of reactive oxidant species, leading to the enhancement of cellular/mitochondrial antioxidant status. Yin tonifying herbs, however, apart from possessing antioxidant properties, exert mainly immunomodulatory functions that may boost a weak immune system and may also suppress overreactive immune responses. The abilities of Yang and Yin Chinese tonifying herbs to enhance ATP generation and to exhibit antioxidant and/or immunomodulatory actions are the pharmacological basis for their beneficial effects on the retardation of aging.Entities:
Year: 2007 PMID: 17386115 PMCID: PMC1847515 DOI: 10.1186/1749-8546-2-3
Source DB: PubMed Journal: Chin Med ISSN: 1749-8546 Impact factor: 5.455
Effect of Yang and Yin tonifying herbs on myocardial ATP generation capacity in mice ex vivo
| Herbs | ATP generation (% control) | Herbs | ATP generation (% control) |
| Yang herbs | Yin herbs | ||
| | 157 ± 11.2 * | | 95.5 ± 12.1 |
| | 191 ± 3.20 ** | | 101 ± 5.00 |
| | 230 ± 17.3 ** | | 102 ± 4.53 |
| | 149 ± 38.0 | | 98.2 ± 9.92 |
| | 130 ± 7.51 * | | 102 ± 8.51 |
| | 120 ± 19.7 | | 85.0 ± 7.43 |
| | 154 ± 14.6 * | | 82.7 ± 0.92 * |
| | 175 ± 13.4 * | | 80.3 ± 7.05 * |
| | 222 ± 2.12 ** | ||
| | 142 ± 19.3 | ||
| | 133 ± 35.8 |
Mice were pretreated with herbal extracts at daily doses of 1 g/kg for 3 days. The mean value of myocardial ATP generation capacity in unpretreated mice was 147 ± 17.6 (S.D.) nmol ATP/mg protein/10 min, (n = 6). * P < 0.05; ** P < 0.01, Student's t test
Antioxidant and immunomodulatory activities of Chinese tonifying herbs
| aDPPH radical scavenging IC50 (mg/ml) | bImmunomodulatory index | cImmunomodulatory index | |
| Control | 1.00 ± 0.03 | 1.00 ± 0.05 | |
| > 5 | 0.46 ± 0.02* | 1.04 ± 0.09 | |
| 1.0 ± 0.0 | 1.42 ± 0.02* | 1.23 ± 0.01* | |
| 1.8 ± 0.0 | 0.75 ± 0.13 | 0.95 ± 0.12 | |
| 1.1 ± 0.1 | 0.57 ± 0.03* | 0.98 ± 0.01 | |
| 0.8 ± 0.0 | 0.42 ± 0.08* | 1.02 ± 0.02 | |
| > 5 | 2.16 ± 0.10* | 1.31 ± 0.04* | |
| 0.6 ± 0.0 | 0.16 ± 0.03* | 0.97 ± 0.04 | |
| > 5 | 0.59 ± 0.09* | 0.98 ± 0.08 | |
| 0.5 ± 0.0 | 1.73 ± 0.07* | 1.80 ± 0.17* | |
| 1.4 ± 0.1 | 2.54 ± 0.09* | 1.59 ± 0.09* | |
| > 5 | 1.65 ± 0.02* | 1.27 ± 0.12* | |
| > 5 | 0.70 ± 0.02* | 1.24 ± 0.05* | |
| > 5 | 1.65 ± 0.05* | 1.44 ± 0.11* | |
| > 5 | 0.78 ± 0.13 | 0.97 ± 0.04 | |
| 3.5 ± 0.3 | 1.43 ± 0.09* | 1.21 ± 0.06* | |
| > 5 | 1.70 ± 0.03* | 1.39 ± 0.11* |
aMethanol extracts of tonifying herbs were subjected to the DPPH assay. Values given are means ± S.D., (n = 3). (DPPH scavenging activity was regarded as negligible if the IC50 was > 5 mg/ml).
bSplenocytes isolated from mice were cultured in 96-well microtiter plates in a final volume of 100 μl of culture medium, with the respective methanol extracts added at final concentrations ranging from 15.6–1000 μg/ml. Values given are means ± S.E.M., (n = 4).
cAnimals were pretreated orally with the methanol extracts at a daily dose of 1 g/kg for 3 days. All animals were sacrificed 24 hours post-dosing. Splenocytes isolated from pretreated animals were cultured in microtiter plates in a final volume of 100 μl culture medium. Values given are means ± S.E.M., (n = 3–5).
* Significantly different from the control group (P < 0.05)
Nomenclature and classification of selected Yang and Yin tonifying herbs *
| Pharmaceutical name (Chinese | Plant part used | Latin botanical name |
| Bark | ||
| Fruit | ||
| Whole plant | ||
| Whole plant | ||
| Root | ||
| Root | ||
| Rhizome | ||
| Rhizome | ||
| Seed | ||
| Whole plant | ||
| Fruit | ||
| Whole plant | ||
| Whole plant | ||
| Root | ||
| Root | ||
| Root | ||
| Rhizome | ||
| Seed | ||
| Seed | ||
| Fruiting body | ||
| Whole plant |
*Adapted from Liang [17]
Antioxidant activities of Yang tonifying herbs
| HERBS | ANTIOXIDANT ACTIVITIES | REFS |
| water extract caused development of superoxide scavenging activity | [18] | |
| water extract decreased oxidant production in rat osteoblasts | [20] | |
| ethanol extract enhanced blood and liver antioxidant status in rats and mice | [23] | |
| active ingredients (bakuchiol, isobavachin, isobavachalcone) inhibited the NADPH-dependent peroxidation of liver microsomal and mitochondrial lipids | [22] | |
| acetone/water (1:1, v/v) extract caused development of oxygen radical scavenging activity | [16] | |
| water extract caused development of superoxide scavenging activity | [18] | |
| water extract caused development of hydroxyl radical scavenging activity | [19] | |
| ethanol extract increased blood superoxide dismutase and catalase activities in diabetic rats | [24] | |
| acetone/water (1:1, v/v) extract caused development of oxygen radical scavenging activity | [16] |
Immunomodulatory activities of Yin tonifying herbs
| HERBS | IMMUNOMODULATORY ACTIVITIES | REFS |
| Methanolic extract or petroleum ether fraction enhanced Con A-stimulated proliferation of mouse splenocytes | [4,36] | |
| Water extract inhibited TNF-α secretion by suppressing IL-2 secretion from astrocytes | [39] | |
| Water extract inhibited xylene-induced ear swelling and carrageenan-induced paw edema in mice Active ingredients (ruscogenin and ophiopogonin D) decreased zymosan-induced adhesion of HL60 cells to ECV304 cells | [40] | |
| Active ingredients (sesquiterpenes) showed a co-mitogenic effect on Con A and lipopolysaccharide-stimulated mouse splenocytes | [41,42] | |
| Ethanolic extract of black rice (the fruit of | [43] |
Figure 1Anti-aging potential of Chinese tonifying herbs.