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Classification | Diseases | Animals | Sex | Induction | Treatment | Duration | Dosage | Administration | Evaluation | Reference number |
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Antiaging | Vascular senescence | SHRs rats | Male | Genotype | Posttreatment | 14 weeks | 50 mg/kg | Oral gavage daily | SA--gal stain; blood flow assay; p53 and phospho- H2AX determination | [4] |
Senescence | SAMP8 mice | Male | Genotype | Posttreatment | 30 days 70 days | 2, 20, or 50 M | Water ad libitum | SA--gal stain; Morris water maze assay; lifespan assays | [5] |
Senescence | Kunming mice | Male | D-galactose | Posttreatment | 4 weeks 8 weeks | 42, 84, or 168 mg/kg | Oral gavage daily | Morris water maze assay; Klotho expression in cerebrum, heart, kidney, testis, and epididymis tissues | [6] |
Longevity | C. elegans | Male/female | Genotype | Posttreatment | 10 hours | 50 or 100 M | Culture liquid | Lifespan assays | [7] |
Dermal thinning | Kunming mice | Male | Natural aging | Posttreatment | 8 weeks | 18 mg/kg | Oral gavage daily | Dermal layer thickness determination | [51] |
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Atherosclerosis | Atherosclerosis | NZW rabbits | Male | High cholesterol diet | Posttreatment | 12 weeks | 25, 50, or 100 mg/kg | Oral gavage daily | Atherosclerotic plaque area; plasma cholesterol; LDL cholesterol; VLDL cholesterol; plasma triglyceride. | [8] |
Vascular dysfunction | SD rats | Male | Atherogenic-Diet | Posttreatment | 12 weeks | 30, 60, or 120 mg/kg | Oral gavage daily | Vascular reactivity study; eNOS, CRP, IL-6, and TNF- expression | [9, 10] |
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Myocardial ischaemia | Cardiac ischemia-reperfusion | Wistar rats | Male | Occluding left anterior descending coronary artery | Pretreatment | 10 min before reperfusion | 7.5 mg/kg | Intravenous injection | ST segment recovery; myocardial infarct size | [16] |
Cardiac ischemia-reperfusion | C57BL/6J mice | Male | Doxorubicin-induced cardiomyopathy | Posttreatment | 1 week | 10, 30, or 90 mg/kg | Ad libitum | Myocardial mitochondrial biogenesis, improving cardiac function; EPO expression | [17] |
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Cardiovascular organ remodeling | Vascular injury | SD rats | Male | Carotid arterial balloon injury | Posttreatment | 2 weeks | 30, 60, or 120 mg/kg | Oral gavage daily | Carotid neointimal formation; PCNA, a-SMA, PDGF-BB gene expression; VSMCs proliferation and migration. | [14] |
Vascular remodeling and fibrosis | SHR rats | Male | Genotype | Posttreatment | 14 weeks | 50 mg/kg | Oral gavage daily | Intima-media thickness in the aortas, remodeling- related mRNA expressions, and effect on Smad3 deacetylating | [15] |
Cardiac remodeling | SD rats | Male | Pressure-overloaded rats induced by abdominal aortic banding | Posttreatment | 30 days | 30, 60, or 120 mg/kg | Oral gavage daily | Heart weight and left ventricular weight indexes, MMPs, TIMPs, collagens, TGF-β1 protein, ERK1/2, JNK, and p38 activation | [18] |
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Lipid metabolism | Serum cholesterol | SHR rats | Male | Genotype | Posttreatment | 4 weeks | 0.15% THSG in rodent chow | Ad libitum | Cholesterol and neutral lipid content VLDL and HDL fraction | [20] |
Serum cholesterol | SD rats | Male | 20% lard, 10% cholesterol, and 0.2% propylthiouracil | Posttreatment | 1 week | 90, 180 mg/kg | Oral gavage daily | Serum TC, TG, LDL- and HDL-cholesterol levels, and LDL receptor mRNA expression | [21] |
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Learning and memory | β-amyloid peptide- or D-galactose- induced dementia | BALb/c mice | Female | Intracranial injection of 3 L β-amyloid or subcutaneous injection of 50 mg/kg D-galactose for 60 days | Posttreatment | 60 days | 33, 100, or 300 mg/kg | Oral gavage daily | Morris water maze assay; passive avoidance test; MAO-B activity in the cerebral cortex; NGF and NT-3 expression in hippocampal CA1 region | [25, 26] |
Ischemia- reperfusion | Gerbils | Male | Ischemia-reperfusion | Posttreatment | 7 days | 1.5, 3, or 6 mg/kg | Intraperitoneal injection | Morris water maze test | [27] |
Stress; aging; brain damage | C57BL/6J mice | Male | Sleep-deprived; amyloid-β-injected; kainic acid-injected brain damage | Posttreatment | 3 days; 17 days and 24 days; 2 weeks | 50, 100, or 200 mg/kg | Ad libitum | Passive avoidance task; erythropoietin, PGC-1, and haemoglobin expression | [29] |
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Alzheimer’s and Parkinson’s diseases | Alzheimer’s disease | SD rats | Male | Chronic aluminum exposure | Posttreatment | 1, 3, or 5 months | 4 g/kg | Oral gavage daily | Passive avoidance task or Morris water maze tests; APP | [33] |
Alzheimer’s disease | SD rats | Male | Amyloid-β()-injected | Posttreatment | 4 weeks | 25 mg/kg | Oral gavage daily | Passive avoidance task or Morris water maze tests; synaptic structures; Src and NR2B expression | [34] |
Alzheimer’s disease | APP Tg mice | Male | APPV717I Tg mice | Posttreatment | 6 months | 120 or 240 mol/kg/d | Oral gavage daily | -synuclein expression and aggregation in the hippocampus | [35] |
Parkinson’s disease | C57BL/6 mice | Male | MPP+-induced damage | Posttreatment | 14 days | 20 or 40 mg/kg | Oral gavage daily | Pole test; tyrosine hydroxylase-positive neurons in the substantia nigral compacts | [36] |
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Cerebral ischemia | Cerebral ischemia | SD rats | Male | Middle cerebral artery occlusion | Posttreatment | 7 days prior to surgery | 30, 60, or 120 mg/kg | Oral gavage daily | Percentage of apoptotic cells in injured rat brain tissue; Bcl-2 and Bax protein expression in brain tissue | [40] |
Cerebral ischemia | SD rats | Male | Middle cerebral artery occlusion | Posttreatment | 7 days prior to surgery | 60 or 120 mg/kg | Oral gavage daily | Animal’s nerve behavior and neurological function score; expression of NGF, GAP-43, and PKA catalytic subunit proteins. | [41] |
Cerebral ischemia | Mice | Male | Middle cerebral artery occlusion | Posttreatment | At the onset of reperfusion | 15 or 40 mg/kg | Intraperitoneal administration | The brain infarct volume and the number of positive cells | [42] |
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Diabetes | Diabetic nephropathy | SD rats | Male | 60 mg/kg streptozotocin intraperitoneal injection | Posttreatment | 8 weeks | 10 or 20 mg/kg | Treatment with TSG | Blood urea nitrogen, creatinine, 24 h urinary protein, ratio of kidney weight/body weight, SOD and GSH-Px activities, and TGF-β1 and COX-2 expression. | [43] |
Diabetic gastrointestinal dysmotility | Kunming mice | Male | 150 mg/kg streptozotocin intraperitoneal injection | Posttreatment | 8 weeks | 10, 30, or 60 mg/kg | Oral gavage daily | Gastric emptying, intestinal transit, and NANC relaxations | [44] |
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Bone | Bone mineral density and bone strength | SD rats | Male and female | Natural development (110 ± 10 g) | Posttreatment | 90 days | 150, 300, or 600 mg/kg | Oral gavage daily | Bone mineral density and bone strength; bone mineral weight and bone mineral size | [45] |
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Hair | Hair growth | C57BL/6J mice | Female | Natural development (20–26 g) | Posttreatment | 9, 18 days | 50, 100, or 150 mg/kg | Oral gavage daily | Hair follicles and capillary growth | [47] |
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