Abstract | BACKGROUND: METHODS: In this study, normal Wistar rats and SIIR rats were randomly divided into two groups: ACA and ACA + EA. To explore the potential mechanisms underlying the glucose-lowering effect, plasma FFA/ insulin and insulin transduction signal pathway proteins were assayed. RESULTS: Combined ACA + EA treatment had a greater glucose-lowering effect than ACA alone in normal Wistar rats (-45% ± 3% vs -19% ± 3%, p < 0.001) and SIIR model rats (-43% ± 2% vs -16% ± 6%, p < 0.001). A significant reduction in plasma FFA levels, improvement in homeostatic model assessment of IR (HOMA-IR) index (-48.9% ± 4.0%, p < 0.001) and insulin sensitivity index (102% ± 16.9%, p < 0.001), and significant increases in insulin receptor substrate 1, glucose transporter 4, and peroxisome proliferator-activated receptor γ protein expressions in skeletal muscle, were also observed in the ACA + EA group of SIIR rats. CONCLUSION: Combined EA and ACA therapy had a greater glucose-lowering effect than ACA monotherapy; this combined therapy could be more effective at improving IR in SIIR rats, which may be related to a reduction in plasma FFA levels and an elevation of insulin signaling proteins. Whether this combined therapy has an effect in type 2 diabetes mellitus (T2DM) patients still needs to be explored.
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Authors | Yuan-Chiang Chung, Ying-I Chen, Chih-Ming Lin, Su-Wei Chang, Tai-Hao Hsu, Wai-Jane Ho, Jaug-Geng Lin, Shih-Liang Chang, Chung-Yuh Tzeng |
Journal | Acupuncture in medicine : journal of the British Medical Acupuncture Society
(Acupunct Med)
Vol. 38
Issue 5
Pg. 335-342
(10 2020)
ISSN: 1759-9873 [Electronic] England |
PMID | 32297559
(Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Glucose Transporter Type 4
- Insulin
- Insulin Receptor Substrate Proteins
- PPAR gamma
- Steroids
- Acarbose
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Topics |
- Acarbose
(administration & dosage)
- Animals
- Combined Modality Therapy
- Electroacupuncture
- Glucose Transporter Type 4
(genetics, metabolism)
- Humans
- Hyperglycemia
(etiology, genetics, metabolism, therapy)
- Insulin
(metabolism)
- Insulin Receptor Substrate Proteins
(genetics, metabolism)
- Insulin Resistance
- Male
- Muscle, Skeletal
(drug effects, metabolism)
- PPAR gamma
(genetics, metabolism)
- Rats
- Rats, Wistar
- Steroids
(adverse effects)
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