Key result
In insulin-resistant mice, betatrophin expression and serum levels were significantly increased (p=0.000), while citrate synthase gene expression was decreased (p=0.01).
Why the study?
The study sought to examine the relationship of betatrophin with key metabolic enzymes, namely LDH5, CS, and ACC1, in insulin-resistant mice.
In insulin-resistant mice, betatrophin levels are elevated and correlate with triglycerides, but betatrophin does not appear to directly regulate carbohydrate or lipid metabolism through CS, LDH5, or ACC1 enzymes.
Answers are grounded in this paper and cite their sources.
Betatrophin elevation without metabolic enzyme correlation in mice is hypothesis-generating; leaves open pathways and precludes clinical translation.
OBJECTIVES: The present study sought to examine the relationship of betatrophin with certain key enzymes, namely lactate dehydrogenase-5 (LDH5), citrate synthase (CS), and acetyl-CoA carboxylase-1 (ACC1), in insulin-resistant mice. METHODS: Eight-week-old male C57BL6/J mice were used in this study (experimental group n=10 and control group n=10). S961 was administered using an osmotic pump to induce insulin resistance in the mice. The betatrophin, LDH5, CS, and ACC1 expression levels were determined from the livers of the mice using the real-time polymerase chain reaction (RT-PCR) method. Moreover, biochemical parameters such as the serum betatrophin, fasting glucose, insulin, triglyceride, total cholesterol, and high-density lipoprotein (HDL) and low-density lipoprotein (LDL) cholesterol levels were analyzed. RESULTS: The betatrophin expression and serum betatrophin (p=0.000), fasting glucose, insulin, triglyceride (p≤0.001), and total cholesterol (p=0.013) levels were increased in the experimental group. In addition, the CS gene expression level was statistically significantly decreased in the experimental group (p=0.01). Although strong correlation was found between the expression and serum betatrophin and triglyceride levels, no correlation was found between the betatrophin gene expression and the LDH5, ACC1, and CS gene expression levels. CONCLUSIONS: The betatrophin level appears to play an important role in the regulation of triglyceride metabolism, while insulin resistance increases both the betatrophin gene expression and serum levels and decreases the CS expression level. The findings suggest that betatrophin may not regulate carbohydrate metabolism through CS and LDH5 or lipid metabolism directly through the ACC1 enzyme.
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Arıkan et al. (2023) studied Insulin resistance (n=20). S961 vs. control group was evaluated on Betatrophin, LDH5, CS, and ACC1 expression levels and biochemical parameters (p=0.000). In insulin-resistant mice, betatrophin expression and serum levels were significantly increased (p=0.000), while citrate synthase gene expression was decreased (p=0.01).
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