DACRA induces profound weight loss, satiety control, and increased mitochondrial respiratory capacity in adipose tissue
- PMID: 38879729
- DOI: 10.1038/s41366-024-01564-w
DACRA induces profound weight loss, satiety control, and increased mitochondrial respiratory capacity in adipose tissue
Abstract
Background and objectives: Dual amylin and calcitonin receptor agonists (DACRAs) are therapeutic candidates in the treatment of obesity with beneficial effects on weight loss superior to suppression of food intake. Hence, suggesting effects on energy expenditure by possibly targeting mitochondria in metabolically active tissue.
Methods: Male rats with HFD-induced obesity received a DACRA, KBP-336, every third day for 8 weeks. Upon study end, mitochondrial respiratory capacity (MRC), - enzyme activity, - transcriptional factors, and -content were measured in perirenal (pAT) and inguinal adipose tissue. A pair-fed group was included to examine food intake-independent effects of KBP-336.
Results: A vehicle-corrected weight loss (23.4 ± 2.8%) was achieved with KBP-336, which was not observed to the same extent with the food-restricted weight loss (12.4 ± 2.8%) (P < 0.001). Maximal coupled respiration supported by carbohydrate and lipid-linked substrates was increased after KBP-336 treatment independent of food intake in pAT (P < 0.01). Moreover, oligomycin-induced leak respiration and the activity of citrate synthase and β-hydroxyacetyl-CoA-dehydrogenase were increased with KBP-336 treatment (P < 0.05). These effects occurred without changes in mitochondrial content in pAT.
Conclusions: These findings demonstrate favorable effects of KBP-336 on MRC in adipose tissue, indicating an increased energy expenditure and capacity to utilize fatty acids. Thus, providing more mechanistic insight into the DACRA-induced weight loss.
© 2024. The Author(s), under exclusive licence to Springer Nature Limited.
Similar articles
-
Optimization of tolerability and efficacy of the novel dual amylin and calcitonin receptor agonist KBP-089 through dose escalation and combination with a GLP-1 analog.Am J Physiol Endocrinol Metab. 2017 Nov 1;313(5):E598-E607. doi: 10.1152/ajpendo.00419.2016. Epub 2017 Mar 14. Am J Physiol Endocrinol Metab. 2017. PMID: 28292761
-
A novel dual amylin and calcitonin receptor agonist, KBP-089, induces weight loss through a reduction in fat, but not lean mass, while improving food preference.Br J Pharmacol. 2017 Apr;174(7):591-602. doi: 10.1111/bph.13723. Epub 2017 Feb 15. Br J Pharmacol. 2017. PMID: 28109166 Free PMC article.
-
Dose Frequency Optimization of the Dual Amylin and Calcitonin Receptor Agonist KBP-088: Long-Lasting Improvement in Food Preference and Body Weight Loss.J Pharmacol Exp Ther. 2020 May;373(2):269-278. doi: 10.1124/jpet.119.263400. Epub 2020 Feb 18. J Pharmacol Exp Ther. 2020. PMID: 32071103
-
Amylin and Calcitonin: Potential Therapeutic Strategies to Reduce Body Weight and Liver Fat.Front Endocrinol (Lausanne). 2021 Jan 8;11:617400. doi: 10.3389/fendo.2020.617400. eCollection 2020. Front Endocrinol (Lausanne). 2021. PMID: 33488526 Free PMC article. Review.
-
Central control of energy balance by amylin and calcitonin receptor agonists and their potential for treatment of metabolic diseases.Basic Clin Pharmacol Toxicol. 2020 Sep;127(3):163-177. doi: 10.1111/bcpt.13427. Epub 2020 May 18. Basic Clin Pharmacol Toxicol. 2020. PMID: 32363722 Review.
Cited by
-
Exogenous oral application of PYY and exendin-4 impacts upon taste-related behavior and taste perception in wild-type mice.Neuropharmacology. 2025 Jul 1;272:110408. doi: 10.1016/j.neuropharm.2025.110408. Epub 2025 Mar 12. Neuropharmacology. 2025. PMID: 40086622
References
-
- Wharton S, Lau DCW, Vallis M, Sharma AM, Biertho L, Campbell-Scherer D, et al. Obesity in adults: a clinical practice guideline. C. Can Med Assoc J. 2020;192:E875–91. - DOI
-
- Mathiesen DS, Lund A, Vilsbøll T, Knop FK, Bagger JI. Amylin and Calcitonin: Potential Therapeutic Strategies to Reduce Body Weight and Liver Fat. Front Endocrinol. 2020;11:617400. - DOI
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical