# Mechanisms of Enteroendocrine L-Cell Dysfunction and Bile Adaptations to Weight Loss

> **NIH NIH K23** · MAYO CLINIC ROCHESTER · 2021 · $195,931

## Abstract

ABSTRACT
In this Mentored Career Development Award (K23) proposal, this candidate proposes to solidify a basic
science foundation and clinical research acquired during his PhD and post-doctoral work with a long-term goal
of becoming an academic authority in enteroendocrine L-cell regulation of satiety in obesity. The candidate
aims to acquire a strong foundation in clinical translation science and to acquire a set of novel complementary
skills necessary for an independent research career in gastrointestinal regulation of food intake.
Understanding pathophysiology of human obesity is limited by the heterogeneity of patients' phenotype and
multiple etiological mechanisms. These factors contribute to the highly variable inter-individual weight loss
response to all interventions. Recently, we identified a sub-population of obesity with significantly decreased
satiety (defined as lack of sensation of feeling full or rapid return of hunger). Our preliminary data shows that,
in addition to decreased perception of fullness after a meal, these individuals, compared to other obesity
phenotypes, have very low postprandial levels of the GI satiety hormones GLP-1 and PYY which are secreted
by enteroendocrine (EE) L-cells. The low levels of the satiety hormone PYY and possibly other EE cell
products suggests that the increased calorie intake originates from a deficit in the gut hormones, and this
phenotype is summarized as a “hungry gut”. The suboptimal EE cell function, which could be mediated by
altered synthesis or secretion by the EE cells themselves, or a decrease in luminal concentrations of molecules
that normally stimulate EE cells, such as amino acids, bile acids, or short-chain fatty acids. Our preliminary
results also suggest that these individuals have lower levels of FGF-19, a surrogate of the luminal bile acid
concentration.
Based on these preliminary studies, it is essential to understand the mechanisms that are responsible for
the deficient EE signals that lead to the “hungry gut” phenotype of obesity. To test this concept, we
propose the following two aims: 1) to study the mechanism of the hungry gut phenotype down to the level of
the EE cells, and compare these findings to other obesity phenotypes and normal weight, healthy controls. 2)
To restore normal satiety by increasing enteroendocrine cell function and secretion in patients after Roux-in-y
gastric bypass surgery or in response to treatment with luminal bile acids. These findings will provide the
foundation for further studies of the “hungry gut” phenotype in a future R01 application. This work will be
performed in an academically nurturing environment within Mayo Clinic and with full support of the Division of
Gastroenterology. The candidate will be guided by a strong mentorship committee (Drs. Michael Camilleri,
Nicholas LaRusso and Adrian Vella). As a result of this work, the candidate will significantly advance our
understanding of EE cell function in human obesity and develop his c...

## Key facts

- **NIH application ID:** 10137913
- **Project number:** 5K23DK114460-04
- **Recipient organization:** MAYO CLINIC ROCHESTER
- **Principal Investigator:** Andres J Acosta
- **Activity code:** K23 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2021
- **Award amount:** $195,931
- **Award type:** 5
- **Project period:** 2018-08-01 → 2023-04-30

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10137913

## Citation

> US National Institutes of Health, RePORTER application 10137913, Mechanisms of Enteroendocrine L-Cell Dysfunction and Bile Adaptations to Weight Loss (5K23DK114460-04). Retrieved via AI Analytics 2026-05-24 from https://api.ai-analytics.org/grant/nih/10137913. Licensed CC0.

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