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GRK-Biased Activation Via β2-Adrenergic Receptors in Human Skeletal Muscle (GAIN)

2026年10月8日 更新者:Morten Hostrup, PhD

G Protein-Coupled Receptor Kinase (GRK)-Biased Signaling Via β2-Adrenergic Receptors and Downstream Activation and Its Role for Protein Synthesis-Regulating Kinases, Function and Receptor Desensitization in Human Skeletal Muscle

This longitudinal mechanistic physiological study examines biased β2-adrenergic receptor (β2-AR) signaling in human skeletal muscle, with emphasis on G protein-coupled receptor kinase (GRK)-mediated pathways. Participants will receive daily oral dosing of the GRK-selective long-acting β2-agonist ATR-258 for 8 weeks. Muscle biopsies and physiological measurements will quantify GRK-, cAMP/PKA-, and β-arrestin-related up- and downstream signaling, fiber-type specificity, and potential receptor desensitization with repeated stimulation along with functional read-outs, tissue distribution, cardiovascular response and tolerability.

研究概览

地位

主动,不招人

干预/治疗

详细说明

Healthy men with overweight/obesity will complete an 8-week intervention with daily oral ATR-258 (0.5-2.5 mg/day). On experimental days (Days 1, 15, 29, and 56), β2-AR signaling sensitivity will be assessed before and after stimulation (1-2, 4, and 8 hours) using blood biomarkers, hemodynamics, indirect calorimetry, and lower extremity muscle function/power testing. Muscle biopsies (vastus lateralis) will be obtained at rest and 4 hours after stimulation on Days 1, 29, and 56 to quantify downstream signaling (GRK, cAMP/PKA, β-arrestin), phosphorylation of rpS6/mTOR/Akt, β2-AR content, and muscle fiber morphology.

研究类型

介入性

注册 (实际的)

13

阶段

  • 阶段2

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Copenhagen、丹麦、2100
        • University of Copenhagen, August Krogh Section for Human & Molecular Physiology

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

21年 至 45年 (成人)

接受健康志愿者

是的

有资格学习的性别

男性

描述

Inclusion Criteria:

  • Healthy men
  • Age 21-45 years
  • BMI 25-35 kg/m^2
  • Body fat percentage 25-40%
  • Lean Mass Index 14-22

Exclusion Criteria:

  • Regular use of or allergy to β2-agonists
  • Serious adverse reactions to β2-agonists
  • Current smoker
  • Regular use of medication (except OTC allergy or analgesics)
  • Abnormal ECG before or after β2-AR stimulation
  • Hypertension
  • Reduced kidney function (eGFR < 90 ml/min/1.73m^2)
  • Cardiovascular, metabolic, gastrointestinal, renal, or pulmonary disease
  • Psychiatric or neurological disorders affecting compliance/safety reporting
  • Cancer history within the last 5 years
  • Substance abuse or alcohol intake >14 units/week

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:基础科学
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:ATR-258

Daily oral ATR-258

Daily oral ATR-258 for 8 weeks with repeated experimental assessment days (Days 1, 15, 29, 56).

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Intensity of β2-AR downstream signaling pathways (e.g. GRK, cAMP/PKA, β-arrestin, rpS6) in type I and type II muscle fibers
大体时间:Before and 4 hours after ATR-258 ingestion on day 1, 29, and 56.

Assessed in vastus lateralis biopsies at rest

Before and 4 hours after ATR-258 ingestion on day 1, 29, and 56.

次要结果测量

结果测量
措施说明
大体时间
Phosphorylation of rpS6, mTOR, and Akt in type I and type II muscle fibers
大体时间:Day 1, 29 and, 56.

In response to ATR-258 ingestion

Day 1, 29 and, 56.
Lean/fat mass
大体时间:Day 1, 15, 29, and 56

Measured by DXA scan

Day 1, 15, 29, and 56
Muscle function
大体时间:Pre and post 8 weeks of daily ATR-258 ingestion. Post visit conducted 2-5 days after last day of ATR-258 ingestion.

Participants will perform lower extremity peak exercise and a one-legged knee-extensor exercise protocol to exhaustion before and after the full intervention to assess muscle power and endurance

Pre and post 8 weeks of daily ATR-258 ingestion. Post visit conducted 2-5 days after last day of ATR-258 ingestion.
Peripheral glucose clearance including OGTT-derived outcomes
大体时间:Pre and post 8 weeks of daily ATR-258 ingestion. Post visit conducted 2-5 days after last day of ATR-258 ingestion.
Pre and post 8 weeks of daily ATR-258 ingestion. Post visit conducted 2-5 days after last day of ATR-258 ingestion.
β2-adrenergic receptor content in type I and type II muscle fibers
大体时间:On day 1, 29 and 56

Measured by western blotting

On day 1, 29 and 56
Resting metabolic rate (incl. carbohydrate and fat oxidation)
大体时间:Before and 1, 2, 4 and 8 hours after ATR-258 ingestion on day 1, 15, 29, and 56.

Measured by indirect calorimetry

Before and 1, 2, 4 and 8 hours after ATR-258 ingestion on day 1, 15, 29, and 56.
Femoral arterial blood flow
大体时间:Before and 1, 2, 4 and 8 hours after ATR-258 ingestion on day 1, 15, 29, and 56.

Measured by Doppler.

Before and 1, 2, 4 and 8 hours after ATR-258 ingestion on day 1, 15, 29, and 56.
Continous ECG and heart rate
大体时间:A 5-day baseline period, and day 1-5, day 15-20, and day 29-34 of ATR-258 administration.

Participants will wear a Holter-device for 4 x 5 days to continuously measure ECG and heart rate. The periods will be after the screening (baseline period), and after trial days on Day 1, 15, and 29.

A 5-day baseline period, and day 1-5, day 15-20, and day 29-34 of ATR-258 administration.
Muscle fiber cross-sectional area (type I and type II)
大体时间:Day 1, 29, and 56

Measured by histochemical analysis

Day 1, 29, and 56
Maximal electrically-stimulated muscle force development and relaxation
大体时间:Pre and post 8 weeks of daily ATR-258 ingestion. Post visit conducted 2-5 days after last day of ATR-258 ingestion.

Isometric quadriceps. Measured seated with leg in 90 degree angle and attached to strain gauge.

Pre and post 8 weeks of daily ATR-258 ingestion. Post visit conducted 2-5 days after last day of ATR-258 ingestion.

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2026年2月19日

初级完成 (估计的)

2026年12月31日

研究完成 (估计的)

2026年12月31日

研究注册日期

首次提交

2026年1月30日

首先提交符合 QC 标准的

2026年2月16日

首次发布 (实际的)

2026年2月19日

研究记录更新

最后更新发布 (实际的)

2026年10月14日

上次提交的符合 QC 标准的更新

2026年10月8日

最后验证

2026年10月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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