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<p>Therapeutical application of hydrogen sulfide (H<sub>2</sub>S) is limited due to the lack of delivery routes for specific organs and the rapid and wide dispersal of H<sub>2</sub>S in vivo. While H<sub>2</sub>S shows adipogenic effects in vitro, its in vivo impacts on obesity remain unclear. This study applies a H<sub>2</sub>S-slow-releasing hydrogel (H<sub>2</sub>S gel) to deliver H<sub>2</sub>S locally in subcutaneous adipose tissue and examines local lipid accumulation in mice. H<sub>2</sub>S is released from H<sub>2</sub>S gels within 6 h and lasts for 72 h, elevating H<sub>2</sub>S levels in local adipose tissue but not in the plasma. Localized H<sub>2</sub>S gel delivery causes significant lipid accumulation and larger lipid droplet diameter in mouse adipose tissues. The expressions of sterol regulatory element-binding protein, peroxisome proliferator-activated receptor-γ, adiponectin, and perilipin are all upregulated by H<sub>2</sub>S gel injections. Local delivery and retention of H<sub>2</sub>S in adipose tissues increase lipid accumulation more in wild-type than in cystathionine-γ-lyase knockout mice. This study confirms the feasibility of selectively delivering H<sub>2</sub>S via injectable hydrogels and their effectiveness in regulating targeted tissue functions. Furthermore, this work deepens our understanding of the role of H<sub>2</sub>S in obesity development under physiological conditions and offers a practical implementation strategy for H<sub>2</sub>S-based therapeutic interventions.</p>

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Localized delivery and retention of hydrogen sulfide causing regional lipid accumulation in mouse adipose tissues in vivo

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年7月1日

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  • Richa Verma,
  • Ming Fu,
  • Hassan M. Arif,
  • Guangdong Yang,
  • Ishani Sarkar,
  • Kuljeet Kaur,
  • John B. Matson,
  • Lingyun Wu,
  • Rui Wang

摘要

Therapeutical application of hydrogen sulfide (H2S) is limited due to the lack of delivery routes for specific organs and the rapid and wide dispersal of H2S in vivo. While H2S shows adipogenic effects in vitro, its in vivo impacts on obesity remain unclear. This study applies a H2S-slow-releasing hydrogel (H2S gel) to deliver H2S locally in subcutaneous adipose tissue and examines local lipid accumulation in mice. H2S is released from H2S gels within 6 h and lasts for 72 h, elevating H2S levels in local adipose tissue but not in the plasma. Localized H2S gel delivery causes significant lipid accumulation and larger lipid droplet diameter in mouse adipose tissues. The expressions of sterol regulatory element-binding protein, peroxisome proliferator-activated receptor-γ, adiponectin, and perilipin are all upregulated by H2S gel injections. Local delivery and retention of H2S in adipose tissues increase lipid accumulation more in wild-type than in cystathionine-γ-lyase knockout mice. This study confirms the feasibility of selectively delivering H2S via injectable hydrogels and their effectiveness in regulating targeted tissue functions. Furthermore, this work deepens our understanding of the role of H2S in obesity development under physiological conditions and offers a practical implementation strategy for H2S-based therapeutic interventions.