日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Recommended Opioid Receptor Tool Compounds: Comparative In Vitro for Receptor Selectivity Profiles and In Vivo for Pharmacological Antinociceptive Profiles

推荐的阿片受体工具化合物:体外受体选择性比较和体内药理镇痛特性比较

Tran, Linh T; Freeman, Katie T; Lunzer, Mary M; Portoghese, Philip S; Haskell-Luevano, Carrie

Incorporation of Three Extracyclic Arginine Residues into a Melanocortin Macrocyclic Agonist (c[Pro-His-DPhe-Arg-Trp-Dap-Lys(Arg-Arg-Arg-Ac)-DPro]) Decreases Food Intake When Administered Intrathecally or Subcutaneously Compared to a Macrocyclic Ligand Lacking Extracyclic Arginine Residues (c[Pro-His-DPhe-Arg-Trp-Dap-Ala-DPro)]

将三个环外精氨酸残基掺入黑皮质素大环激动剂(c[Pro-His-DPhe-Arg-Trp-Dap-Lys(Arg-Arg-Arg-Ac)-DPro])中,与缺乏环外精氨酸残基的大环配体(c[Pro-His-DPhe-Arg-Trp-Dap-Ala-DPro])相比,鞘内或皮下注射该激动剂可降低食物摄入量。

Ericson, Mark D; Freeman, Katie T; Larson, Courtney M; Bouchard, Jacob L; John, Kristen; Lunzer, Mary M; Koerperich, Zoe M; Haskell-Luevano, Carrie

MMG22 Potently Blocks Hyperalgesia in Cisplatin-treated Mice

MMG22 能有效阻断顺铂治疗小鼠的痛觉过敏

Cataldo, Giuseppe; Lunzer, Mary M; Akgün, Eyup; Wong, Henry L; Portoghese, Philip S; Simone, Donald A

The bivalent ligand, MMG22, reduces neuropathic pain after nerve injury without the side effects of traditional opioids

二价配体MMG22可减轻神经损伤后的神经性疼痛,且无传统阿片类药物的副作用。

Speltz, Rebecca; Lunzer, Mary M; Shueb, Sarah S; Akgün, Eyup; Reed, Rachelle; Kalyuzhny, Alex; Portoghese, Philip S; Simone, Donald A

The bivalent ligand MCC22 potently attenuates hyperalgesia in a mouse model of cisplatin-evoked neuropathic pain without tolerance or reward

二价配体MCC22能有效减轻顺铂诱导的小鼠神经性疼痛模型中的痛觉过敏,且不产生耐受性或奖赏效应。

Cataldo, Giuseppe; Erb, Samuel J; Lunzer, Mary M; Luong, Nhungoc; Akgün, Eyup; Portoghese, Philip S; Olson, Julie K; Simone, Donald A

Targeting MOR-mGluR(5) heteromers reduces bone cancer pain by activating MOR and inhibiting mGluR5

靶向 MOR-mGluR(5) 异源二聚体可通过激活 MOR 和抑制 mGluR5 来减轻骨癌疼痛。

Shueb, Sarah S; Erb, Samuel J; Lunzer, Mary M; Speltz, Rebecca; Harding-Rose, Catherine; Akgün, Eyup; Simone, Donald A; Portoghese, Philip S

Bivalent ligand MCC22 potently attenuates nociception in a murine model of sickle cell disease

二价配体MCC22能有效减弱镰状细胞病小鼠模型中的伤害感受。

Cataldo, Giuseppe; Lunzer, Mary M; Olson, Julie K; Akgün, Eyup; Belcher, John D; Vercellotti, Gregory M; Portoghese, Philip S; Simone, Donald A

Bivalent ligand that activates mu opioid receptor and antagonizes mGluR5 receptor reduces neuropathic pain in mice

一种能激活μ阿片受体并拮抗mGluR5受体的二价配体可减轻小鼠的神经性疼痛。

Peterson, Cristina D; Kitto, Kelley F; Akgün, Eyup; Lunzer, Mary M; Riedl, Maureen S; Vulchanova, Lucy; Wilcox, George L; Portoghese, Philip S; Fairbanks, Carolyn A

Putative kappa opioid heteromers as targets for developing analgesics free of adverse effects.

假定的 kappa 阿片类异聚体是开发无不良反应镇痛药的目标

Le Naour Morgan, Lunzer Mary M, Powers Michael D, Kalyuzhny Alexander E, Benneyworth Michael A, Thomas Mark J, Portoghese Philip S

Ligands that interact with putative MOR-mGluR5 heteromer in mice with inflammatory pain produce potent antinociception

在患有炎症性疼痛的小鼠中,与假定的 MOR-mGluR5 异源二聚体相互作用的配体可产生强效镇痛作用。

Akgün, Eyup; Javed, Muhammad I; Lunzer, Mary M; Smeester, Branden A; Beitz, Al J; Portoghese, Philip S