Natural Products and some Semi-synthetic Analogues as Potential TRPV1 Ligands for Attenuating Neuropathic Pain

被引:20
|
作者
Naik, Gaurav Gopal [1 ]
Uniyal, Ankit [1 ]
Chouhan, Deepak [1 ]
Tiwari, Vinod [1 ]
Sahu, Alakh N. [1 ]
机构
[1] Indian Inst Technol BHU Varanasi, Dept Pharmaceut Engn & Technol, Varanasi, Uttar Pradesh, India
关键词
TRPV1; channels; neuropathic pain; natural products; semi-synthetic analogues; agonists; antagonists; ROOT GANGLION NEURONS; ION-CHANNEL; VANILLOID; RAT MODEL; ALLYL ISOTHIOCYANATE; CAPSAICIN RECEPTOR; PUNGENT COMPOUNDS; PANAX-GINSENG; BLACK PEPPER; ACTIVATION;
D O I
10.2174/1389201022666210719155931
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Natural products and leads inspired by them have acted as a probe for successful drug discovery for many decades. Pain is an obnoxious sensory and emotional experience associated with potential tissue damage. It affects the quality of life of patients to a greater extent. Despite the availability of several agents targeting TRP receptors, none of them can proficiently alleviate neuropathic pain. TRPV1 is a prospective target for treating neuropathic pain as it is recognized to modulate the pain circuitry at the periphery and the central level. In this review, we have discussed several natural molecules, such as Capsaicinoids, Capsinoids, Piperine, Eugenol, Scutigeral, Ginsenosides, Cinnamaldehyde, Camphor, Shogaol, Gingerols, Zingerone, Allicin, Evodiamine, Allylisothiocyanate, Cannabidiol, Ricinoleic acid, Isovelleral, Capsazepine, Thapsigargin, Pellitorine, Yohimbine, Curcumin and some semi-synthetic analogues that activate TRPV1 channels and consequently, can be further harnessed for the treatment of neuropathic pain.
引用
收藏
页码:766 / 786
页数:21
相关论文
共 12 条
  • [1] Modulation of TRPV1 channel function by natural products in the treatment of pain
    Abbas, Manal Ahmad
    CHEMICO-BIOLOGICAL INTERACTIONS, 2020, 330
  • [2] Unlocking the potential of TRPV1 based siRNA therapeutics for the treatment of chemotherapy-induced neuropathic pain
    Akhilesh
    Uniyal, Ankit
    Gadepalli, Anagha
    Tiwari, Vineeta
    Allani, Meghana
    Chouhan, Deepak
    Ummadisetty, Obulapathi
    Verma, Nimisha
    Tiwari, Vinod
    LIFE SCIENCES, 2022, 288
  • [3] Novel urea and amide TRPV1 antagonists as potential new therapeutic agents for the treatment of neuropathic pain
    Westaway, SM
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2005, 230 : U2501 - U2502
  • [4] Novel dual-target μ-opioid and TRPV1 ligands as potential pharmacotherapeutics for pain management
    Gao, Mengkang
    Zhang, Yang
    Wang, Bingxin
    Guo, Ning
    Shao, Lulian
    Zhai, Weibin
    Jiang, Lei
    Wang, Qiang
    Qian, Hai
    Yan, Lin
    BIOORGANIC CHEMISTRY, 2023, 131
  • [5] Asymmetric synthesis and receptor activity of chiral simplified resiniferatoxin (sRTX) analogues as transient receptor potential vanilloid 1 (TRPV1) ligands
    Kim, Myeong Seop
    Ki, Yooran
    Ahn, Song Yeon
    Yoon, Suyoung
    Kim, Sung-Eun
    Park, Hyeung-Geun
    Sun, Wei
    Son, Karam
    Cui, Minghua
    Choi, Sun
    Pearce, Larry V.
    Esch, Timothy E.
    DeAndrea-Lazarus, Ian A.
    Blumberg, Peter M.
    Lee, Jeewoo
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2014, 24 (01) : 382 - 385
  • [6] Improving the drug-likeness of inspiring natural products - evaluation of the antiparasitic activity against Trypanosoma cruzi through semi-synthetic and simplified analogues of licarin A
    Morais, Thiago R.
    Alves Conserva, Geanne A.
    Varela, Marina T.
    Costa-Silva, Thais A.
    Thevenard, Fernanda
    Ponci, Vitor
    Fortuna, Ana
    Falcao, Amilcar C.
    Tempone, Andre G.
    Fernandes, Joao Paulo S.
    Lago, Joao Henrique G.
    SCIENTIFIC REPORTS, 2020, 10 (01)
  • [7] Improving the drug-likeness of inspiring natural products - evaluation of the antiparasitic activity against Trypanosoma cruzi through semi-synthetic and simplified analogues of licarin A
    Thiago R. Morais
    Geanne A. Alves Conserva
    Marina T. Varela
    Thais A. Costa-Silva
    Fernanda Thevenard
    Vitor Ponci
    Ana Fortuna
    Amílcar C. Falcão
    Andre G. Tempone
    João Paulo S. Fernandes
    João Henrique G. Lago
    Scientific Reports, 10
  • [8] Antinociceptive activity of transient receptor potential channel TRPV1, TRPA1, and TRPM8 antagonists in neurogenic and neuropathic pain models in mice
    Salat, Kinga
    Filipek, Barbara
    JOURNAL OF ZHEJIANG UNIVERSITY-SCIENCE B, 2015, 16 (03): : 167 - 178
  • [9] The potential mechanism of action of gut flora and bile acids through the TGR5/TRPV1 signaling pathway in diabetic peripheral neuropathic pain
    Chen, Peng
    Jiang, Xian
    Fu, Jia
    Ou, Cehua
    Li, Yao
    Jia, Jing
    Liao, Changli
    FRONTIERS IN ENDOCRINOLOGY, 2024, 15
  • [10] Exploring the potential of semi-synthetic Swertiamarin analogues for GLUT facilitation and insulin secretion in NIT-1 cell lines: a molecular docking and in-vitro study
    Kumar, Satyender
    Niguram, Prakash
    Jairaj, Vinod
    Chauhan, Neelam
    Jinagal, Seema
    Sagar, Sneha
    Sindhu, Rakesh Kumar
    Chandra, Amrish
    NATURAL PRODUCT RESEARCH, 2024,