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Article Commentary

Transient Receptor Potential channels: A Global Bibliometric analysis From 2012 to 2021

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Pages 624-634 | Received 23 Aug 2021, Accepted 14 Sep 2021, Published online: 13 Nov 2021

Introduction

The transient receptor potential (TRP) channels, nonselective ion channels, mediate the fluxes of various types of cations across the cell membrane such as Na+, K+, Mg2+, and Ca2 + . TRPA (Ankyrin), TRPC (Canonical), TRPM (Melastatin), TRPV (Vanilloid), TRPP (Polycystin), and TRPML (Mucolipin) are TRP major families members.

These channels play essential roles in diverse physiologic processes, and participate in virtually every sensory modality. TRPs can be activated by chemicals, temperature, stretch/pressure, osmolarity, pH, and so on, and play a major role in the five primary senses, such as vision, taste, hearing, smell, and touch. In recent years, TRP channels are widely studied in the field of nervous, intestinal, renal, urogenital, respiratory, and cardiovascular systems in diverse therapeutic areas including pain and itch, headache, pulmonary function, oncology, neurology, visceral organs, and genetic diseases [Citation1].

Bibliometric analysis has been widely used to calculate the productivity of countries, institutions, authors, and the frequency of keywords to explore research hotspots/frontiers in specific fields [Citation2–4]. In the present study, we performed a bibliometric analysis to systematically evaluate the TRP channels studies from 2012 to 2021 by CiteSpace and VOSviewer to provide researchers with some direction regarding TRP channels research [Citation5,Citation6].

Data source and search

The publications were obtained from the Core Collection database of Web of Science (WoS) (http://apps.webofknowledge.com) which is considered the most prominent database of scientific publications on many research topics. The data search was conducted on 10 July 2021. The strategy used during the search was [TS = transient receptor potential channel * OR transient receptor potential * OR TRP channel* OR TRP*] AND [Language = (English)] AND [Year Range = (2012–2021)]. 34,278 publications were obtained, and the following documents were excluded: meeting abstract(3,153) proceedings paper(603) editorial material(380) early access(241) book chapter(188) letter(130) correction(126) news item(15) data paper(14) petracted publication(9) retraction(6) record reciew(3) reprint(2) book review(1) poetry(1). In total, only 29,406 records (26,767 articles and 2,639 reviews) were analyzed. The data were collected within 1 day to avoid any potential deviation due to the daily updating of the database. The VOSviewer 1.6.16 was used to identify top countries, institutions, authors, and journals. The CiteSpace 5.8. R1 was used to analyze keywords, co-cited references, and trends. The data analysis flow chart is shown in (). In this study, the data were downloaded directly from the database as secondary data without further animal experiments. Therefore, no ethical approval was required.

Figure 1. Flow chart for the analysis of TRP channels researches

Figure 1. Flow chart for the analysis of TRP channels researches

Annual publication output

A total of 29,406 TRP-related publications were obtained. To explore the trends in TRP channel research, we showed the number of articles per year in the form of a histogram. Because the annual number of published papers reflects the pace of subject knowledge and is a significant indicator for studying the trends in the field [Citation7]. As shown in (), the annual number of relevant publications started increasing rapidly from 2012 to 2021, indicating a steady development and more attention of TRP. And up to 10 July 2021, more than 1,967 literature have been published in 2021. Furthermore, articles account for about 91.03% in terms of document type (), which indicates the greater emphasis paid on original studies in the area of TRP.

Figure 2. The number of annual publications on TRP channels research from 2012 to 2021

Figure 2. The number of annual publications on TRP channels research from 2012 to 2021

Figure 3. Document type. Blue represents articles and Orange represents reviews

Figure 3. Document type. Blue represents articles and Orange represents reviews

Active countries and institutions

Geographical distribution map of global productivity revealed that articles on TRP channels had been mainly published from North American, Asia, and European countries (). () lists the top 10 countries and institutions ranked by the numbers of publications on the TRP channels. The 29,406 literature were published by more than 16,103 research institutions in 132 countries/territories. The co-occurrence map provides valuable information on influential research teams and helps researchers to identify the cooperative relationship [Citation8–10]. Countries and institutions co-occurrence maps are shown in () and 6. The leading country was the USA, which took up 30.11% (8853/29,406) of the total number of publications, followed by CHINA (6259, 21.285%) and JAPAN (2706, 9.202%). () shows that the United States attached great importance to cooperation, and had close collaborations with China, Japan, and Germany. The most productive scientific research institution was the Chinese Academy of Sciences, produced the highest number of publications on TRP channels (525), followed by Seoul National University (284). As shown in (), the collaboration map had 500 nodes and 12,343 links. The 500 institutions formed nine clusters with different colors. The co-occurrence map of institutions showed that scientific cooperation among institutions was greatly affected by the geographical location, and there are more cooperations among institutions in the same region ().

Table 1. The top 10 countries and institutions contributed to publications on TRP channels research

Figure 4. Geographical distribution map of global publications related to TRP channels

Figure 4. Geographical distribution map of global publications related to TRP channels

Figure 5. The network of countries/territories engaged in TRP channels research

Figure 5. The network of countries/territories engaged in TRP channels research

Figure 6. The network of institutions engaged in TRPs channel research

Figure 6. The network of institutions engaged in TRPs channel research

Active journals

The 29,406 literature were published in 3,992 journals. () lists the top 10 journals that published articles on TRP channels research. The Plos One had the highest number at 766 (2.61%) (IF2020 = 3.24), followed by Science Reports published 590 papers (2.01%) (IF2020 = 4.379, and the Journal of Biological Chemistry ranked third at 447 articles (1.52%) (IF2020 = 5.157).

Table 2. The top 10 journals that published articles on TRP channels research

Active authors

Author co-occurrence map can provide information on influential research groups and potential collaborators. It can help researchers to find potential collaborators [Citation8,Citation9]. A total of approximately 100,000 authors were obtained in the 29,406 publications elated to TRP channels research. The networks shown in () indicate the cooperation among authors, and the top10 active authors are listed in (). Tominaga, Makoto, mainly focused on The Role of TRP Channels in Thermosensation and Nociception [Citation11,Citation12], contributed the most papers (118 publications, 0.40%), followed by Birnbaumer, Lutz and Mori, Yasuo with 96 and 76 publications, respectively. There was an active collaboration among the productive authors.

Table 3. The top10 active authors in TRP channels research

Figure 7. The network of authors contributed to TRP channels research

Figure 7. The network of authors contributed to TRP channels research

Co-cited references

29,406 publications were visualized and analyzed using CiteSpace 5.8.R1 with a period time from 2012 to 2021, and a time slice of 1 was chosen for the analysis of the co-cited references. The network of co-cited references on TRP channels consists of references with higher centrality and citation counts which is presented in (). The highly cited references were analyzed to determine the key knowledge base in the field. The top 10 highest co-cited references are summarized in (). These articles laid the foundation for studying the structure and mechanism of TRP channels. And these reviews provided a theoretical basis for the study of TRP channels.

Table 4. The top10 Co-cited references in TRP channels research

Figure 8. The analysis of Co-cited references: Co-citation network of references from publications on TRP channels research

Figure 8. The analysis of Co-cited references: Co-citation network of references from publications on TRP channels research

The first highly co-cited article was “Structure of the TRPV1 ion channel determined by electron cryo-microscopy.” (476 citation rate), in which Maofu Liao explored advances in electron cryo-microscopy to determine the structure of TRPV1, at 3.4 Å resolution and provided a structural blueprint for understanding unique aspects of TRP channel function [Citation13]. There were other three co-cited references published in Nature: In 2013, Erhu Cao revealed that TRPV1 opening was associated with structural rearrangements in the outer pore, and suggested a dual gating mechanism [Citation14]. In 2015, Candice E Paulsen used single-particle electron cryo-microscopy to determine the structure of full-length TRPA1 to ∼4 Å resolution in the presence of pharmacophores, including a potent antagonist [Citation15]. One year later, Yuan Gao demonstrated the power of combining electron cryo-microscopy with lipid nanodisc technology to ascertain the structure of the rat TRPV1 ion channel in a native bilayer environment [Citation16].

Research area analysis

() shows the top 15 research areas that appeared in publications related to TRP channels research from 2012 to 2021. BIOCHEMISTRY MOLECULAR BIOLOGY, CHEMISTRY, and PHARMACOLOGY PHARMACY are the top three areas where TRP channels are more studied.

Figure 9. The 15 research areas on TRP channels research

Figure 9. The 15 research areas on TRP channels research

Keyword co-occurrence

Keywords were extracted from titles and abstracts of all the 19,406 publications, which is the crucial content of research. Keyword co-occurrence analysis provides a reasonable description of research hotspots, and burst keywords can represent research frontiers over a period of time [Citation17].

CiteSpace 5.8.R1 was used to construct an acknowledge map of keyword co-occurrence () and identified the top 20 keywords in TRP channels research from 2012 to 2021(), according to frequency. The top keywords were “expression,” “activation,” “protein,” “mechanism,” “receptor,” “ion channel,” “trpv1,” “channel,” “pain,” “cell,” “calcium,” “inflammation,” “identification,” “trp channel,” “inhibition,” “tryptophan,” “gene,” “rat,” “binding,” “oxidative stress.” Therefore, research hotspots can be summarized in the following aspects

Table 5. Top 20 keywords in terms of frequency in nTRP channels research

Figure 10. The analysis of keywords inTRP channels research

Figure 10. The analysis of keywords inTRP channels research

① TRPV1

TRPV1 channel involves the regulation of many important physiological and pathological processes. In many diseases, the TRPV1 channel may be an effective treatment in the future, such as inflammation, cardiovascular disease, pain, diabetes, schizophrenia, pneumonia, psoriasis, and so on.

a) TRPV1 and inflammation: TRPV1 is closely associated with inflammation and is responsible for the neurogenic component of inflammation development, which is large expressed in nociceptive neurons of the peripheral nervous system [Citation18]. Activation of TRPV1 channels can release neuropeptides from nerve endings and simultaneously increase vascular permeability. Research shows that the vascular permeability in the respiratory tract inflammation model increased after microinjection of the TRPV1 agonist and decreased after microinjection of the TRPV1 antagonist [Citation19]. Fibroblasts are originally TRPV1 negative cells, and after stimulating by proinflammatory agents, such as TNF-α, IL-1α, and LPS cells for 24 and 48 hours, fibroblasts begin to synthesize TRPV1 mRNA, which confirming the functionality of the membrane-embedded receptors [Citation20].

b) TRPV1 and cardiovascular disease: TRPV1 is highly expressed in the smooth muscles of coronary arterioles, skeletal muscles, adipose tissue, and microvessels (vasa vasorum) [Citation21]. It was found that TRPV causes the Bezold–Jarisch cardiopulmonary chemical reflex manifested in a short-term drop in BP, bradycardia, and apnea [Citation22], and the transient Bezold–Jarisch reflex is mediated by the TRPV1 activation in the sensory neurons, while TRPV1 activation in arterioles induces the BP increase [Citation21]. TRPV1 also affects circulation through the spinal cord neurons and DRG neurons. The experiment shows that on the myocardial ischemia-reperfusion, additional activation of the spinal cord TRPV1 contributed to a severer myocardial injury; however, intrathecal administration of the TRPV1 antagonist capsazepine reduced the size of the infarct area [Citation23].

②- TRP channels and pain

Pain can be divided into three categories including nociceptive pain, inflammatory pain, and neuropathic pain. studies have shown that TRP channels have a bi-directional effect on the regulation of crucial pain processes: transduction, transmission, and modulation [Citation24]:

a) Transduction is the process that nerve endings detect tissue-damaging injury: TRPs are nonselective cation channels with relatively high Ca2+ permeability, expressed in peripheral and central nervous system (CNS) terminals, and detect/transduce painful signals. For example, TRPV1 can be activated by capsaicin, acid, and heat [Citation25].

b) transmission is the process that relay signal messages from the site of tissue injury to the central nervous system: Though the dorsal root ganglion (DRG) and trigeminal ganglion (TG), afferent inputs from nociceptors enter the CNS for transmission to the cerebral cortex for interpretation [Citation26]. TRPV1 channels are expressed in DRG and TG and affect transmission in nociceptive neurons. TRPA1 is expressed in the dorsal horn of the spinal cord and promotes the release process of glutamate [Citation25]. TRPM2 and TRPM8 channels are also expressed in DRG and TG [Citation27].

c) Modulation is the neural process that reduces the transmission system and pain perception: It is worth noting that activating some TRP channels, such as TRPV1, TRPA1, and TRPM8, can modulate pain perception [Citation25,Citation28]. TRPM2-mediated infiltration of macrophages and microglia contribute to the pathogenesis of neuropathic pain, and TRPA1-mediated loss of substance P reduces tactile sensitivity in diabetic neuropathy [Citation29,Citation30]. AS TRP channels play a more and more important role in pain, many TRP channels are considered as potential therapeutic targets for pain management [Citation31,Citation32].

③ TRP channels accelerates lung inflammation

TRP channels are expressed in the lung endothelium [Citation33–36]. AS a second messenger, they mediate Ca2+ influx and signaling to regulate endothelial permeability, vasodilation, angiogenesis, inflammation, and pathophysiological response [Citation37–40]. TRP heteromers – TRPC1/4, TRPC3/6, and TRPV1/4-play a crucial role in pulmonary inflammation. They may extend openings to accelerate Ca2+ influx in order to promote a CaM/MLCK-signaling-dependent increase in endothelial permeabilIty, and disrupt endothelial barrier function more profoundly [Citation41].

Keyword co-occurrence and burst

Keywords were identified and analyzed using strong citation bursts () to explore research hotspots, frontiers, and emerging trends over time. As shown in (), the red line indicates the period of time during which the burst keyword appears [Citation42]. The citation burst time of keywords including “molecular docking”(2017–2021, 43.06), “contribute”(2017–2021, 38.07), “cytokine”(2019–2021, 36.2), “autophagy”(2019–2021, 34.25), “risk”(2019–2021, 33.86), “performance”(2018–2021, 26.79), “antioxidant”(2017–2021, 26.3), and “design”(2018–2021,22.09) has continued to 2021, and are still ongoing, reveals that these directions have great potential.

Table 6. Top 25 keywords with the strongest citation bursts

Conclusions

Based on the WOSCC database, bibliometric and Visual analysis were used to study the characteristics of TRP channels research results from 2012 to 2021. The number of publications on TRP channels has maintained over 2,500 per year. There will be a dramatically increasing number of publications on TRP research based on the current global trends. The hot spots of TRP channels research were “pain,” “calcium,” “inflammation,” and “oxidative stress.” The top research frontiers were “molecular docking,” “cytokine,” and “autophagy.” Bibliometric analysis of the literature on the TRP channels contributes researchers to identify cooperations, find research hotspots, and predict the frontiers of chloride channel research.

Disclosure statement

The authors report no conflicts of interest in this work.

Additional information

Funding

This work was supported by the A studio established by recognized leaders in the field of public service.

References

  • Tsagareli MG, Nozadze I. An overview on transient receptor potential channels superfamily. Behav Pharmacol. 2020 Aug;31(5):413–434.
  • Chen C, Dubin R, Kim MC. Emerging trends and new developments in regenerative medicine: a scientometric update (2000-2014). Expert Opin Biol Ther. 2014 Sep;14(9):1295–1317.
  • Wang Q, Yang Z, Yang Y, et al. A bibliometric analysis of research on the risk of engineering nanomaterials during 1999-2012. Sci Total Environ. 2014 Mar 1;473-474:483–489.
  • Chen C, Song M, Glanzel W. Visualizing a field of research: a methodology of systematic scientometric reviews. PLoS One. 2019 Oct 31;14(10):e0223994.
  • Chen C. Searching for intellectual turning points: progressive knowledge domain visualization. Proc Natl Acad Sci U S A. 2004 Apr 6;101 Suppl 1(Suppl1):5303–5310.
  • Van Eck NJ, Waltman L. Software survey: vOSviewer, a computer program for bibliometric mapping. Scientometrics. 2010 Aug;84(2):523–538.
  • Qin Y, Zhang Q, Liu Y. Analysis of knowledge bases and research focuses of cerebral ischemia-reperfusion from the perspective of mapping knowledge domain. Brain Res Bull. 2020;156:15–24.
  • Briganti M, Delnevo CD, Brown L, et al. Bibliometric analysis of electronic cigarette publications: 2003⁻2018. Int J Environ Res Public Health. 2019 Jan 24;16(3):320.
  • Ghorbani F, Feizabadi M, Farzanegan R, et al. An investigation of topics and trends of tracheal replacement studies using co-occurrence analysis. Tissue Eng Part B Rev. 2017 Apr;23(2):118–127.
  • Liang YD, Li Y, Zhao J, et al. Study of acupuncture for low back pain in recent 20 years: a bibliometric analysis via CiteSpace. J Pain Res. 2017;10:951–964.
  • Tominaga M. The role of TRP channels in thermosensation. Liedtke WB, Heller S, editors. TRP ion channel function in sensory transduction and cellular signaling cascades. Boca Raton (FL):CRC Press/Taylor & Francis; 2007. Chapter 20, pp. 1-13.
  • Tominaga M, Caterina MJ. Thermosensation and pain. J Neurobiol. 2004 Oct;61(1):3–12.
  • Liao M, Cao E, Julius D, et al. Structure of the TRPV1 ion channel determined by electron cryo-microscopy. Nature. 2013 Dec 5;504(7478):107–112.
  • Cao E, Liao M, Cheng Y, et al. TRPV1 structures in distinct conformations reveal activation mechanisms. Nature. 2013 Dec 5;504(7478):113–118.
  • Paulsen CE, Armache JP, Gao Y, et al. Structure of the TRPA1 ion channel suggests regulatory mechanisms. Nature. 2015 Apr 23;520(7548):511–517.
  • Gao Y, Cao E, Julius D, et al. TRPV1 structures in nanodiscs reveal mechanisms of ligand and lipid action. Nature. 2016 Jun 16;534(7607):347–351.
  • Chen C. CiteSpace II: detecting and visualizing emerging trends and transient patterns in scientific literature. J Am Soc Inf Sci Technol. 2006;57(3):359–377.
  • Duitama M, Vargas-López V, Casas Z, et al. TRP channels role in pain associated with neurodegenerative diseases. Front Neurosci. 2020 Aug;4(14):782.
  • Lv H, Yue J, Chen Z, et al. Effect of transient receptor potential vanilloid-1 on cough hypersensitivity induced by particulate matter 2.5. Life Sci. 2016 Apr 15;151:157–166.
  • Sadofsky LR, Ramachandran R, Crow C, et al. Inflammatory stimuli up-regulate transient receptor potential vanilloid-1 expression in human bronchial fibroblasts. Exp Lung Res. 2012 Mar;38(2):75–81.
  • Phan TX, Ton HT, Gulyás H, et al. TRPV1 expressed throughout the arterial circulation regulates vasoconstriction and blood pressure. J Physiol. 2020 Dec;598(24):5639–5659.
  • Kossakowski R, Schlicker E, Toczek M, et al. Cannabidiol affects the bezold-jarisch reflex via TRPV1 and 5-HT3 receptors and has peripheral sympathomimetic effects in spontaneously hypertensive and normotensive rats. Front Pharmacol. 2019 May 22;10:500.
  • Dou M, Ma Z, Cheng X, et al. Intrathecal lentivirus-mediated RNA interference targeting nerve growth factor attenuates myocardial ischaemia-reperfusion injury in rat. Br J Anaesth. 2019 Oct;123(4):439–449.
  • Mickle AD, Shepherd AJ, Mohapatra DP. Sensory TRP channels: the key transducers of nociception and pain. Prog Mol Biol Transl Sci. 2015;131:73–118.
  • Koivisto A, Chapman H, Jalava N, et al. TRPA1: A transducer and amplifier of pain and inflammation. Basic Clin Pharmacol Toxicol. 2014 Jan;114(1):50–55.
  • Yam MF, Loh YC, Tan CS, et al. General pathways of pain sensation and the major neurotransmitters involved in pain regulation. Int J Mol Sci. 2018 Jul 24;19(8):2164.
  • González-Ramírez R, Chen Y, Liedtke WB, et al. TRP channels and pain. In: Emir TLR, eds. Neurobiology of TRP channels. Boca Raton (FL): CRC Press/Taylor & Francis; 2017. Chapter 8, pp.1-24.
  • Takayama Y, Derouiche S, Maruyama K, et al. Emerging perspectives on pain management by modulation of TRP channels and ANO1. Int J Mol Sci. 2019 Jul 11;20(14):3411.
  • Basso L, Altier C. Transient receptor potential channels in neuropathic pain. Curr Opin Pharmacol. 2017 Feb;32:9–15.
  • Isami K, Haraguchi K, So K, et al. Involvement of TRPM2 in peripheral nerve injury-induced infiltration of peripheral immune cells into the spinal cord in mouse neuropathic pain model. PLoS One. 2013 Jul 30;8(7):e66410.
  • Moran MM. TRP channels as potential drug targets. Annu Rev Pharmacol Toxicol. 2018 Jan;6(58):309–330.
  • Huang Y, Fliegert R, Guse AH, et al. A structural overview of the ion channels of the TRPM family. Cell Calcium. 2020 Jan;85:102111.
  • Paria BC, Vogel SM, Ahmmed GU, et al. Tumor necrosis factor-alpha-induced TRPC1 expression amplifies store-operated Ca2+ influx and endothelial permeability. Am J Physiol Lung Cell Mol Physiol. 2004 Dec;287(6):L1303–13.
  • Ma X, Cheng KT, Wong CO, et al. Heteromeric TRPV4-C1 channels contribute to store-operated Ca(2+) entry in vascular endothelial cells. Cell Calcium. 2011 Dec;50(6):502–509.
  • Yin J, Michalick L, Tang C, et al. Role of transient receptor potential vanilloid 4 in neutrophil activation and acute lung injury. Am J Respir Cell Mol Biol. 2016 Mar;54(3):370–383.
  • Hecquet CM, Zhang M, Mittal M, et al. Cooperative interaction of trp melastatin channel transient receptor potential (TRPM2) with its splice variant TRPM2 short variant is essential for endothelial cell apoptosis. Circ Res. 2014 Jan 31;114(3):469–479.
  • Simmons S, Erfinanda L, Bartz C, et al. Novel mechanisms regulating endothelial barrier function in the pulmonary microcirculation. J Physiol. 2019 Feb;597(4):997–1021.
  • Earley S, Brayden JE. Transient receptor potential channels in the vasculature. Physiol Rev. 2015 Apr;95(2):645–690.
  • Moccia F, Guerra G. Ca(2+) signalling in endothelial progenitor cells: Friend or foe? J Cell Physiol. 2016 Feb;231(2):314–327.
  • Smani T, Gómez LJ, Regodon S, et al. TRP channels in angiogenesis and other endothelial functions. Front Physiol. 2018 Dec;3(9):1731.
  • Zergane M, Kuebler WM, Michalick L. Heteromeric TRP channels in lung inflammation. Cells. 2021 Jul 1;10(7):1654.
  • Papke RL. Merging old and new perspectives on nicotinic acetylcholine receptors. Biochem Pharmacol. 2014 May 1;89(1):1–11.