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International Journal of Immunopathology and Pharmacology logoLink to International Journal of Immunopathology and Pharmacology
. 2021 May 13;35:20587384211015054. doi: 10.1177/20587384211015054

Therapeutic effects of SKF-96365 on murine allergic rhinitis induced by OVA

Guangyi Ba 1,2,3,*, Ru Tang 1,2,3,*, Xiwen Sun 1,2,3, Zhipeng Li 1,2,3, Hai Lin 1,2,3,✉, Weitian Zhang 1,2,3
PMCID: PMC8127738  PMID: 33983057

Abstract

Introduction:

SKF-96365 is regarded as an inhibitor of receptor-mediated calcium ion (Ca2+) entry. The current study aimed to explore the effects of SKF-96365 on murine allergic rhinitis (AR).

Methods:

Intranasal SKF-96365 administration was performed on OVA induced murine AR. Serum and nasal lavage fluid (NLF) from mice were harvested to assay IgE and inflammatory cytokines using ELISA method. Inflammatory cells were counted and analyzed in NLF. Nasal mucosa tissues were collected from mice and used for HE staining, immunohistochemistry (IHC) staining, and real-time PCR detection.

Results:

SKF-96365 had therapeutic effects on murine AR manifesting attenuation of sneezing, nasal rubbing, IgE, inflammatory cytokines, inflammatory cells, TRPC6 immunolabeling, and TRPC6, STIM1 and Orai1 mRNA levels in AR mice.

Conclusion:

SKF-96365 could effectively alleviate the symptoms of murine AR. SKF-96365 could suppress TRPC6, STIM1, and Orai1 activities, leading to the downregulation of inflammatory cytokines and inflammatory cells in murine AR.

Keywords: allergic rhinitis, SKF-96365, calcium, TRPC6, STIM1, Orai1, ovalbumin

Introduction

Allergic rhinitis (AR) is a common allergen-induced and IgE-mediated disorder of the nasal mucosa characterized by rhinorrhea, sneezing, itching, and nasal congestion.1,2 AR has adverse effects on the patients’ quality of life and work,3 and the pathogenesis of AR is still uncertain.4

Glucocorticosteroids and antihistamines are effective in the therapy of AR, however, they only have temporary reliefs and some AR patients are insensitive or tolerant to them.5 Therefore, a novel drug with better effects is in great demand.

Considerable data indicate that calcium ion (Ca2+) is an essential second messenger inducing a signaling cascade in many immune responses, and Ca2+ influx is mediated by Ca2+ channels distributed in various cells.6 Transient receptor potential canonical channel 6 (TRPC6) and store-operated calcium entry (SOCE) mediated by stromal interaction molecule1 (STIM1) and Orai1 play pivotal roles in mediating Ca2+ influx in a variety of cells.7–9 Our previous work showed that TRPC6 can synergize with STIM1 and Orai1 to modulate Ca2+ influx of nasal epithelial cells (NECs) and then trigger inflammatory response in chronic rhinosinusitis with nasal polyp.10

1-[2-(4-methoxyphenyl)-2-[3-(4-methoxyphenyl) propoxy]ethyl-1H-imidazole (SKF-96365) is a small molecule compound acting as a non-selective inhibitor of TRP channels, SOCE and voltage-gated Ca2+ channels, and SKF-96365 has been proved to suppress cellular Ca2+ influx via inhibiting these Ca2+ channels.11–13 There is ample evidence that SKF-96365 is widely used to study the function of TRPC channels.12–17 Previous reports indicate that SKF 96365 could suppress cardiomyocyte hypertrophy, and inhibit spontaneous nociception and pain hypersensitivity induced by melittin via inactivating TRPC channels and Ca2+ influx.12,18 In cultured NECs, TRPC6, STIM1, Orai1, Ca2+ MFI levels, and inflammatory mediators were upregulated by lipopolysaccharide (LPS) and 1-oleoyl-2-acetyl-glycerol (OAG, diacylglycerol (DAG) analog, TRPC6 activator), but were inhibited by SKF-96365.10 In addition, 2-aminoethoxydiphenyl borate (2-APB) is a chemical which could inhibit SOCE and TRP channels,19,20 and one previous report has indicated that 2-APB administration intranasally could reduce numbers of sneezing, nasal rubbing, and eosinophils in murine AR.21 However, little is known about the effects of SKF-96365 on murine AR. Therefore, we conducted this study to explore the therapeutic effects of SKF-96365 on murine AR.

Materials and methods

Animals

Female BALB/c mice were purchased and maintained under a pathogen-free condition. To exclude off-target effects and prove the specificity of the findings, we included a second inhibitor 2-APB, TRPC6 activator OAG, and dexamethasone (Dex) as controls. We classified the mice into seven groups (n = 10 each group): normal control group, 100 μg Dex treated AR group, 200 μg 2-APB treated AR group, 400 μg SKF-96365 treated AR group, 200 μg SKF-96365 treated AR group, untreated AR group, and 100 μg OAG treated AR group. Detailed information of murine AR model establishment and treatment was listed in Table 1. This study was approved by the Animal Ethics Committee of Shanghai Sixth People’s Hospital.

Table 1.

Detailed information of murine AR model establishment and treatment.

Group N IP sensitization stage (days 1, 8, and 15) IN challenge stage (days 22–29) Drugs dose
Control 10 Normal saline Normal saline
OVA + Dex 10 OVA/Alum sensitization OVA + Dex 100 μg
OVA + 2-APB 10 OVA/Alum sensitization OVA + 2-APB 200 μg
OVA + SKF-400 μg 10 OVA/Alum sensitization OVA + SKF-96365 400 μg
OVA + SKF-200 μg 10 OVA/Alum sensitization OVA + SKF-96365 200 μg
OVA 10 OVA/Alum sensitization OVA
OVA + OAG 10 OVA/Alum sensitization OVA + OAG 100 μg
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AR: allergic rhinitis; N: number; IP: intraperitoneal; IN: intranasal; OVA: ovalbumin; Dex: dexamethasone; Alum: aluminum hydroxide; 2-APB: 2-aminoethoxydiphenyl borate; SKF or SKF-96365: 1-[2-(4-methoxyphenyl)-2-[3-(4-methoxyphenyl) propoxy]ethyl-1H-imidazole; OAG: 1-oleoyl-2-acetyl-glycerol.

Murine AR model was established according to a previously used protocol.22 Briefly, mice were sensitized intraperitoneally with 100 μg ovalbumin (OVA) and aluminum hydroxide (4 mg) in 0.2 ml sterile saline on days 1, 8, and 15 (Figure 1). Then, on days 22–29, the mice were challenged intranasally with 40 mg/ml OVA diluted in 20 μl sterile saline. In addition, on days 22–29, SKF-96365 (200 or 400 μg, Abcam, Figure 1), 2-APB (200 μg, Abcam), OAG (100 μg, Abcam), or Dex (100 μg, Sigma-Aldrich) was administrated intranasally on AR mice 1 h before OVA challenge. The subjective measurements including sneezing, inflammatory cells, eosinophils, and TRPC6 immunolabeling were evaluated by the investigators blinded to the study. More detailed protocols were provided in the Supplemental Material.

Figure 1.

Figure 1.

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Schematic diagram demonstrating the process of AR mouse model construction and SKF-96365 treatment.

Evaluation of nasal symptoms and sample collection

Nasal symptoms were evaluated by counting the frequencies of sneezing and nasal rubbing during the 15-min period 10 min after final OVA challenge on day 29. Then, blood, NLF, and nasal mucosas were collected from mice to perform experiment research. More detailed protocols were provided in the Supplemental Material.

ELISA and inflammatory cells counting

OVA-specific IgE, histamines, and LTC4 concentrations (BlueGene Biotech, Shanghai, China) in serum samples and OVA-specific IgE, IL-4, IL-5, IL-6, IL-13, and IL-33 concentrations (BlueGene Biotech) in NLF samples were detected by ELISA. Additionally, total cells, eosinophils, macrophages, neutrophils, and lymphocytes in the NLF were counted after Wright-Giemsa staining. More detailed protocols were provided in the Supplemental Material.

HE and IHC staining

Eosinophils and TRPC6 immunoreactivity in nasal mucosas of mice were evaluated by HE and IHC staining. More detailed protocols were provided in the Supplemental Material.

Real-time reverse transcriptions PCR

Real-time PCR was used to detect TRPC6, STIM1, and Orai1 mRNA levels in nasal mucosas of mice. More detailed protocols were provided in the Supplemental Material.

Statistical analysis

Values were noted as mean ± standard error of mean (SEM). One-way ANOVA with Bonferroni post hoc test was employed for intergroup comparison. Two-sided P value <0.05 was deemed statistically significant.

Results

Effects of SKF-96365 on frequencies of sneezing and nasal rubbing in AR mice

Of note, untreated AR mice exhibited significantly elevated frequencies of sneezing and nasal rubbing compared with normal control mice, and SKF-96365 treated AR mice (200 or 400 μg), 2-APB and Dex treated AR mice manifested significantly decreased frequencies of sneezing, and nasal rubbing compared to untreated AR mice (Figure 2a and b). Nonetheless, OAG treated AR mice manifested obviously elevated frequencies of sneezing and nasal rubbing compared to untreated AR mice (Figure 2a and b). In addition, SKF-96365 (400 μg) was more effective in comparison to SKF-96365 (200 μg) (Figure 2a and b).

Figure 2.

Figure 2.

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(a)–(k) Sneezing, nasal rubbing and OVA-specific IgE, histamines and LTC4 levels in the serum, and OVA-specific IgE, IL-4, IL-5, IL-6, IL-13, and IL-33 levels in the NLF from normal control group, 100 μg Dex treated AR group (OVA + Dex), 200 μg 2-APB treated AR group (OVA + 2-APB), 400 μg SKF-96365 treated AR group (OVA + 400 μg SKF), 200 μg SKF-96365 treated AR group (OVA + 200 μg SKF), untreated AR group (OVA), and 100 μg OAG treated AR group (OVA + OAG).

ELISA assay in the serum and NLF and inflammatory cells in the NLF

Notably, untreated AR mice manifested significant elevation of OVA-specific IgE, histamines, and LTC4 levels in serum, and OVA-specific IgE, IL-4, IL-5, IL-6, IL-13, and IL-33 levels in NLF compared to normal control mice, and these measurements were obviously decreased in SKF-96365 treated AR mice (200 or 400 μg), 2-APB and Dex treated AR mice in comparison to untreated AR mice (Figure 2c–k). Nonetheless, these measurements were obviously increased in OAG treated AR mice in comparison to untreated AR mice (Figure 2c–k). Furthermore, these effects were more obvious in SKF-96365 (400 μg) treated AR mice in comparison to SKF-96365 treated (200 μg) AR mice (Figure 2c–k).

Effects of SKF-96365 on inflammatory cells in the NLF

Furthermore, untreated AR mice manifested significant elevation of total cells, eosinophils, macrophages, neutrophils, and lymphocytes numbers in NLF compared to normal control mice (Figure 3a–e). Additionally, these cells were diminished in SKF-96365 treated AR mice (200 or 400 μg), 2-APB and Dex treated AR mice compared to untreated AR mice (Figure 3a–e). Nonetheless, these cells numbers were obviously increased in OAG treated AR mice in comparison to untreated AR mice (Figure 3a–e). Furthermore, these effects were more obvious in SKF-96365 (400 μg) treated AR mice in comparison to SKF-96365 treated (200 μg) AR mice (Figure 3a–e).

Figure 3.

Figure 3.

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(a)–(e) Total cells, eosinophils, macrophages, neutrophils, and lymphocytes in the NLF from normal control group, 100 μg Dex treated AR group (OVA + Dex), 200 μg 2-APB treated AR group (OVA + 2-APB), 400 μg SKF-96365 treated AR group (OVA + 400 μg SKF), 200 μg SKF-96365 treated AR group (OVA + 200 μg SKF), untreated AR group (OVA), and 100 μg OAG treated AR group (OVA + OAG).

Effects of SKF-96365 on eosinophils in nasal mucosas

Of interest, untreated AR mice manifested significant elevation of eosinophils numbers in nasal mucosas compared to normal control mice, and SKF-96365 treated AR mice (200 or 400 μg), 2-APB and Dex treated AR mice exhibited marked decline of eosinophils numbers compared to untreated AR mice (Figure 4a–h). Nonetheless, eosinophils numbers were obviously increased in OAG treated AR mice in comparison to untreated AR mice (Figure 4a–h). Furthermore, these effects were more obvious in SKF-96365 (400 μg) treated AR mice in comparison to SKF-96365 treated (200 μg) AR mice (Figure 4a–h).

Figure 4.

Figure 4.

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(a)–(h) HE staining for eosinophils in nasal tissues from normal control group, 100 μg Dex treated AR group (OVA + Dex), 200 μg 2-APB treated AR group (OVA + 2-APB), 400 μg SKF-96365 treated AR group (OVA + 400 μg SKF), 200 μg SKF-96365 treated AR group (OVA + 200 μg SKF), untreated AR group (OVA), and 100 μg OAG treated AR group (OVA + OAG).

Red arrows indicate eosinophils having two-lobed nuclei connected by a band of nuclear material. Scale bar = 20 μm.

Effects of SKF-96365 on TRPC6 immunolabeling in nasal mucosas

TRPC6 positive cells were mainly epithelial cells and sub-mucosal inflammatory cells in the nasal mucosa (Figure 5a–g). Of note, untreated AR mice manifested significant elevation of TRPC6 immunolabeling compared to normal control mice, and TRPC6 immunolabeling was significantly downregulated in SKF-96365 treated AR mice (200 or 400 μg), 2-APB and Dex treated AR mice compared to untreated AR mice (Figure 5a–i). Nonetheless, TRPC6 immunolabeling was obviously increased in OAG treated AR mice in comparison to untreated AR mice (Figure 5a–i). In addition, these effects were more obvious in SKF-96365 (400 μg) treated AR mice in comparison to SKF-96365 treated (200 μg) AR mice (Figure 5a–i).

Figure 5.

Figure 5.

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(a)–(l) TRPC6 immunolabeling, and mRNA levels of TRPC6, STIM1 Orai1 in nasal tissues from normal control group, 100 μg Dex treated AR group (OVA + Dex), 200 μg 2-APB treated AR group (OVA + 2-APB), 400 μg SKF-96365 treated AR group (OVA + 400 μg SKF), 200 μg SKF-96365 treated AR group (OVA + 200 μg SKF), untreated AR group (OVA), and 100 μg OAG treated AR group (OVA + OAG).

Scale bar = 20 μm.

Effects of SKF-96365 on TRPC6, STIM1 and Orai1 mRNA levels in nasal mucosas

Of note, untreated AR mice manifested significant elevation of TRPC6, STIM1, and Orai1 mRNA levels compared to normal control mice, and these measurements were obviously decreased in SKF-96365 treated AR mice (200 or 400 μg), 2-APB and Dex treated AR mice compared to untreated AR mice (Figure 5j–l). Nonetheless, these measurements were obviously elevated in OAG treated AR mice in comparison to untreated AR mice (Figure 5j–l). Furthermore, these effects were more obvious in SKF-96365 (400 μg) treated AR mice in comparison to SKF-96365 treated (200 μg) AR mice (Figure 5j–l).

Discussion

It is generally acknowledged that Ca2+ signaling and related Ca2+ channels are essential to elicit allergic and inflammatory responses.23–25 Our previous studies demonstrated that KCa3.1, STIM1, and Orai1 play pivotal roles in mediating Ca2+ signaling in the pathogenesis of AR.26 TRPC6, one type of Ca2+ channels, has been proved to play key roles in mediating intracellular Ca2+ homeostasis in the processes of cell growth, cell migration, and cell activation.8 It has been revealed that TRPC6 and Ca2+ influx in bronchial epithelial cells could be increased by LPS and then inflammatory response was triggered.27 In addition, TRPC6 is involved in the etiology and pathophysiology of asthma, COPD, lung fibrosis, and lung edema.28,29 Our previous work showed that TRPC6 modulates cellular Ca2+ influx via collaborating with STIM1 and Orai1 in nasal epithelial cells, and these effects could be enhanced by OAG and suppressed by SKF-96365.10

Considerable data indicate that SKF-96365 is a calcium antagonist which plays key roles in the inhibition of cellular Ca2+ influx via inactivating TRPC channels and SOCE in a variety of cells, and has been widely used to explore the pathophysiological function of TRPC channels and SOCE in non-excitable cells and excitable cells.30,31 Accumulating evidence indicates that SKF-96365 could suppress hypoxic pulmonary vasoconstriction,17 inhibit in vitro cultured mouse airway smooth muscle cells proliferation induced by ESI-09,32 and regulate apoptosis and autophagy in colorectal cancer cells.31 However, there is a lack of data regarding the effects of SKF-96365 on murine AR. Thus, we performed this study to explore the therapeutic effects of SKF-96365 on murine AR. To exclude off-target effects and prove the specificity of the findings, we included a second inhibitor 2-APB, TRPCs activator OAG, and Dex as controls. As described previously33,34, 2-APB could exert its role at the concentration of 5–50 μM. As the molecular weight of 2-APB is 225.09, doses range = (5–50 μM) × 0.030 l = (5 × 225.09–50 × 225.09 μg/l) × 0.030 l = 33.7635 μg–337.635 μg, the 200 μg dose of 2-APB used in our study was among the range (approximately 29.6178 μM which is close to the dose of 2-APB (30 μM) used to treat murine AR in the previous report21), and we also found 2-APB was effective in the treatment of murine AR and the findings are partially in line with this previous report.21

The in vivo findings indicated that untreated AR mice manifested significant elevation of sneezing, nasal rubbing, OVA-specific IgE, histamines and LTC4 levels in serum, OVA-specific IgE, IL-4, IL-5, IL-6, IL-13, IL-33 and inflammatory cells levels in NLF, eosinophils, TRPC6 immunolabeling, and TRPC6, STIM1 and Orai1 mRNA levels compared to normal control mice, and these effects were markedly decreased in SKF-96365 treated AR mice (200 or 400 μg), 2-APB and Dex treated AR mice compared to untreated AR mice. Nonetheless, these effects were markedly enhanced in OAG treated AR mice compared to untreated AR mice. Moreover, these effects were more obvious in SKF-96365 (400 μg) treated AR mice in comparison to SKF-96365 treated (200 μg) AR mice. The results demonstrate that SKF-96365 might suppress TRPC6, STIM1, and Orai1expression in nasal mucosas in AR mice, leading to the inhibition of allergic and inflammatory reactions manifesting decreased inflammatory cells numbers and inflammatory cytokines levels. These findings are partially in line with previous studies suggesting that administration of SKF-96365 could diminish TRPC6 protein expression in the hyperalgesia in diabetic rats,35 and modulate inflammatory reactions elicited by LPS and IFN-γ treatment in murine peritoneal macrophages.36 Of interest, our results are also in agreement with previous reports demonstrating that SKF-96365 could suppress human non-small cell lung cancer cell proliferation by blocking TRPC6,37 and reduce airway smooth muscle cells (ASMCs) proliferation via inhibiting STIM1/Orai1-mediated SOCE to decrease Ca2+ influx in ASMCs.38

Some limitations of our study should be noted. First, due to the cell diversity of nasal tissues, specific cells including eosinophils, mast cells, lymphocytes, dendritic cells or macrophages need to be isolated to further precisely assess the effects, and mechanism of SKF-96365 on the allergic response of AR. Second, due to the lack of specific inhibitors of TRPC6 and SOCE, we used the non-specific inhibitor SKF-96365 to treat murine AR, other possible off-target effects need to be further explored deeply in the future.

Conclusion

In summary, SKF-96365 could effectively alleviate the symptoms of murine AR. SKF-96365 could suppress TRPC6, STIM1, and Orai1 activities, leading to the downregulation of inflammatory cytokines and inflammatory cells in murine AR.

Supplemental Material

sj-doc-1-iji-10.1177_20587384211015054 – Supplemental material for Therapeutic effects of SKF-96365 on murine allergic rhinitis induced by OVA
Click here for additional data file. (70.5KB, doc)

Supplemental material, sj-doc-1-iji-10.1177_20587384211015054 for Therapeutic effects of SKF-96365 on murine allergic rhinitis induced by OVA by Guangyi Ba, Ru Tang, Xiwen Sun, Zhipeng Li, Hai Lin and Weitian Zhang in International Journal of Immunopathology and Pharmacology

Footnotes

Declaration of conflicting interests: The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Funding: The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This work was supported by the National Natural Science Foundation of China (No. 81870700, No. 82071014, and No. 82000951), Shanghai Natural Science Foundation of China (No. 16ZR1426100), Science and Technology Innovation Action Plan of Science and Technology Commission of Shanghai Municipality (No. 19411950700), the Key Laboratory Funding of Science and Technology Commission of Shanghai Municipality (No. 18DZ2260200), and Shanghai Shen-Kang Hospital Management Center Project (SHDC12020129).

Ethical approval: Ethical approval for this study was obtained the Animal Ethics Committee of Shanghai Sixth People’s Hospital (No. 2020-0201).

Animal welfare: The present study followed international, national, and/or institutional guidelines for humane animal treatment and complied with relevant legislation of the country.

Supplementary material: Supplemental material for this article is available online.

References

  • 1. Demoly P, Corren J, Creticos P, et al. (2021) A 300 IR sublingual tablet is an effective, safe treatment for house dust mite-induced allergic rhinitis: An international, double-blind, placebo-controlled, randomized phase III clinical trial. The Journal of Allergy and Clinical Immunology 147(3): 1020–1030.e10. [DOI] [PubMed] [Google Scholar]
  • 2. Liu H, Wang T, Xia J, et al. (2020) Cholinergic neuron-like D-U87 cells promote polarization of allergic rhinitis T-helper 2 cells. International Forum of Allergy & Rhinology 10: 233–242. [DOI] [PubMed] [Google Scholar]
  • 3. Huang R, Mao W, Wang G, et al. (2020) Synergistic relationship between TSLP and IL-33/ST2 signaling pathways in allergic rhinitis and the effects of hypoxia. International Forum of Allergy & Rhinology 10: 511–520. [DOI] [PubMed] [Google Scholar]
  • 4. Gultuna S, Tezel N, Ozalp Ates FS. (2019) Fibromyalgia in the patients with allergic rhinitis: Its prevalence and impact on the quality of life. The American Journal of Rhinology & Allergy 33(6):716–722. [DOI] [PubMed] [Google Scholar]
  • 5. Watts AM, Cripps AW, West NP, et al. (2019) Modulation of allergic inflammation in the nasal mucosa of allergic rhinitis sufferers with topical pharmaceutical agents. Frontiers in Pharmacology 10: 294. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6. Zophel D, Hof C, Lis A. (2020) Altered Ca(2+) homeostasis in immune cells during aging: Role of ion channels. International Journal of Molecular Sciences 22(1): 110. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7. Jardin I, Nieto J, Salido GM, et al. (2020) TRPC6 channel and its implications in breast cancer: An overview. Biochimica et Biophysica Acta (BBA)-Molecular Cell Research 1867: 118828. [DOI] [PubMed] [Google Scholar]
  • 8. Liu L, Gu L, Chen M, et al. (2020) Novel targets for stroke therapy: Special focus on TRPC channels and TRPC6. Frontiers in Aging Neuroscience 12: 70. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9. Chaudhari S, Mallet RT, Shotorbani PY, et al. (2021) Store-operated calcium entry: Pivotal roles in renal physiology and pathophysiology. Experimental Biology and Medicine (Maywood) 246: 305–316. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10. Tang R, Li ZP, Li MX, et al. (2018) Pro-inflammatory role of transient receptor potential canonical channel 6 in the pathogenesis of chronic rhinosinusitis with nasal polyps. International Forum of Allergy & Rhinology 8: 1334–1341. [DOI] [PubMed] [Google Scholar]
  • 11. Wen H, Gwathmey JK, Xie LH. (2020) Role of transient receptor potential canonical channels in heart physiology and pathophysiology. Frontiers in Cardiovascular Medicine 7: 24. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12. Cheng H, Li J, Wu Q, et al. (2020) Effect of SKF96365 on cardiomyocyte hypertrophy induced by angiotensin II. Molecular Medicine Reports 21: 806–814. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13. Krolik A, Diamandakis D, Zych A, et al. (2020) The involvement of TRP channels in memory formation and task retrieval in a passive avoidance task in one-day old chicks. Neurobiology of Learning and Memory 171: 107209. [DOI] [PubMed] [Google Scholar]
  • 14. Lopez JR, Uryash A, Faury G, et al. (2020) Contribution of TRPC channels to intracellular Ca(2+) dyshomeostasis in smooth muscle from mdx mice. Frontiers in Physiology 11: 126. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15. Liu Z, Du Z, Li K, et al. (2020) TRPC6-mediated Ca(2+) entry essential for the regulation of Nano-ZnO induced autophagy in SH-SY5Y cells. Neurochemical Research 45: 1602–1613. [DOI] [PubMed] [Google Scholar]
  • 16. Hu Q, Ahmad AA, Seidel T, et al. (2020) Location and function of transient receptor potential canonical channel 1 in ventricular myocytes. Journal of Molecular and Cellular Cardiology 139: 113–123. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17. Jain PP, Hosokawa S, Xiong M, et al. (2020) Revisiting the mechanism of hypoxic pulmonary vasoconstriction using isolated perfused/ventilated mouse lung. Pulmonary Circulation 10: 2045894020956592. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18. Ding J, Zhang JR, Wang Y, et al. (2012) Effects of a non-selective TRPC channel blocker, SKF-96365, on melittin-induced spontaneous persistent nociception and inflammatory pain hypersensitivity. Neuroscience Bulletin 28: 173–181. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19. Makarenko VV, Peng YJ, Khan SA, et al. (2019) Long-term facilitation of catecholamine secretion from adrenal chromaffin cells of neonatal rats by chronic intermittent hypoxia. Journal of Neurophysiology 122: 1874–1883. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20. Adhya P, Sharma SS. (2019) Redox TRPs in diabetes and diabetic complications: Mechanisms and pharmacological modulation. Pharmacological Research 146: 104271. [DOI] [PubMed] [Google Scholar]
  • 21. Lin L, Zheng C, Zhang L, et al. (2011) 2-Aminoethoxydiphenyl borate administration into the nostril alleviates murine allergic rhinitis. American Journal of Otolaryngology 32: 318–328. [DOI] [PubMed] [Google Scholar]
  • 22. Zhang W, Tang R, Ba G, et al. (2020) Anti-allergic and anti-inflammatory effects of resveratrol via inhibiting TXNIP-oxidative stress pathway in a mouse model of allergic rhinitis. The World Allergy Organization Journal 13: 100473. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23. Vangeel L, Voets T. (2019) Transient receptor potential channels and calcium signaling. Cold Spring Harbor Perspectives in Biology 11: a035048. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24. Nam JH, Kim WK. (2020) The role of TRP channels in allergic inflammation and its clinical relevance. Current Medicinal Chemistry 27: 1446–1468. [DOI] [PubMed] [Google Scholar]
  • 25. Kappel S, Borgstrom A, Stoklosa P, et al. (2019) Store-operated calcium entry in disease: Beyond STIM/Orai expression levels. Seminars in Cell & Developmental Biology 94: 66–73. [DOI] [PubMed] [Google Scholar]
  • 26. Lin H, Zheng C, Li J, et al. (2014) Ca2+ -activated K+ channel-3.1 blocker TRAM-34 alleviates murine allergic rhinitis. International Immunopharmacology 23: 642–648. [DOI] [PubMed] [Google Scholar]
  • 27. Zhou LF, Chen QZ, Yang CT, et al. (2018) TRPC6 contributes to LPS-induced inflammation through ERK1/2 and p38 pathways in bronchial epithelial cells. American Journal of Physiology-Cell Physiology 314: C278–C288. [DOI] [PubMed] [Google Scholar]
  • 28. Dietrich A. (2019) Modulators of transient receptor potential (TRP) channels as therapeutic options in lung disease. Pharmaceuticals (Basel) 12: 23. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29. Dietrich A, Steinritz D, Gudermann T. (2017) Transient receptor potential (TRP) channels as molecular targets in lung toxicology and associated diseases. Cell Calcium 67: 123–137. [DOI] [PubMed] [Google Scholar]
  • 30. Gruszczynska-Biegala J, Strucinska K, Maciag F, et al. (2020) STIM protein-NMDA2 receptor interaction decreases NMDA-dependent calcium levels in cortical neurons. Cells 9: 160. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31. Jing Z, Sui X, Yao J, et al. (2016) SKF-96365 activates cytoprotective autophagy to delay apoptosis in colorectal cancer cells through inhibition of the calcium/CaMKIIgamma/AKT-mediated pathway. Cancer Letters 372: 226–238. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32. Chen YF, Huang G, Wang YM, et al. (2019) Exchange protein directly activated by cAMP (Epac) protects against airway inflammation and airway remodeling in asthmatic mice. Respiratory Research 20: 285. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33. Schild A, Bhardwaj R, Wenger N, et al. (2020) Synthesis and pharmacological characterization of 2-Aminoethyl Diphenylborinate (2-APB) derivatives for inhibition of store-operated calcium entry (SOCE) in MDA-MB-231 breast cancer cells. International Journal of Molecular Sciences 21: 5604. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34. Zhang X, Xin P, Yoast RE, et al. (2020) Distinct pharmacological profiles of ORAI1, ORAI2, and ORAI3 channels. Cell Calcium 91: 102281. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35. Roa-Coria JE, Pineda-Farias JB, Barragan-Iglesias P, et al. (2019) Possible involvement of peripheral TRP channels in the hydrogen sulfide-induced hyperalgesia in diabetic rats. BMC Neuroscience 20: 1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36. Ye Y, Huang X, Zhang Y, et al. (2012) Calcium influx blocked by SK&F 96365 modulates the LPS plus IFN-gamma-induced inflammatory response in murine peritoneal macrophages. International Immunopharmacology 12: 384–393. [DOI] [PubMed] [Google Scholar]
  • 37. Yang LL, Liu BC, Lu XY, et al. (2017) Inhibition of TRPC6 reduces non-small cell lung cancer cell proliferation and invasion. Oncotarget 8: 5123–5134. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38. Zou JJ, Gao YD, Geng S, et al. (2011) Role of STIM1/Orai1-mediated store-operated Ca(2)(+) entry in airway smooth muscle cell proliferation. Journal of Applied Physiology (1985) 110: 1256–1263. [DOI] [PubMed] [Google Scholar]

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Supplementary Materials

sj-doc-1-iji-10.1177_20587384211015054 – Supplemental material for Therapeutic effects of SKF-96365 on murine allergic rhinitis induced by OVA
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Supplemental material, sj-doc-1-iji-10.1177_20587384211015054 for Therapeutic effects of SKF-96365 on murine allergic rhinitis induced by OVA by Guangyi Ba, Ru Tang, Xiwen Sun, Zhipeng Li, Hai Lin and Weitian Zhang in International Journal of Immunopathology and Pharmacology

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