Role of acetylcholine and acetylcholinesterase in improving abiotic stress resistance/tolerance

References

• Raza A, Salehi H, Rahman MA, et al. Plant hormones and neurotransmitter interactions mediate antioxidant defenses under induced oxidative stress in plants. Front Plant Sci. 2022;13. doi: 10.3389/fpls.2022.961872
   Web of Science ®Google Scholar
• Tanveer M, Shabala S. Neurotransmitters in signalling and adaptation to salinity stress in plants. In: Baluška F, Mukherjee S, Ramakrishna A, editors. Neurotransmitters in Plant Signaling and Communication. Springer Cham: Springer Nature; 2020 p. 49–15. doi:10.1007/978-3-030-54478-2
   Google Scholar
• Roshchina VAV. Neurotransmitters in plant life. CRC Press Boca Raton: Taylor & Francis group; 2001. p. 292. doi:10.1201/9781482279856
   Google Scholar
• Raza A, Salehi H, Rahman MA, et al. Plant hormones and neurotransmitter interactions mediate antioxidant defenses under induced oxidative stress in plants. Front Plant Sci. 2022;13:961872. doi: 10.3389/fpls.2022.961872
   PubMed Web of Science ®Google Scholar
• Barlow PW. Reflections on ‘plant neurobiology’. Biosystems. 2008;92(2):132–147. doi: 10.1016/j.biosystems.2008.01.004
   PubMed Web of Science ®Google Scholar
• Baluška F, Volkmann D, Menzel D. Plant synapses: actin-based domains for cell-to-cell communication. Trends Plant Sci. 2005;10(3):106–111. doi: 10.1016/j.tplants.2005.01.002
   Google Scholar
• Akula R, Mukherjee S. New insights on neurotransmitters signaling mechanisms in plants. Plant Signal Behav. 2020;15(6):1737450. doi: 10.1080/15592324.2020.1737450
   PubMed Web of Science ®Google Scholar
• Braga I, Pissolato MD, Souza GM. Mitigating effects of acetylcholine supply on soybean seed germination under osmotic stress. Braz J Bot. 2017;40(3):617–624. doi: 10.1007/s40415-017-0367-2
   Web of Science ®Google Scholar
• Momonoki YS, Oguri S, Whallon JH. Acetylcholine as a signaling system to environmental stimuli in plants: II. Ca2+ movement in the coleoptile node cells of heat-stressed Zea mays seedlings. Jpn J Crop Sci. 1997;66(4):682–690.
   Google Scholar
• Qin C, Su YY, Li BS, et al. Acetylcholine mechanism of action to enhance tolerance to salt stress in Nicotiana benthamiana. Photosynthetica. 2019;57(2):590–598. doi: 10.32615/ps.2019.084
   Web of Science ®Google Scholar
• Shen J, Qin C, Qin Y, et al. Acetylcholine alleviates salt stress in Zea mays L. by promoting seed germination and regulating phytohormone level and antioxidant capacity. J Plant Growth Regul. 2024;43(1):341–352. doi: 10.1007/s00344-023-11089-7
   Web of Science ®Google Scholar
• Brenner ED, Stahlberg R, Mancuso S, et al. Plant neurobiology: an integrated view of plant signaling. Trends Plant Sci. 2006;11(8):413–419. doi: 10.1016/j.tplants.2006.06.009
   PubMed Web of Science ®Google Scholar
• Wang H, Zhang S, Wang X, et al. Role of acetylcholine on plant root-shoot signal transduction. Chinese Sci Bull. 2003;48(6):570–573. doi: 10.1360/03tb9121
   Google Scholar
• Bamel K, Gupta SC, Gupta R. Acetylcholine causes rooting in leaf explants of in vitro raised tomato (Lycopersicon esculentum Miller) seedlings. Life Sci. 2007;80(24–25):2393–2396. doi: 10.1016/j.lfs.2007.01.039
   Web of Science ®Google Scholar
• Murata J, Watanabe T, Sugahara K, et al. High-resolution mass spectrometry for detecting Acetylcholine in Arabidopsis. Plant Signal Behav. 2015;10(10):e1074367. doi: 10.1080/15592324.2015.1074367
   Google Scholar
• Kostír J, Klenha J, Jirácek V. The effect of choline and acetylcholine on the seed germination of some economically important plants. I. 1965.
   Google Scholar
• Wang H, Wang X, Zhang S, et al. Muscarinic acetylcholine receptor is involved in acetylcholine regulating stomatal movement. Chin Sci Bull. 2000;45(3):250–252. doi: 10.1007/BF02884684
   Google Scholar
• Wang H, Zhang S, Wang X, et al. Involvement of Ca 2+/CaM in the signal transduction of acetylcholine regulating stomatal movement. Chin Sci Bull. 2003;48(4):351–354. doi: 10.1007/BF03183228
   Google Scholar
• Leng Q, Hua B, Guo Y, et al. Regulating role of acetylcholine and its antagonists in inward rectified K+ channels from guard cell protoplasts of Vicia faba. Sci China Ser Life Sci. 2000;43(2):217–224. doi: 10.1007/BF02879131
   Web of Science ®Google Scholar
• Volkov AG, Carrell H, Markin VS. Biologically closed electrical circuits in Venus flytrap. Plant Physiol. 2009;149(4):1661–1667. doi: 10.1104/pp.108.134536
   Web of Science ®Google Scholar
• Tezuka T, Akita I, Yoshino N. Self-incompatibility involved in the level of acetylcholine and cAMP. Plant Signal Behav. 2007;2(6):475–476. doi: 10.4161/psb.2.6.4483
   PubMedGoogle Scholar
• Tezuka T, Akita I, Yoshino N, et al. Regulation of self-incompatibility by acetylcholine and cAMP in Lilium longiflorum. J Plant Physiol. 2007;164(7):878–885. doi: 10.1016/j.jplph.2006.05.013
   Web of Science ®Google Scholar
• Sugiyama K-I, Tezuka T. Acetylcholine promotes the emergence and elongation of lateral roots of Raphanus sativus. Plant Signal Behav. 2011;6(10):1545–1553. doi: 10.4161/psb.6.10.16876
   PubMed Web of Science ®Google Scholar
• Wiśniewska J, Tretyn A. Acetylcholinesterase activity in Lycopersicon esculentum and its phytochrome mutants. Plant Physiol Biochem. 2003;41(8):711–717. doi: 10.1016/S0981-9428(03)00111-6
   Google Scholar
• Fluck RA, Leber PA, Lieser JD, et al. Choline conjugates of auxins. I. Direct evidence for the hydrolysis of choline-auxin conjugates by pea cholinesterase. Plant Physiol Biochem. 2000;38(4):301–308. doi: 10.1016/S0981-9428(00)00742-7
   Web of Science ®Google Scholar
• Dekhuijzen H. The effect of acetylcholine on growth and on growth inhibition by CCC in wheat seedlings. Planta. 1973;111(2):149–156. doi: 10.1007/BF00386275
   Google Scholar
• Evans ML. Promotion of cell elongation in Avena coleoptiles by acetylcholine. Plant Physiol. 1972;50(3):414. doi: 10.1104/pp.50.3.414
   Web of Science ®Google Scholar
• Jones RS, Stutte CA. Acetylcholine and red-light influence on ethylene evolution from soyabean leaf tissues. Ann Bot. 1986;57(6):897–900. doi: 10.1093/oxfordjournals.aob.a087175
   Web of Science ®Google Scholar
• Lawson VR, Brady RM, Campbell A, et al. Interaction of acetylcholine chloride with IAA, GA3 and red light in the growth of excised apical coleoptile segments. Bull Torrey Bot Club. 1978;105(3):187–191. doi: 10.2307/2484113
   Google Scholar
• Wessler I, Kilbinger H, Bittinger F, et al. The non-neuronal cholinergic system the biological role of non-neuronal acetylcholine in plants and humans. Jpn J Pharmacol. 2001;85(1):2–10. doi: 10.1254/jjp.85.2
   PubMedGoogle Scholar
• Tretyn A, Kendrick RE. Acetylcholine in plants: presence, metabolism and mechanism of action. Bot Rev. 1991;57(1):33–73. doi: 10.1007/BF02858764
   Google Scholar
• Matilla MA, Velando F, Tajuelo A, et al. Chemotaxis of the human pathogen Pseudomonas aeruginosa to the neurotransmitter acetylcholine. MBio. 2022;13(2):e03458–21. doi: 10.1128/mbio.03458-21
   Web of Science ®Google Scholar
• Erland LAE, and Saxena PK. In: Sopory S, editor Sens Biol Plants. Singapore:Springer; 2019. p. 411–449. doihttps://doi.org/10.1007/978-981-13-8922-1_16
   Google Scholar
• Chhabra N, Malik C. Influence of spectral quality of light on pollen tube elongation in Arachis hypogaea. Ann Bot. 1978;42(5):1109–1117. doi: 10.1093/oxfordjournals.aob.a085551
   Google Scholar
• Yamamoto K, Oguri S, Momonoki YS. Characterization of trimeric acetylcholinesterase from a legume plant, Macroptilium atropurpureum Urb. Planta. 2008;227(4):809–822. doi: 10.1007/s00425-007-0658-0
   PubMed Web of Science ®Google Scholar
• Hartmann E, Gupta R. 11. Acetylcholine as a signaling system in plants. 1989.
   Google Scholar
• Jia W, Zhang J. Stomatal movements and long-distance signaling in plants. Plant Signal Behav. 2008;3(10):772–777. doi: 10.4161/psb.3.10.6294
   PubMedGoogle Scholar
• Fromm J. Long-distance electrical signaling and physiological functions in higher plants. In: Volkov AG, editor. In Plant electrophysiology: Theory and Methods. Berlin Heidelberg: Springer; 2006. p. 269–285. doi:10.1007/978-3-540-37843-3_12
   Google Scholar
• Horiuchi Y, Kimura R, Kato N, et al. Evolutional study on acetylcholine expression. Life Sci. 2003;72(15):1745–1756. doi: 10.1016/S0024-3205(02)02478-5
   PubMed Web of Science ®Google Scholar
• Kawashima SK, Fujii T. Basic and clinical aspects of non-neuronal acetylcholine: Overview of non-neuronal cholinergic systems and their biological significance. J Pharmacol Sci. 2008;106(2):167–173. doi: 10.1254/jphs.FM0070073
   PubMed Web of Science ®Google Scholar
• Fluck RA, Jaffe MJ. C Cholinesterases from plant tissue: V. Cholinesterase is not pectin esterase. Plant Physiology. 1974;54(5):797–798.
   Web of Science ®Google Scholar
• Hartmann E. Attempts to demonstrate incorporation of labelled precursors into acetylcholine by Phaseolus vulgaris seedlings. Phytochemistry. 1979;18(10):1643–1646. doi: 10.1016/0031-9422(79)80175-2
   Google Scholar
• Roshchina VV, Mukhin EN. Acetylcholine action on the photochemical reactions of pea chloroplasts. Plant Sci. 1985;42(2):95–98. doi: 10.1016/0168-9452(85)90148-7
   Web of Science ®Google Scholar
• Mukherjee A. Computational analysis of a cys-loop ligand gated ion channel from the green alga chlamydomonas reinhardtii. Mol Biol. 2015;49(5):742–754. doi: 10.1134/S002689331505012X
   Web of Science ®Google Scholar
• Beljelarskaya S, Sutton F. Expression of the mammalian serotonin receptor in plant and amphibian cells. Mol Biol. 2003;37(3):387–391. doi: 10.1023/A:1024283126198
   Web of Science ®Google Scholar
• Skirycz A, Świędrych A, Szopa J. Expression of human dopamine receptor in potato (Solanum tuberosum) results in altered tuber carbon metabolism. Bmc Plant Biol. 2005;5(1):1–12. doi: 10.1186/1471-2229-5-1
   Google Scholar
• Roshchina V. Action of acetylcholine agonists and antagonists on reactions of photosynthetic membranes. Photosynthetica (Praha). 1987;21(3):296–300.
   Web of Science ®Google Scholar
• Tretyni A, Bossen M, Kendrick R. Evidence for different types of acetylcholine receptors in plants. In: Progress in Plant Growth Regulation: Proceedings of the 14th International Conference on Plant Growth Substances; 1992 [1991 Jul 21–26]; Amsterdam: Springer.
   Google Scholar
• Bamel K, Gupta R, Gupta SC. Acetylcholine suppresses shoot formation and callusing in leaf explants of in vitro raised seedlings of tomato, Lycopersicon esculentum Miller var. Pusa Ruby. Plant Signal Behav. 2016;11(6):e1187355. doi: 10.1080/15592324.2016.1187355
   Google Scholar
• Bamel K, Gupta R, Gupta SC. Nicotine promotes rooting in leaf explants of in vitro raised seedlings of tomato, Lycopersicon esculentum Miller var. Pusa Ruby. Int Immunopharmacol. 2015;29(1):231–234. doi: 10.1016/j.intimp.2015.09.001
   Web of Science ®Google Scholar
• Di Sansebastiano G-P, Fornaciari S, Barozzi F, et al. New insights on plant cell elongation: a role for acetylcholine. Int J Mol Sci. 2014;15(3):4565–4582. doi: 10.3390/ijms15034565
   Web of Science ®Google Scholar
• Bamel K, Mondal N. In vitro culture using nicotine and d-tubocurarine and in silico analysis depict the presence of acetylcholine receptor (AChR) in tomato (Solanum lycopersicum L.). Vitro Cell Dev Biol Plant. 2023;59(1):39–48. doi: 10.1007/s11627-022-10324-2
   Web of Science ®Google Scholar
• Rotundo RL. Expression and localization of acetylcholinesterase at the neuromuscular junction. J Neurocytol. 2003;32(5–8):743–766. doi: 10.1023/B:NEUR.0000020621.58197.d4
   Google Scholar
• Fluck R, Jaffe M. Cholinesterases from plant tissues VI. Preliminary characterization of enzymes from Solanum melongena L. and Zea mays L. Biochimica et Biophysica Acta (BBA)-Enzymol. 1975;410(1):130–134. doi: 10.1016/0005-2744(75)90213-2
   Google Scholar
• Tretyn A, Foulkesweg G. Acetylcholine in Plants: Presence. Metabolism Forest. 1991;62:275–277.
   Google Scholar
• Wessler I, Kirkpatrick C, Racke K. The cholinergic ‘pitfall’: acetylcholine, a universal cell molecule in biological systems, including humans. Clin Exp Pharma Physio. 1999;26(3):198–205. doi: 10.1046/j.1440-1681.1999.03016.x
   PubMed Web of Science ®Google Scholar
• Momonoki YS. Acetylcholine as a signaling system to environmental stimuli in crops. Jpn J Crop Sci. 1998;67(3):273–283. doi: 10.1626/jcs.67.273
   Google Scholar
• Yamamoto K, Shida S, Honda Y, et al. Overexpression of acetylcholinesterase gene in rice results in enhancement of shoot gravitropism. Biochem Biophys Res Commun. 2015;465(3):488–493. doi: 10.1016/j.bbrc.2015.08.044
   Web of Science ®Google Scholar
• Yamamoto K, Sakamoto H, Momonoki YS. Altered expression of acetylcholinesterase gene in rice results in enhancement or suppression of shoot gravitropism. Plant Signal Behav. 2016;11(4):e1163464. doi: 10.1080/15592324.2016.1163464
   Google Scholar
• Beri V, Gupta R. Acetylcholinesterase inhibitors neostigmine and physostigmine inhibit induction of alpha-amylase activity during seed germination in barley, Hordeum vulgare var. Jyoti. Life Sci. 2007;80(24–25):2386–2388. doi: 10.1016/j.lfs.2007.02.018
   Web of Science ®Google Scholar
• Kasturi R. De novo synthesis of acetylcholinesterase in roots of Pisum sativum. Phytochemistry. 1978;17(4):647–649. doi: 10.1016/S0031-9422(00)94201-8
   Web of Science ®Google Scholar
• Roshchina V, Mukhin E. Acetylcholinesterase activity in chloroplasts and acetylcholine effects on photochemical reactions. 1985.
   Google Scholar
• Raineri M, Modenesi P. Preliminary evidence for a cholinergic-like system in lichen morphogenesis. Histochem J. 1986;18(11–12):647–657. doi: 10.1007/BF01675300
   Google Scholar
• Dettbarn W. Acetylcholinesterase activity in Nitella. Nature. 1962;194(4834):1175–1176. doi: 10.1038/1941175b0
   Web of Science ®Google Scholar
• Sarangle Y, Bamel K, Purty RS. Identification of acetylcholinesterase like gene family and its expression under salinity stress in Solanum lycopersicum. J Plant Growth Regul. 2023;43(3):1–21. doi: 10.1007/s00344-023-11152-3
   Web of Science ®Google Scholar
• Yamamoto K, Oguri S, Chiba S, et al. Molecular cloning of acetylcholinesterase gene from Salicornia europaea L. Plant Signal Behav. 2009;4(5):361–366. doi: 10.4161/psb.4.5.8360
   PubMedGoogle Scholar
• Sagane Y, Nakagawa T, Yamamoto K, et al. Molecular characterization of maize acetylcholinesterase. A novel enzyme family in the plant kingdom. Plant Physiol. 2005;138(3):1359–1371. doi: 10.1104/pp.105.062927
   Web of Science ®Google Scholar
• Riov J, Jaffe M. Cholinesterases from plant tissues: I. Purification and characterization of a cholinesterase from mung bean roots. Plant Physiol. 1973;51(3):520–528. doi: 10.1104/pp.51.3.520
   Web of Science ®Google Scholar
• Sagane Y, Nakagawa T, Yamamoto K, et al. Molecular characterization of maize acetylcholinesterase: a novel enzyme family in the plant kingdom. Plant Physiol. 2005;138(3):1359–1371. doi: 10.1104/pp.105.062927
   Web of Science ®Google Scholar
• Shen G, Sun W, Chen Z, et al. Plant GDSL esterases/lipases: Evolutionary, physiological and molecular functions in plant development. Plants. 2022;11(4). doi: 10.3390/plants11040468
   Google Scholar
• Muralidharan M, Buss K, Larrimore KE, et al. The Arabidopsis thaliana ortholog of a purported maize cholinesterase gene encodes a GDSL-lipase. Plant Mol Biol. 2013;81(6):565–576. doi: 10.1007/s11103-013-0021-8
   Web of Science ®Google Scholar
• Akoh CC, Lee G-C, Liaw Y-C, et al. GDSL family of serine esterases/lipases. Progress Lipid Res. 2004;43(6):534–552. doi: 10.1016/j.plipres.2004.09.002
   PubMed Web of Science ®Google Scholar
• Fluck R, Jaffe M. Cholinesterases from plant tissues: III. Distribution and subcellular localization in Phaseolus aureus Roxb. Plant Physiol. 1974;53(5):752–758. doi: 10.1104/pp.53.5.752
   Web of Science ®Google Scholar
• Yamamoto K, Momonoki YS. Subcellular localization of overexpressed maize AChE gene in rice plant. Plant Signal Behav. 2008;3(8):576–577. doi: 10.4161/psb.3.8.5732
   PubMedGoogle Scholar
• Fluck R, Jaffe M. The distribution of cholinesterases in plant species. Phytochemistry. 1974;13(11):2475–2480. doi: 10.1016/S0031-9422(00)86923-X
   Web of Science ®Google Scholar
• Franzoni G, Trivellini A, Bulgari R, et al. Bioactive molecules as regulatory signals in plant responses to abiotic stresses. In: Khan MIR, editor. Plant Signaling Molecules: Role and Regulation Under Stressful Environments. Cambridge United Kingdom: Elsevier; 2019. p. 169–182.
   Google Scholar
• Erland LAE, Saxena PK. Beyond a neurotransmitter: the role of serotonin in plants. Neurotransmitter. 2017;4(5):1–12.
   Google Scholar
• Qin C, Ahanger MA, Lin B, et al. Comparative transcriptome analysis reveals the regulatory effects of acetylcholine on salt tolerance of Nicotiana benthamiana. Phytochemistry. 2021;181:112582. doi: 10.1016/j.phytochem.2020.112582
   PubMed Web of Science ®Google Scholar
• Braga-Reis I, Neris DM, Ribas AF, et al. Gamma-aminobutyric acid (GABA) and acetylcholine (ACh) alleviate water deficit effects in soybean: From gene expression up to growth performance. Environ Exp Bot. 2021;182:104303. doi: 10.1016/j.envexpbot.2020.104303
   Web of Science ®Google Scholar
• Qi M, Zheng X, Niu G, et al. Supplementation of acetylcholine mediates physiological and biochemical changes in tobacco lead to alleviation of damaging effects of drought stress on growth and photosynthesis. J Plant Growth Regul. 2023;42(8):4616–4628. doi: 10.1007/s00344-022-10642-0
   Web of Science ®Google Scholar
• Su Y, Qin C, Begum N, et al. Acetylcholine ameliorates the adverse effects of cadmium stress through mediating growth, photosynthetic activity and subcellular distribution of cadmium in tobacco (Nicotiana benthamiana). Ecotoxicol Environ Saf. 2020;198:110671. doi: 10.1016/j.ecoenv.2020.110671
   PubMed Web of Science ®Google Scholar
• Momonoki YS, Momonoki T. Changes in acetylcholine levels following leaf wilting and leaf recovery by heat stress in plant cultivars. Jpn J Crop Sci. 1991;60(2):283–290.
   Google Scholar
• Momonoki YS, Oguri S, Kato S, et al. Studies on the mechanism of salt tolerance in Salicornia europaea L.: III, Salt accumulation and ACh function. Jpn J Crop Sci. 1996;65(4):693–699.
   Google Scholar
• Momonoki YS, Momonoki T, Whallon JH. Acetylcholine as a signaling system to environmental stimuli in plants: I. Contribution of Ca2+ in heat-stressed Zea mays seedlings. Jpn J Crop Sci. 1996;65(2):260–268.
   Google Scholar
• Yamamoto K, Sakamoto H, Momonoki YS. Maize acetylcholinesterase is a positive regulator of heat tolerance in plants. J Plant Physiol. 2011;168(16):1987–1992. doi: 10.1016/j.jplph.2011.06.001
   Web of Science ®Google Scholar
• Momonoki YS, Momonoki T. Changes in acetylcholine-hydrolyzing activity in heat-stressed plant cultivars. Jpn J Crop Sci. 1993;62(3):438–446.
   Google Scholar
• Momonoki YS, Momonoki T. The influence of heat stress on acetylcholine content and its hydrolyzing activity in Macroptilium atropurpureum cv. Siratro. Jap J Crop Sci. 1992;61(1):112–118.
   Google Scholar
• Sarangle Y, Bamel K, Purty RS. Identification of acetylcholinesterase like gene family and its expression under salinity stress in Solanum lycopersicum. J Plant Growth Regul. 2024;43(3):940–960. doi: 10.1007/s00344-023-11152-3
   Web of Science ®Google Scholar
• Madhavan S, Sarath G, Lee BH, et al. Guard cell protoplasts contain acetylcholinesterase activity. Plant Sci. 1995;109(2):119–127. doi: 10.1016/0168-9452(95)04164-P
   Web of Science ®Google Scholar
• Wang H, Wang X, Zhang S, et al. Nicotinic acetylcholine receptor is involved in acetylcholine regulating stomatal movement. Sci China Ser Life Sci. 1998;41(6):650–656. doi: 10.1007/BF02882908
   Web of Science ®Google Scholar
• Meng F, Liu X, Zhang S, et al. Localization of muscarinic acetylcholine receptor in plant guard cells. Chin Sci Bull. 2001;46(7):586–587. doi: 10.1007/BF02900416
   Google Scholar
• Roychoudhury A. Neurotransmitter acetylcholine comes to the plant rescue. J Mol Cell Biol Forecast. 2020;3(1):1019.
   Google Scholar
• Shen J, Qin C, Qin Y, et al. Acetylcholine alleviates salt stress in Zea mays L. by promoting seed germination and regulating phytohormone level and antioxidant capacity. J Plant Growth Regul. 2023;43(1):1–12. doi: 10.1007/s00344-023-11089-7
   Web of Science ®Google Scholar
• Qin C, Ahanger MA, Zhou J, et al. Beneficial role of acetylcholine in chlorophyll metabolism and photosynthetic gas exchange in Nicotiana benthamiana seedlings under salinity stress. Plant Biol J. 2020;22(3):357–365. doi: 10.1111/plb.13079
   Web of Science ®Google Scholar
• Qi M, Zheng X, Niu G, et al. Supplementation of acetylcholine mediates physiological and biochemical changes in tobacco lead to alleviation of damaging effects of drought stress on growth and photosynthesis. J Plant Growth Regul. 2022;42(8):4616–4628. doi: 10.1007/s00344-022-10642-0
   Web of Science ®Google Scholar
• Qin C, Ahanger MA, Zhou J, et al. Beneficial role of acetylcholine in chlorophyll metabolism and photosynthetic gas exchange in Nicotiana benthamiana seedlings under salinity stress. Plant Biol (Stuttg). 2020;22(3):357–365. doi: 10.1111/plb.13079
   Web of Science ®Google Scholar
• Yamamoto K, Momonoki YS. Tissue localization of maize acetylcholinesterase associated with heat tolerance in plants. Plant Signal Behav. 2012;7(3):301–305. doi: 10.4161/psb.19007
   PubMedGoogle Scholar
• Momonoki YS. Occurrence of acetylcholine-hydrolyzing activity at the stele-cortex interface. Plant Physiol. 1992;99(1):130–133. doi: 10.1104/pp.99.1.130
   Web of Science ®Google Scholar
• Bita CE, Gerats T. Plant tolerance to high temperature in a changing environment: scientific fundamentals and production of heat stress-tolerant crops. Front Plant Sci. 2013;4:273. doi: 10.3389/fpls.2013.00273
   PubMed Web of Science ®Google Scholar
• Roshchina V, Yashin V. Secreting cells of Saintpaulia as a model for studies of plant cholinergic system. Biologicheskie Membrany. 2013;30(5–6):454–461.
   Web of Science ®Google Scholar
• Roshchina V, Yashin, VA, Švirst, NA, et al. Secreting cells as models to study the role of acetylcholine in signalling and communications of organisms. In: Zinchenko VP, Berezhnov AV, editors. The book of international conference “reception and intracellular signaling; 27–30 May 2013; EMA Pushchino; 2013. Vol. 2. p. 790–795
   Google Scholar
• Roshchina VAV. Model systems to study the excretory function of higher plants. Springer Dordrecht: Springer; 2014.
   Google Scholar
• Michelson MJ, Zeimal EV. Acetylcholine: an approach to the molecular mechanism of action. 1st ed. Oxford: Pergammon Press; 1973.
   Google Scholar
• Kennedy DO. Plants and the human brain. USA: Oxford University Press; 2014.
   Google Scholar
• Malik S. Cholinesterases in animals and Arabidopsis Thaliana. Int J Innovative Res Dev. 2014;3(2):280–281.
   Google Scholar
• Wessler I, Michel-Schmidt R, Kirkpatrick CJ. pH-dependent hydrolysis of acetylcholine: Consequences for non-neuronal acetylcholine. Int Immunopharmacol. 2015;29(1):27–30. doi: 10.1016/j.intimp.2015.04.039
   Web of Science ®Google Scholar
• Roshchina VV. The fluorescence methods to study neurotransmitters (Biomediators) in plant cells. J Fluoresc. 2016;26(3):1029–1043. doi: 10.1007/s10895-016-1791-6
   Web of Science ®Google Scholar
• Roshchina VV. New Trends and Perspectives in the Evolution of Neurotransmitters in Microbial, Plant, and Animal Cells. In: Lyte M, editor. Microbial Endocrinology: Interkingdom Signaling in Infectious Disease and Health. Advances in Experimental Medicine and Biology. Springer Cham: Springer; 2016. Vol. 874. p. 25–77.
   Google Scholar
• Fillafer C, Schneider MF. On the excitation of action potentials by protons and its potential implications for cholinergic transmission. Protoplasma. 2016;253(2):357–365. doi: 10.1007/s00709-015-0815-4
   Web of Science ®Google Scholar
• Roshchina V, Shvirst N. Cholinesterase in contractile structures of plants and animals: histochemical experiments with azocompounds. In Biological Motility Ed Udaltsov SN Materials of International Symposium. Pushchino: SYNCHROBOOK; 2016. p. 198–202.
   Google Scholar
• Amaroli A. Neurotransmitters or Biomediators. Cholinergic Syst Protozoa EC Microbiol. 2017;7:40–41.
   Google Scholar
• Ramakrishna A, Roshchina VV. Neurotransmitters in plants: perspectives and applications. Boca Raton: CRC Press, Taylor & Francis; 2018. doi:10.1201/b22467
   Google Scholar
• Roshchina V. Cholinesterase in secreting cells and isolated organelles of plants. Biologicheskie Membrany. 2018;35(2):143–149.
   Web of Science ®Google Scholar
• Kurchii BA. Possible participation of acetylcholine in free-radical processes (redox reactions) in living cells. In: Ramakrishna A, Roshchina V, editors. Neurotransmitters in Plants: Perspectives and Applications. Boca Raton:: CRC Press, Taylor & Francis; 2018. p. 211–217.
   Google Scholar
• Roshchina VV. Inter-and intracellular signaling in plant cells with participation of neurotransmitters (Biomediators). In: Ramakrishna A, and Roshchina V, editors. Neurotransmitters in Plants: perspectives and Applications. Boca Raton: CRC Press, Taylor & Francis; 2018. p. 147–180.
   Google Scholar
• Roshchina V. Tools for microanalysis of the neurotransmitter location in plant cells. Neurotransmitters in plants, perspectives and applications. Boca Raton: CRC Press; 2018. p. 135–146.
   Google Scholar
• Yang L, Ma X, Guo Y, et al. Acetylcholine (ACh) enhances Cd tolerance through transporting ACh in vesicles and modifying Cd absorption in duckweed (Lemna turionifera 5511). Environ Pollut. 2023;335:122305. doi: 10.1016/j.envpol.2023.122305
   Web of Science ®Google Scholar