Triticum aestivum
|
|
4 °C for 1 and 12 h |
Up-regulated the expression of TaCYP710A1; increased the content of stigmasterol |
[80] |
Lactuca sativa
|
|
35 or 21 °C for 40 h |
Up-regulated the concentrations of sterols |
[81] |
Helianthus annuus
|
|
25 or 35 °C for 1–5 days |
Reduced the level of stigmasterol |
[82] |
Phaeodactylum tricornutum
|
|
13 or 23 °C under white light |
Reduced the level of the total sterols at 23 °C |
[83] |
Avena sativa
|
|
2 °C for 4 weeks |
Increased acylated sterol glycoside (ASG) content; changes in the ratio of free sterol and ASG |
[84] |
Arabidopsis thaliana
|
|
7 ± 1 ℃ for 30 days |
Increased the permeability of plant cell membrane; increased ratio of stigmasterol to sitosterol |
[85] |
Arabidopsis thaliana
|
|
45 ℃ for 3 and 6 h |
Increased fatality rate |
[85] |
Arabidopsis thaliana
|
AtCYP710A1 gene-overexpression |
45 ℃ for 3 and 6 h |
Enhanced the heat tolerance and reduced the mortality |
[85] |
Triticum aestivum
|
|
4 ℃ for 1 and 12 h |
Destructed membrane integrity; accumulated reactive oxygen species; increased total sterol content; increased the ratio of C24-methy sterol and C24-ethyl sterol |
[86] |
Triticum aestivum
|
5 mM MβCD for 12 h |
4 ℃ for 1 and 12 h |
Decreased sterol content; aggravated the cold stress injury |
[86] |
Lycopersicon esculentum
|
Seeds were soaked with 10 μM sitosterol for 10 h |
10, 25, and 45 ± 3 °C for 14 days |
Increased tolerance of tomato plants to both high and low temperature stress |
[87] |
Agrostis stolonifera
|
400 μM sitosterol, foliar spraying until droplets formed |
35 °C for 28 days |
Inhibited the leaf senescence under heat stress; enhanced plant heat tolerance. |
[88] |
Glycine max
|
|
25 mM NaCl for 8 days |
Decreased the content of total sterols by 50%; increased the content of saturated fatty acids |
[89] |
Kosteletzkya virginica
|
|
85 mM NaCl for 17–20 days |
Decreased the content of total sterol |
[90] |
Brassica oleracea
|
|
0, 40 and 80 mM NaCl for 15 days |
Decreased the content of sitosterol; increased stigmasterol content |
[91] |
Zea mays
|
|
150 mM NaCl for 15 days |
Decreased the content of total sterol |
[92] |
Spartina patens
|
|
0, 170, 340, and 510 mM NaCl for 10 weeks |
Decreased sitosterol in response to elevated NaCl. |
[93] |
Triticum aestivum
|
|
150 mM NaCl for 21 days |
Decreased the content of campesterol and cholesterol; improved salt tolerance |
[94] |
Lycopersicon esculentum
|
|
50 and 100 mM NaCl for 4 weeks |
Increased the ratio of sterols and phospholipids; enhanced salt tolerance; improved membrane rigidity |
[95] |
Nicotiana tabacum
|
Overexpressing AaSMO1
|
400 mM NaCl for 0, 0.5, 1.5, 3, 6, 9, 24 and 72 h |
Decreased the sensitivity of plants to dehydration stress; increased the content of total sterols |
[96] |
Brassica oleracea, Brassica napus and Cakile maritima
|
|
100 and 200 mM NaCl for 1 week |
Increased the level of stigmasterol; enhanced the adaption of the membrane to salt stress |
[97] |
Linum usitatissimum
|
seeds were soaked with 200 ppm stigmasterol for 12 h |
0, 100, 150 or 200 mM NaCl for 40 days |
Decreased the drastic affect by NaCl; enhanced plant salinity tolerance |
[98] |
Capsicum annuum
|
150 ppm sitosterol |
50, 100 or 200 mM NaCl |
Offset the salinity stress damage; improved membrane stability and antioxidant enzyme activity |
[99] |
Vitis vinifera
|
|
UV-B (8.25 lW·cm−2, 16 h) |
Increased the content of sitosterol and stigmasterol |
[100] |
Vitis vinifera
|
|
UV-B (33 lW·cm−2, 4 h) |
Increased the content of triterpenoids 4.8-fold |
[100] |
Olea europaea
|
|
UV-B (6.5 kJ·m−2·day−1, 5 days) |
No significant influence on the content of sterol |
[101] |
Olea europaea
|
|
UV-B (12.4 kJ·m−2·day−1, 5 days) |
No significant influence on the content of sterol |
[101] |
Withania somnifera
|
|
UV-B (3.6 kJ·m−2·day−1) |
Decreased the content of triterpenoids in leaf; increased triterpenoids levels in root |
[102] |
Oryza sativa
|
150 μM sitosterol for 20 days |
UV-B (315 ± 20 nm, 6 h per day, 5 days) |
Improved the growth of rice plants; enhanced tolerance of rice to UV-B stress |
[103] |
Oryza sativa
|
|
Water stress for 3, 6, 9 and 12 days |
Up-regulated the level of stigmasterol, campesterol, β-sitosterol; decreased the activity of HMGR in rice |
[104] |
Cucurbita pepo
|
|
Five levels of drought stress on seed |
Increased the content of plant sterols, especially β-sitosterol; inhibited the oil production of pumpkin seeds |
[105] |
Oryza sativa
|
|
Drought stress for 3, 6, 9 and 12 days |
Increased the content of both free sterols and sterol ester; improved HMGR activity |
[106] |
Camellia sinensis
|
|
1, 8, and 15 days under water deprivation treatment |
Increased sterols levels |
[107] |
Cynodon dactylon
|
smt1 mutant |
Drought stress for 7 days |
Increased the content of cholesterol, putrescine (Put), spermidine (Spd), and spermine (Spm); improved drought tolerance |
[68] |
Oryza sativa
|
Knock-down of OsSMT1 expression by RNA interference |
Drought stress for 7 days |
Increased the content of cholesterol, Put, Spd, and Spm; improved drought tolerance |
[68] |
Trifolium repens
|
120 μM sitosterol for 3 days |
Drought stress for 7 days |
Enhanced the drought tolerance and total antioxidant capacity. |
[108] |
Triticum aestivum
|
0, 25, 50, 100 mg·L−1 sitosterolapplied to wheat plants foliage |
50% of crop evapotranspiration for 45 days |
Offset the damage caused by drought to plants; improved yield. |
[109] |