Professional Documents
Culture Documents
2
ﻣﺤﻤﺪ ﻣﻬﺮﮔﺎن ،1ﻋﻠﻲ ﻣﻬﺮآﻓﺮﻳﻦ ،2ﻣﺤﻤﺪرﺿﺎ ﻟﺒﺎﻓﻲ ،⃰ 2ﺣﺴﻨﻌﻠﻲ ﻧﻘﺪيﺑﺎدي
-1داﻧﺸﺠﻮي ﻛﺎرﺷﻨﺎﺳﻲ ارﺷﺪ ،داﻧﺸﮕﺎه آزاد اﺳﻼﻣﻲ واﺣﺪ ﻋﻠﻮم ﺗﺤﻘﻴﻘﺎت ﺗﻬﺮان ،ﺗﻬﺮان ،اﻳﺮان
-2ﻣﺮﻛﺰ ﺗﺤﻘﻴﻘﺎت ﮔﻴﺎﻫﺎن داروﻳﻲ ،ﭘﮋوﻫﺸﻜﺪه ﮔﻴﺎﻫﺎن داروﻳﻲ ﺟﻬﺎدداﻧﺸﮕﺎﻫﻲ ،ﻛﺮج ،اﻳﺮان
⃰ آدرس ﻣﻜﺎﺗﺒﻪ :ﻛﺮج ،ﭘﮋوﻫﺸﻜﺪه ﮔﻴﺎﻫﺎن داروﻳﻲ ﺟﻬﺎد داﻧﺸﮕﺎﻫﻲ ،ﺻﻨﺪوقﭘﺴﺘﻲ31375 - 1369 :
ﺗﻠﻔﻦ ،(026) 34764010-19 :ﻧﻤﺎﺑﺮ(026) 34764021 :
ﭘﺴﺖ اﻟﻜﺘﺮوﻧﻴﻚMohammad1700@yahoo.com :
روش ﺑﺮرﺳﻲ :آزﻣﺎﻳﺶ در ﻗﺎﻟﺐ ﻃﺮح ﺑﻠﻮك ﻛﺎﻣﻞ ﺗﺼﺎدﻓﻲ ﺑﺎ ﺳﻪ ﺗﻜﺮار در ﺷﺮاﻳﻂ ﮔﻠﺨﺎﻧﻪاي ﺑﺎ ﺗﻴﻤﺎر ﻛﻴﺘﻮزان ،در ﭼﻬﺎر ﺳﻄﺢ
ﺷﺎﻣﻞ 0/1 ،0/05 ،0و 0/2درﺻﺪ اﻧﺠﺎم ﺷﺪ.
ﻧﺘﺎﻳﺞ :ﻧﺘﺎﻳﺞ ﺑﻪ دﺳﺖ آﻣﺪه از ﺗﺠﺰﻳﻪ وارﻳﺎﻧﺲ دادهﻫﺎ ﻧﺸﺎن داد ،ﻛﻪ ﻣﺤﻠﻮلﭘﺎﺷﻲ ﻣﺤﺮكزﻳﺴﺘﻲ ﻛﻴﺘﻮزان اﺛﺮ ﻣﻌﻨﻲداري ﺑﺮ وزن ﺧﺸﻚ
ﺑﺮگ ،وزن ﺧﺸﻚ اﻧﺪام ﻫﻮاﻳﻲ ،ﻃﻮل ﺑﺮگ ) ،(P<0/05ﻓﻨﻞ و رﺑﺎدﻳﻮزﻳﺪ (P<0/01) Aداﺷﺘﻪ اﺳﺖ .ﻛﻴﺘﻮزان در ﺳﻄﺢ 0/1درﺻﺪ
ﺑﻴﺸﺘﺮﻳﻦ وزن ﺗﺮ و ﺧﺸﻚ ﺳﺎﻗﻪ ،ﺑﺮگ و اﻧﺪام ﻫﻮاﻳﻲ را ﺗﻮﻟﻴﺪ ﻧﻤﻮد ،ﺑﻪ ﻃﻮري ﻛﻪ ﺑﺎ اﻓﺰاﻳﺶ ﻏﻠﻈﺖ ﻛﻴﺘﻮزان از 0/1ﺑﻪ 0/2درﺻﺪ اﻳﻦ
ﺻﻔﺎت ﻛﺎﻫﺶ ﻳﺎﻓﺖ .ﺑﻴﺸﺘﺮﻳﻦ ﻣﻴﺰان ﻓﻨﻞ در ﻏﻠﻈﺖ 0/1درﺻﺪ ﻛﻴﺘﻮزان ﻣﺸﺎﻫﺪه ﺷﺪ ،ﻫﻤﭽﻨﻴﻦ در اﻳﻦ آزﻣﺎﻳﺶ ﻛﻴﺘﻮزان ﺑﺎ ﻏﻠﻈﺖ 0/2
درﺻﺪ ﺑﻴﺸﺘﺮﻳﻦ ﺗﺎﺛﻴﺮ را ﺑﺮ رﺑﺎدﻳﻮزﻳﺪ Aداﺷﺘﻪ اﺳﺖ.
ﻧﺘﻴﺠﻪﮔﻴﺮي :ﻣﺤﻠﻮلﭘﺎﺷﻲ ﻛﻴﺘﻮزان ﺳﺒﺐ ﺑﻬﺒﻮد ﺧﺼﻮﺻﻴﺎت ﺑﻴﻮﻣﺎس روﻳﺸﻲ و ﺻﻔﺎت ﺑﻴﻮﺷﻴﻤﻴﺎﻳﻲ ﻣﺎﻧﻨﺪ رﺑﺎدﻳﻮزﻳﺪ Aﮔﻴﺎه اﺳﺘﻮﻳﺎ ﺷﺪه اﺳﺖ.
169
ﺳﺎل ﺷﺎﻧﺰدﻫﻢ ،دوره دوم ،ﺷﻤﺎره ﻣﺴﻠﺴﻞ ﺷﺼﺖ و دوم ،ﺑﻬﺎر 1396
اﺛﺮ ﻏﻠﻈﺖﻫﺎي ﻣﺨﺘﻠﻒ ﻣﺤﺮك ...
170
ﻣﻬﺮﮔﺎن و ﻫﻤﻜﺎران
اﻧﺪازهﮔﻴﺮي ﺷﺪ .اﻳﻦ دﺳﺘﮕﺎه ﺑﺪون آﺳﻴﺐ ﺑﻪ ﺳﺎﺧﺘﺎر ﺑﺮگ ﻣﻴﺰان ﻣﻮاد و روشﻫﺎ
ﺳﺒﺰﻳﻨﮕﻲ ﺑﺮگ را اﻧﺪازهﮔﻴﺮي ﻛﺮده و ﺑﻪ ﺻﻮرت ﻋﺪد ﻧﻤﺎﻳﺶ ﻣﻲدﻫﺪ. ﺑﻪ ﻣﻨﻈﻮر ﺑﺮرﺳﻲ اﺛﺮ ﻣﺤﺮك زﻳﺴﺘﻲ ﻛﻴﺘﻮزان ﺑﺮ ﺧﺼﻮﺻﻴﺎت
ﺑﻴﻮﺷﻴﻤﻴﺎﻳﻲ و ﻣﻮرﻓﻮﻓﻴﺰﻳﻮﻟﻮژﻳﻜﻲ آزﻣﺎﻳﺸﻲ در ﻗﺎﻟﺐ ﺑﻠﻮكﻫﺎي
اﻧﺪازهﮔﻴﺮي رﺑﺎدﻳﻮزﻳﺪ Aﺑﻪ روش ﻛﺮوﻣﺎﺗﻮﮔﺮاﻓﻲ ﻣﺎﻳﻊ ﺑﺎ ﻛﺎﻣﻞ ﺗﺼﺎدﻓﻲ ﺑﺎ ﺳﻪ ﺗﻜﺮار در ﺳﺎل زراﻋﻲ 94در ﮔﻠﺨﺎﻧﻪ ﺗﺤﻘﻴﻘﺎﺗﻲ
(High-performance liquid ﺑﺎﻻ ﻛﺎراﻳﻲ ﭘﮋوﻫﺸﻜﺪه ﮔﻴﺎﻫﺎن داروﻳﻲ ﺟﻬﺎد داﻧﺸﮕﺎﻫﻲ واﻗﻊ در ﻫﻠﺠﺮد ﻛﺮج
)(HPLC) chromatography اﻧﺠﺎم ﺷﺪ ﻛﻪ در اﻳﻦ آزﻣﺎﻳﺶ ﻣﺤﺮك زﻳﺴﺘﻲ ﻛﻴﺘﻮزان در 4ﺳﻄﺢ
ﺑﻪ ﻣﻨﻈﻮر اﻧﺪازهﮔﻴﺮي و رﺑﺎدﻳﻮزﻳﺪ Aاﺑﺘﺪا ﻣﻘﺪار 0/2ﮔﺮم از ) 0/1 ،0/05 ،0و 0/2درﺻﺪ( ﻣﻮرد ارزﻳﺎﺑﻲ ﻗﺮار ﮔﺮﻓﺖ.
ﺑﺎﻓﺖ ﺑﺮگ ﺧﺸﻚ ﮔﻴﺎه را در ﻫﺎون ﭼﻴﻨﻲ ﺳﺎﻳﻴﺪه و ﻣﻘﺪار 25 واﺣﺪﻫﺎي آزﻣﺎﻳﺸﻲ ﺷﺎﻣﻞ ﮔﻠﺪانﻫﺎي ﭘﻼﺳﺘﻴﻜﻲ ﺑﺎ ﻗﻄﺮ 30
ﻣﻴﻠﻲﻟﻴﺘﺮ ﻣﺨﻠﻮط 7ﺣﺠﻢ آب و 3ﺣﺠﻢ اﺳﺘﻮﻧﻴﺘﺮﻳﻞ ﺑﻪ آن اﻓﺰوده و ﺳﺎﻧﺘﻲﻣﺘﺮ و ارﺗﻔﺎع 22ﺳﺎﻧﺘﻲﻣﺘﺮ ﺑﻪ ﻫﻤﺮاه زﻫﻜﺶ ﻣﻨﺎﺳﺐ ﺟﻬﺖ
ورﺗﻜﺲ ﺷﺪ ﺳﭙﺲ ﺑﻪ ﻣﺪت 60دﻗﻴﻘﻪ ﺑﺎ اﺳﺘﻔﺎده از دﺳﺘﮕﺎه ﺟﻠﻮﮔﻴﺮي از ﺗﺠﻤﻊ آب در ﺗﻪ ﮔﻠﺪان ﺑﺎ ﺧﺎك اﻟﻚ ﺷﺪه و
اوﻟﺘﺮاﺳﻮﻧﻴﻚ اﺳﺘﺨﺮاج اﻧﺠﺎم ﮔﺮﻓﺖ و در ﭘﺎﻳﺎن ﺑﻪ ﻣﺪت ﭼﻬﺎر دﻗﻴﻘﻪ ﻳﻜﻨﻮاﺧﺖ ﺷﺎﻣﻞ ﺧﺎك ﺑﺎﻏﭽﻪ ،رس و ﻣﺎﺳﻪ ﺑﻪ ﻧﺴﺒﺖ ﻣﺴﺎوي ﭘﺮ
ﺑﺎ ﺳﺮﻋﺖ 5000دور ﺑﺮ دﻗﻴﻘﻪ ﺳﺎﻧﺘﺮﻳﻔﻴﻮژ ﺷﺪ .ﺳﭙﺲ ﻣﺤﻠﻮل روﻳﻲ ﺷﺪ .ﺳﭙﺲ در ﻫﺮ ﮔﻠﺪان 2ﻧﺸﺎي ﻳﻜﺴﺎن و ﻫﻢاﻧﺪازه اﺳﺘﻮﻳﺎ
ﺑﻪ ﻧﺴﺒﺖ 1ﺑﻪ 10ﺑﺎ ﻓﺎز ﻣﺘﺤﺮك HPLCرﻗﻴﻖ ﺷﺪ و ﭘﺲ از ﻋﺒﻮر ﻛﺸﺖ ﺷﺪ .ﮔﻠﺪانﻫﺎ ﺗﺎ اﺳﺘﻘﺮار ﻛﺎﻣﻞ ﻧﺸﺎﻫﺎ ﺑﻪ ﺻﻮرت ﻳﻚ روز
از ﻓﻴﻠﺘﺮ ﺳﺮﺳﺮﻧﮕﻲ 0/45 µmﺟﻬﺖ آﻧﺎﻟﻴﺰ HPLCﻣﻮرد اﺳﺘﻔﺎده درﻣﻴﺎن و ﺑﺎ آب ﻣﻌﻤﻮﻟﻲ آﺑﻴﺎري ﺷﺪﻧﺪ .ﺑﻪ ﻣﻨﻈﻮر اﺳﺘﻘﺮار ﻛﺎﻣﻞ
ﻗﺮار ﮔﺮﻓﺖ )اﺳﺘﺎﻧﺪارد ﻣﻠﻲ اﻳﺮان .(16878 ،در روش ﮔﻴﺎﻫﺎن و اﻋﻤﺎل ﺗﻴﻤﺎرﻫﺎ ﭘﺲ از ﮔﺬﺷﺖ 70روز از ﻛﺎﺷﺖ
ﻛﺮوﻣﺎﺗﻮﮔﺮاﻓﻲ ﻣﺎﻳﻊ ﺑﺎ ﻛﺎراﻳﻲ ﺑﺎﻻ ﺟﺪاﺳﺎزي ﺑﺮ ﭘﺎﻳﻪ ﺗﻔﺎوت ﻗﻄﺒﻴﺖ ﺗﻴﻤﺎرﻫﺎي ﻣﺤﻠﻮل ﭘﺎﺷﻲ ﻛﻴﺘﻮزان اﻧﺠﺎم ﺷﺪ .ﺗﻴﻤﺎرﻫﺎي
ﻣﺎده ﻣﻮرد ﺟﺪاﺳﺎزي در دو ﻓﺎز ﺳﺎﻛﻦ و ﻣﺘﺤﺮك اﻧﺠﺎم ﻣﻲﺷﻮد. ﻣﺤﻠﻮلﭘﺎﺷﻲ ﻛﻴﺘﻮزان در ﺳﺎﻋﺖ اوﻟﻴﻪ روز و ﻃﻲ ﺳﻪ دوره ﺑﻪ
ﻣﺤﻠﻮل اﺳﺘﺎﻧﺪارد رﺑﻮدﻳﻮزﻳﺪ Aﺳﻴﮕﻤﺎ ﺑﻪ ﺷﻤﺎره 01432ﺑﺮاي ﻓﺎﺻﻠﻪ ﻳﻚ روز درﻣﻴﺎن ﺑﻪ ﺻﻮرت ﺑﺮﮔﻲ ﺑﻪ ﻧﺤﻮي ﻛﻪ ﺳﻄﺢ
اﻧﺪازهﮔﻴﺮي ﻣﻴﺰان رﺑﻮدﻳﻮزﻳﺪ Aﻣﻮرد اﺳﺘﻔﺎده ﻗﺮار ﮔﺮﻓﺖ .ﻓﺎز ﺑﺮگ ﻣﺮﻃﻮب ﺷﻮد ،اﻧﺠﺎم ﺷﺪ و ﺑﺮاي ﺗﻬﻴﻪ ﻣﺤﻠﻮل ﻛﻴﺘﻮزان
ﺳﺎﻛﻦ ﺳﺘﻮنﻫﺎي HPLCاز ﺟﻨﺲ ﻓﻮﻻد ﺿﺪزﻧﮓ ﻳﺎ ﺷﻴﺸﻪ و ﻓﺎز )ﺷﺮﻛﺖ Sigma-Aldrichآﻣﺮﻳﻜﺎ( ﺑﺎ وزن ﻣﻮﻟﻜﻮﻟﻲ ﭘﺎﻳﻴﻦ از
ﻣﺘﺤﺮك ﺗﺮﻛﻴﺒﻲ از ﺣﻼلﻫﺎي ﻗﻄﺒﻲ )اﻟﻜﻞ( و ﻏﻴﺮﻗﻄﺒﻲ اﺳﻴﺪ اﺳﺘﻴﻚ ﺟﻬﺖ ﺣﻼل و از آب ﻣﻘﻄﺮ ﺑﺮاي رﻗﻴﻖ ﻛﺮدن
)ﻫﻴﺪروﻛﺮﺑﻦ( ﻣﻲﺑﺎﺷﺪ و ﺑﺎ ﺗﻐﻴﻴﺮ ﺣﻼلﻫﺎي )ﻗﻄﺒﻴﺖ( ﻓﺎز ﻣﺘﺤﺮك، اﺳﺘﻔﺎده ﺷﺪ .ﺑﺎ ﺗﻮﺟﻪ ﺑﻪ اﻳﻦ ﻛﻪ ﺑﻬﺘﺮﻳﻦ زﻣﺎن ﻣﺤﻠﻮلﭘﺎﺷﻲ ﺑﻮﺗﻪﻫﺎ
اﺟﺰاي ﻧﻤﻮﻧﻪ از ﻫﻢ ﺟﺪا ﻣﻲﺷﻮد .دﺳﺘﮕﺎه HPLCﻣﻮرد اﺳﺘﻔﺎده در ﺳﺎﻋﺖ اوﻟﻴﻪ روز ﻣﻲﺑﺎﺷﺪ ،ﻫﻤﻪ ﺗﻴﻤﺎرﻫﺎ در اﻳﻦ زﻣﺎن ﺑﻪ ﺻﻮرت
اﻳﻦ آزﻣﺎﻳﺶ از HPLCﻣﺪل ،KNAUERﻧﻮع ﺳﺘﻮن ﻳﻜﺴﺎن اﻋﻤﺎل ﺷﺪ .در ﭘﺎﻳﺎن اﻳﻦ ﻣﺮﺣﻠﻪ وزن ﺗﺮ و ﺧﺸﻚ ﺑﺮگ،
،LICHROSPHER 100 NH2 5µm 25×0.46 cmﻣﺪل وزن ﺗﺮ و ﺧﺸﻚ ﺳﺎﻗﻪ ،وزن ﺗﺮ و ﺧﺸﻚ اﻧﺪام ﻫﻮاﻳﻲ ،وزن ﺗﺮ
ﭘﻤﭗ ] ،[KNAUER- K1001ﻣﺪل دﺗﻜﺘﻮر [KNAUER-UV و ﺧﺸﻚ رﻳﺸﻪ ،ﺷﺎﺧﺺ ﺳﺒﺰﻳﻨﮕﻲ ﺑﺮگ ) ،(SPADﻃﻮل و
،(K2501)] 210 nmﺳﺮﻋﺖ ﺟﺮﻳﺎن 1 ml/minو ﻓﺎز ﻣﺘﺤﺮك ﻋﺮض ﺑﺮگ ،ﺗﻌﺪاد ﺑﺮگ ،ارﺗﻔﺎع ﺑﻮﺗﻪ و ﺻﻔﺎت ﺷﻴﻤﻴﺎﻳﻲ ﺷﺎﻣﻞ
آب ﺑﺎ درﺟﻪ -HPLCاﺳﺘﻮﻧﻴﺘﺮﻳﻞ ﺑﺎ درﺟﻪ (80/20) HPLC ﻓﻨﻞ و رﺑﺎدﻳﻮزﻳﺪ Aاﻧﺪازهﮔﻴﺮي ﺷﺪ.
ﻣﻲﺑﺎﺷﺪ )ﺷﻜﻞ ﺷﻤﺎره .(1
ﺗﻌﻴﻴﻦ ﻓﻨﻞ ﻛﻞ ﺑﻪ روش ﻓﻮﻟﻴﻦ ﺳﻴﻮ -ﻛﺎﻟﺘﻴﻮ ﺷﺎﺧﺺ ﺳﺒﺰﻳﻨﮕﻲ ﺑﺮگ )(SDAD
)(Folin-Ciocalteau ﺳﺒﺰﻳﻨﮕﻲ ﺑﺮگﻫﺎ ﺑﺎ اﺳﺘﻔﺎده از دﺳﺘﮕﺎه SPADﻣﺪل
ﺑﻪ ﻣﻨﻈﻮر اﻧﺪازهﮔﻴﺮي ﻓﻨﻞ ﺗﺎم 0/1ﮔﺮم از ﺑﺎﻓﺖ ﺑﺮگ ﺧﺸﻚ KONICA MINOLTA-502ﭘﺲ از اﻋﻤﺎل ﺗﻴﻤﺎرﻫﺎ
از ﻳﻚ ﺳﺎﻋﺖ ﺗﺎرﻳﻜﻲ در دﻣﺎي اﺗﺎق ﺗﻮﺳﻂ دﺳﺘﮕﺎه ﺷﺪه ﮔﻴﺎه در ﻫﺎون ﭼﻴﻨﻲ ﺳﺎﻳﻴﺪه و ﭘﺲ از اﺿﺎﻓﻪ ﻛﺮدن 20
اﺳﭙﻜﺘﺮوﻓﺘﻮﻣﺘﺮي (RAYLEIGH) UV-2601در ﻃﻮل ﻣﻮج ﺳﻲﺳﻲ اﺗﺎﻧﻮل 80درﺻﺪ ﺑﻪ ﻣﺪت 48ﺳﺎﻋﺖ روي ﺷﻴﻜﺮ ﻗﺮار
760ﻧﺎﻧﻮﻣﺘﺮ اﻧﺪازهﮔﻴﺮي ﺷﺪ .ﻣﻘﺎدﻳﺮ ﻓﻨﻞ ﺗﺎم ﻋﺼﺎرهﻫﺎ ﺑﺎ اﺳﺘﻔﺎده ﮔﺮﻓﺖ .ﺳﭙﺲ ﻋﺼﺎره ﺗﻮﺳﻂ ﻛﺎﻏﺬ ﺻﺎﻓﻲ واﺗﻤﻦ ﺷﻤﺎره ﻳﻚ،
از ﻣﻨﺤﻨﻲ اﺳﺘﺎﻧﺪارد ﺑﺮ اﺳﺎس ﻣﻴﻠﻲﮔﺮم ﮔﺎﻟﻴﻚ در ﮔﺮم ﻋﺼﺎره ﺻﺎف ﺷﺪ 0/5 .ﺳﻲﺳﻲ ﻋﺼﺎره ﺑﻪ ﻫﻤﺮاه 0/5ﺳﻲﺳﻲ واﻛﻨﺶﮔﺮ
اﻧﺪازهﮔﻴﺮي ﺷﺪ ].[19 0/2ﻧﺮﻣﺎل ﻓﻮﻟﻴﻦ ﺳﻲ و ﻛﺎﻟﺘﻴﻮ و 2/5ﺳﻲﺳﻲ ﺳﺪﻳﻢ ﻛﺮﺑﻨﺎت 20
درﺻﺪ ﺑﺎ ﻏﻠﻈﺖ 75ﮔﺮم در ﻟﻴﺘﺮ ﺑﺎ ﻫﻢ ﺗﺮﻛﻴﺐ ﺷﺪ .ﻧﻤﻮﻧﻪﻫﺎ ﭘﺲ
ﺷﻜﻞ ﺷﻤﺎره -1ﻛﺮوﻣﺎﺗﻮﮔﺮام ﮔﻠﻴﻜﻮزﻳﺪ رﺑﺎدﻳﻮزﻳﺪ ﺗﺤﺖ ﺗﻴﻤﺎرﻫﺎي ﻣﺤﻠﻮلﭘﺎﺷﻲ ﻛﻴﺘﻮزان در ﮔﻴﺎه اﺳﺘﻮﻳﺎ .ﺷﻜﻞ ) :(aاﺳﺘﺎﻧﺪارد رﺑﺎدﻳﻮزﻳﺪ .Aﺷﻜﻞ ):(b
ﻣﺤﻠﻮلﭘﺎﺷﻲ ﻛﻴﺘﻮزان در ﻏﻠﻈﺖ ﺻﻔﺮ .ﺷﻜﻞ ) :(cﻣﺤﻠﻮلﭘﺎﺷﻲ ﻛﻴﺘﻮزان در ﻏﻠﻈﺖ 0/05درﺻﺪ .ﺷﻜﻞ ) :(dﻣﺤﻠﻮلﭘﺎﺷﻲ ﻛﻴﺘﻮزان در ﻏﻠﻈﺖ 0/1درﺻﺪ و
ﺷﻜﻞ ) :(eﻣﺤﻠﻮلﭘﺎﺷﻲ ﻛﻴﺘﻮزان در ﻏﻠﻈﺖ 0/2درﺻﺪ
172
ﻣﻬﺮﮔﺎن و ﻫﻤﻜﺎران
ﺧﺸﻚ ﺳﺎﻗﻪ ﻣﻌﻨﻲدار ﻧﺒﻮد )ﺟﺪول ﺷﻤﺎره .(1در اﻳﻦ ﭘﮋوﻫﺶ ﻧﺘﺎﻳﺞ
ﺑﺮ اﺳﺎس ﻣﻘﺎﻳﺴﻪ ﻣﻴﺎﻧﮕﻴﻦ دادهﻫﺎ ﻣﺤﻠﻮلﭘﺎﺷﻲ ﻛﻴﺘﻮزان در ﺳﻄﺢ ﺗﺄﺛﻴﺮ ﻛﻴﺘﻮزان ﺑﺮ ﺻﻔﺎت ﻣﻮرﻓﻮﻓﻴﺰﻳﻮﻟﻮژﻳﻜﻲ
0/1درﺻﺪ ﺑﻴﺸﺘﺮﻳﻦ وزن ﺧﺸﻚ ﺑﺮگ و اﻧﺪام ﻫﻮاﻳﻲ را ﺗﻮﻟﻴﺪ ﺑﺮ اﺳﺎس ﻧﺘﺎﻳﺞ ﺑﻪ دﺳﺖ آﻣﺪه از ﺗﺠﺰﻳﻪ وارﻳﺎﻧﺲ دادهﻫﺎ
ﻧﻤﻮد ،ﺑﻪ ﻃﻮري ﻛﻪ ﺑﺎ اﻓﺰاﻳﺶ ﻏﻠﻈﺖ ﻛﻴﺘﻮزان از 0/1ﺑﻪ 0/2 ﻣﺤﻠﻮلﭘﺎﺷﻲ ﻣﺤﺮك زﻳﺴﺘﻲ ﻛﻴﺘﻮزان ﺑﺮ وزن ﺧﺸﻚ ﺑﺮگ ،وزن
درﺻﺪ اﻳﻦ ﺻﻔﺎت ﻛﺎﻫﺶ ﻳﺎﻓﺖ )ﺷﻜﻞ ﺷﻤﺎرهﻫﺎي 2و .(3 ﺧﺸﻚ اﻧﺪام ﻫﻮاﻳﻲ ) (P<0/05اﺛﺮ ﻣﻌﻨﻲداري داﺷﺘﻪ )ﺟﺪول
ﺷﻤﺎره (1و ﺑﺮ ﺻﻔﺎت وزن ﺗﺮ ﺑﺮگ و اﻧﺪام ﻫﻮاﻳﻲ و وزن ﺗﺮ و
174
ﻣﻬﺮﮔﺎن و ﻫﻤﻜﺎران
ﻣﻘﺎﻳﺴﻪ ﻣﻴﺎﻧﮕﻴﻦ دادهﻫﺎ ﺑﻴﺸﺘﺮﻳﻦ ﻣﻴﺰان ﻓﻨﻞ در ﻏﻠﻈﺖ 0/1 ﺑﺮ اﺳﺎس ﻧﺘﺎﻳﺞ ﺑﻪ دﺳﺖ آﻣﺪه از ﺗﺠﺰﻳﻪ وارﻳﺎﻧﺲ دادهﻫﺎي
درﺻﺪ ﻛﻴﺘﻮزان ﻣﺸﺎﻫﺪه ﺷﺪ )ﺷﻜﻞ ﺷﻤﺎره .(5 ﻣﺤﻠﻮلﭘﺎﺷﻲ ﻣﺤﺮك زﻳﺴﺘﻲ ﻛﻴﺘﻮزان ﺑﺮ ﻃﻮل ﺑﺮگ )(P<0/05
اﺛﺮ ﻣﻌﻨﻲداري داﺷﺘﻪ و ﺑﺮ ﺻﻔﺎت ﻋﺮض ﺑﺮگ ،وزن ﺗﺮ و ﺧﺸﻚ
ﺗﺄﺛﻴﺮ ﻛﻴﺘﻮزان ﺑﺮ رﺑﺎدﻳﻮزﻳﺪ A رﻳﺸﻪ ﻣﻌﻨﻲدار ﻧﺒﻮد )ﺟﺪول ﺷﻤﺎره (1و در اﻳﻦ آزﻣﺎﻳﺶ ﺑﺮ
در اﻳﻦ ﭘﮋوﻫﺶ ﻧﺘﺎﻳﺞ ﺑﻪ دﺳﺖ آﻣﺪه از ﺗﺠﺰﻳﻪ وارﻳﺎﻧﺲ اﺳﺎس ﻣﻘﺎﻳﺴﻪ ﻣﻴﻨﮕﻴﻦ دادهﻫﺎ ،ﺗﻴﻤﺎر ﺷﺎﻫﺪ ﺑﻴﺸﺘﺮﻳﻦ ﺗﺄﺛﻴﺮ را ﺑﺮ
دادهﻫﺎ ﻧﺸﺎن داد ﻛﻪ ﻣﺤﻠﻮلﭘﺎﺷﻲ ﻛﻴﺘﻮزان اﺛﺮ ﻣﻌﻨﻲداري ﺑﺮ ﻃﻮل ﺑﺮگ داﺷﺘﻪ اﺳﺖ )ﺷﻜﻞ ﺷﻤﺎره .(4
رﺑﺎدﻳﻮزﻳﺪ (P<0/01) Aداﺷﺘﻪ اﺳﺖ )ﺟﺪول ﺷﻤﺎره (2ﺑﻪ
ﻃﻮري ﻛﻪ ﺑﺮ اﺳﺎس ﻣﻘﺎﻳﺴﻪ ﻣﻴﺎﻧﮕﻴﻦ دادهﻫﺎي آزﻣﺎﻳﺶ ﺗﺄﺛﻴﺮ ﻛﻴﺘﻮزان ﺑﺮ ﻓﻨﻞ
ﻣﺤﻠﻮلﭘﺎﺷﻲ ﻛﻴﺘﻮزان ﺑﺎ ﻏﻠﻈﺖ 0/2درﺻﺪ ﺑﻴﺸﺘﺮﻳﻦ ﺗﺄﺛﻴﺮ را در اﻳﻦ ﭘﮋوﻫﺶ ﻧﺘﺎﻳﺞ ﺑﻪ دﺳﺖ آﻣﺪه از ﺗﺠﺰﻳﻪ وارﻳﺎﻧﺲ
ﺑﺮ رﺑﺎدﻳﻮزﻳﺪ Aداﺷﺘﻪ اﺳﺖ )ﺷﻜﻞ ﺷﻤﺎره .(6 دادهﻫﺎ ﻧﺸﺎن ﻣﻲدﻫﺪ ﻛﻪ ﻣﺤﻠﻮلﭘﺎﺷﻲ ﻛﻴﺘﻮزان اﺛﺮ ﻣﻌﻨﻲداري ﺑﺮ
ﻓﻨﻞ ) (P<0/01داﺷﺘﻪ اﺳﺖ )ﺟﺪول ﺷﻤﺎره (2و ﺑﺮ اﺳﺎس
ﺟﺪول ﺷﻤﺎره -2ﺗﺠﺰﻳﻪ وارﻳﺎﻧﺲ اﺛﺮ ﻣﺤﺮك زﻳﺴﺘﻲ ﻛﻴﺘﻮزان ﺑﺮ ﺻﻔﺎت ﺑﻴﻮﺷﻴﻤﻴﺎﻳﻲ ﮔﻴﺎه داروﻳﻲ اﺳﺘﻮﻳﺎ
ﻓﻨﻮل رﺑﺎدﻳﻮزﻳﺪ A درﺟﻪ آزادي ﻣﻨﺎﺑﻊ ﺗﻐﻴﻴﺮ
0/004 ns 0/12 ns 2 ﺑﻠﻮك
**0/18 **8/47 3 ﻛﻴﺘﻮزان
0/015 0/7 6 ﺧﻄﺎ
7/65 12/75 - ﺿﺮﻳﺐ ﺗﻐﻴﻴﺮات )درﺻﺪ(
⃰ ⃰ ﻣﻌﻨﻲدار در ﺳﻄﺢ اﺣﺘﻤﺎل 1درﺻﺪ ⃰ .ﻣﻌﻨﻲدار ﺳﻄﺢ اﺣﺘﻤﺎل 5درﺻﺪ ns .ﻣﻌﻨﻲدار ﻧﻤﻲﺑﺎﺷﺪ
ﺧﺸﻚ ﺑﺮگ و اﻧﺪام ﻫﻮاﻳﻲ در ﮔﻴﺎه ﻓﻠﻔﻞ دﻟﻤﻪاي ﺷﺪه اﺳﺖ ﺑﺤﺚ
] .[27ﺑﻪ ﺗﺎزﮔﻲ ﮔﺰارش ﺷﺪه اﺳﺖ ﻛﻪ ﻛﻴﺘﻮزان ﺑﺎﻋﺚ رﺷﺪ، ﺗﺄﺛﻴﺮ ﻛﻴﺘﻮزان ﺑﺮ ﺻﻔﺎت ﻣﻮرﻓﻮﻓﻴﺰﻳﻮﻟﻮژﻳﻜﻲ
ﺗﻮﺳﻌﻪ ﺳﻠﻮﻟﻲ و در ﻧﺘﻴﺠﻪ اﻓﺰاﻳﺶ ﻋﻤﻠﻜﺮد در ﮔﻴﺎه ﻣﻲﺷﻮد، ﻣﺤﻠﻮلﭘﺎﺷﻲ ﻛﻴﺘﻮزان ﺑﺎﻋﺚ اﻓﺰاﻳﺶ رﺷﺪ روﻳﺸﻲ در ﮔﻴﺎه
ﻛﻴﺘﻮزان ﺑﺎ اﺳﺘﻔﺎده از اﻓﺰاﻳﺶ ﻓﻌﺎﻟﻴﺖ آﻧﺰﻳﻢﻫﺎي ﻛﻠﻴﺪي در ﻛﻠﻢ ] ،[20ذرت ] ،[21ﻟﻮﺑﻴﺎ ] [22و اﻓﺰاﻳﺶ وزن ﺧﺸﻚ اﻧﺪام
ﻣﺘﺎﺑﻮﻟﻴﺴﻢ ﻧﻴﺘﺮوژن )ﻧﻴﺘﺮاتردﻛﺘﺎز ،ﮔﻠﻮﺗﺎﻣﻴﻦ و ﭘﺮوﺗﺌﺎزﺳﻨﺘﺘﺎز( و ﻫﻮاﻳﻲ در ﮔﻴﺎه ﮔﻠﺮﻧﮓ ﺷﺪ [23] ،ﺷﺪه اﺳﺖ .ﻛﺎرﺑﺮد ﺑﺮﮔﻲ
ﺑﻬﺒﻮد اﻧﺘﻘﺎل ﻧﻴﺘﺮوژن ﺑﺎﻋﺚ ﺗﻮﺳﻌﻪ و رﺷﺪ ﻣﻲﺷﻮد ] .[28ﻃﺒﻖ ﻛﻴﺘﻮزان ﺑﺮ رﺷﺪ و وﻳﮋﮔﻲﻫﺎي ﻣﻮرﻓﻮﻟﻮژﻳﻜﻲ ﮔﻴﺎه داروﻳﻲ
ﻣﺤﺘﻮاي ﻛﻴﺘﻮزان اﺳﭙﺮي ﮔﺮﻓﺘﻪ ﺻﻮرت ﺑﺮرﺳﻲﻫﺎي ﻫﻤﻴﺸﻪﺑﻬﺎر ) (Calendula officinalisﺗﺄﺛﻴﺮ ﮔﺬاﺷﺘﻪ و ﺑﻪ
اﺳﻴﺪآﺑﺴﺰﻳﻚ را در ﺑﺮگﻫﺎ اﻓﺰاﻳﺶ ﻣﻲدﻫﺪ ] ،[29ﻣﺤﻘﻘﻴﻦ در ﻋﻨﻮان ﻋﺎﻣﻞ ﻣﺜﺒﺘﻲ در ﺑﺴﻴﺎري از وﻳﮋﮔﻲﻫﺎي ﻣﻮرﻓﻮﻟﻮژﻳﻜﻲ و
ﭘﮋوﻫﺸﻲ دﻳﮕﺮ درﻳﺎﻓﺘﻨﺪ ﻛﻪ ﻛﺎرﺑﺮد 0/5درﺻﺪ ﻛﻴﺘﻮزان ﺑﺮ روي رﺷﺪ )ارﺗﻔﺎع ﺑﻮﺗﻪ ،وزن ﺗﺮ و ﺧﺸﻚ اﻧﺪامﻫﺎي ﻫﻮاﻳﻲ( ﻣﺆﺛﺮ
رﺷﺪ و ﻋﻤﻠﻜﺮد ﺗﺮﺑﭽﻪ ﺗﺄﺛﻴﺮ ﮔﺬاﺷﺘﻪ و ﺑﺎﻋﺚ اﻓﺰاﻳﺶ ﺳﻄﺢ ﺑﺮگ اﺳﺖ ] ،[24ﻫﻤﭽﻨﻴﻦ در ﭘﮋوﻫﺶ دﻳﮕﺮ ﻛﻪ ﺑﺮ روي ﮔﻴﺎه
و وزن ﺧﺸﻚ ﮔﻴﺎه ﻣﻲﺷﻮد ] ،[30ﻫﻤﭽﻨﻴﻦ ﻣﺤﻠﻮلﭘﺎﺷﻲ ﻛﻴﺘﻮزان ﮔﻮﺟﻪﻓﺮﻧﮕﻲ ﺻﻮرت ﮔﺮﻓﺖ ﻣﺤﻠﻮلﭘﺎﺷﻲ ﻛﻴﺘﻮزان ﺑﺎﻋﺚ اﻓﺰاﻳﺶ
ﻫﺪاﻳﺖ روزﻧﻪاي را اﻓﺰاﻳﺶ ﻣﻲدﻫﺪ و ﺑﺎﻋﺚ ﻛﺎﻫﺶ ﺗﻌﺮق ،ﺑﺪون ﺗﻌﺪاد ﺷﺎﺧﻪ ،ﺗﻌﺪاد ﺑﺮگ ،وزن ﺧﺸﻚ ﺑﺮگ و اﻧﺪام ﻫﻮاﻳﻲ ﺷﺪ
ﺗﺄﺛﻴﺮ در ارﺗﻔﺎع ﺑﻮﺗﻪ ،ﻃﻮل رﻳﺸﻪ ،ﺳﻄﺢ ﺑﺮگ و ﻳﺎ زﻳﺴﺖﺗﻮده ] [25و در ﺗﺤﻘﻴﻘﺎت ﻣﺸﺎﺑﻪ ﻛﻪ ﺑﺮ روي ﮔﻴﺎه ﺗﻮتﻓﺮﻧﮕﻲ و ﺑﺮﻧﺞ
ﮔﻴﺎﻫﻲ ﻣﻲﺷﻮد ] .[17ﺗﺎ ﺑﻪ ﺣﺎل ﺳﺎزوﻛﺎر ﻋﻤﻞ ﻛﻴﺘﻮزان روي اﻧﺠﺎم ﺷﺪه ﺗﻴﻤﺎر ﻛﻴﺘﻮزان ﺑﺎﻋﺚ اﻓﺰاﻳﺶ وزن ﺗﺮ و ﺧﺸﻚ ﺑﺮگ
رﺷﺪ ﻧﺎﺷﻨﺎﺧﺘﻪ ﺑﺎﻗﻲ ﻣﺎﻧﺪه اﺳﺖ .اﺣﺘﻤﺎﻻً ﻛﻴﺘﻮزان ﺳﻴﮕﻨﺎﻟﻲ را ﺷﺪه اﺳﺖ ] .[21-26ﻛﺎرﺑﺮد ﺑﺮﮔﻲ ﻛﻴﺘﻮزان ﺑﺎﻋﺚ اﻓﺰاﻳﺶ وزن
176
ﻣﻬﺮﮔﺎن و ﻫﻤﻜﺎران
داده اﺳﺖ ﻛﻪ ﻛﻴﺘﻮزان ﺑﻪ ﻋﻨﻮان ﻳﻚ اﻟﻴﺴﻴﺘﻮر زﻳﺴﺘﻲ ﻣﻤﻜﻦ اﺳﺖ ﺑﺮاي ﺳﻨﺘﺰ ﻫﻮرﻣﻮنﻫﺎي ﮔﻴﺎﻫﻲ ﻣﺎﻧﻨﺪ ﺟﻴﺒﺮﻟﻴﻦ اﻟﻘﺎء ﻣﻲﻛﻨﺪ و
داراي ﭘﺘﺎﻧﺴﻴﻞ ﺑﺮاي از ﺑﻴﻦ ﺑﺮدن رادﻳﻜﺎلﻫﺎي آزاد ﺑﺎﺷﺪ ].[40 ،41 رﺷﺪ و ﻧﻤﻮ ﮔﻴﺎه را ﺗﻮﺳﻂ ﺑﻌﻀﻲ ﻣﺴﻴﺮﻫﺎي ﺳﻴﮕﻨﺎﻟﻴﻨﮓ ﻣﺮﺑﻮط
ﻛﻪ ﺑﺎﻋﺚ اﻓﺰاﻳﺶ ﻣﻴﺰان ﺗﺮﻛﻴﺒﺎت ﻓﻨﻠﻲ ﻣﻲﺷﻮد ].[42 ﺑﻪ ﺑﻴﻮﺳﻨﺘﺰ اﻛﺴﻴﻦ ،از ﻃﺮﻳﻖ ﻣﺴﻴﺮ واﺑﺴﺘﻪ ﺑﻪ ﺗﺮﻳﭙﺘﻮﻓﺎن ،اﻓﺰاﻳﺶ
دﻫﺪ ] .[24ﻣﺤﻠﻮلﭘﺎﺷﻲ ﻛﻴﺘﻮزان ﺑﺎﻋﺚ اﻓﺰاﻳﺶ ﺳﻄﺢ ﺑﺮگ ﮔﻴﺎه
ﺗﺄﺛﻴﺮ ﻛﻴﺘﻮزان ﺑﺮ رﺑﺎدﻳﻮزﻳﺪ A ﮔﻠﺮﻧﮓ در ﺷﺮاﻳﻂ ﺑﺪون ﺗﻨﺶ ﻧﺴﺒﺖ ﺑﻪ ﺗﻴﻤﺎر ﺷﺎﻫﺪ ﺷﺪ ]،[31
ﻣﻄﺎﻟﻌﺎت ﻣﺘﻌﺪدي ﻧﺸﺎن دادهاﻧﺪ ﻛﻪ ﺗﺮﻛﻴﺒﺎت اﺻﻠﻲ دﻳﻮاره در آزﻣﺎﻳﺶ دﻳﮕﺮ از ﻣﺤﻠﻮلﭘﺎﺷﻲ ﻛﻴﺘﻮزان در ﮔﻴﺎه ﻟﻮﺑﻴﺎ ﻧﺘﺎﻳﺞ
ﺳﻠﻮﻟﻲ ﺑﺴﻴﺎري از ﮔﻮﻧﻪﻫﺎي ﻗﺎرﭼﻲ ﻣﺎﻧﻨﺪ ﻛﺘﻴﻦ و ﻛﻴﺘﻮزان ،ﺑﺎﻋﺚ ﻣﺸﺎﺑﻪ ﺣﺎﺻﻞ ﮔﺮدﻳﺪ ] .[21ﻛﻴﺘﻮزان در اﻓﺰاﻳﺶ ﻛﻠﺮوﻓﻴﻞ و
ﺗﻮﻟﻴﺪ ﻣﺘﺎﺑﻮﻟﻴﺖﻫﺎي ﺛﺎﻧﻮﻳﻪ ] [43و ﺗﺤﺮﻳﻚ ﻣﻜﺎﻧﻴﺴﻢﻫﺎي دﻓﺎﻋﻲ ﻓﺘﻮﺳﻨﺘﺰ ﻧﻘﺶ دارد و ﻋﻼوه ﺑﺮ اﻳﻦ ،ﻛﻴﺘﻮزان ﺑﻴﺎن ژن
ﮔﻴﺎه ﻣﻲﺷﻮد ] .[44ﻛﻴﺘﻮزان ﺑﻪ ﻋﻨﻮان ﻳﻚ آﻣﻴﻨﻮ ﭘﻠﻲﺳﺎﻛﺎرﻳﺪ ﻛﻠﺮوﭘﻼﺳﺖ ﺑﺮگ را ﺗﺤﺖ ﺗﺄﺛﻴﺮ ﻗﺮار ﻣﻲدﻫﺪ ﺑﻪ ﻃﻮري ﻛﻪ ﺗﻐﻴﻴﺮ
ﻃﺒﻴﻌﻲ ﺑﺎ ﺳﺎﺧﺘﺎري ﺑﻲﻧﻈﻴﺮ و ﺳﻤﻴﺖ ﭘﺎﻳﻴﻦ ] [45ﺑﺎﻋﺚ ﺑﻴﺎن در اﻧﺪازه ﻛﻠﺮوﭘﻼﺳﺖ ﻣﻤﻜﻦ اﺳﺖ ﻋﺎﻣﻞ ﺗﺤﺮﻳﻚ ﻛﻨﻨﺪه رﺷﺪ
اﻧﻮاع ژنﻫﺎي دﺧﻴﻞ در ﭘﺎﺳﺦ دﻓﺎﻋﻲ ﮔﻴﺎه در ﺷﺮاﻳﻂ ﺗﻨﺶ ﺷﺪه ﮔﻴﺎﻫﺎن ﺑﺎﺷﺪ ] ،[32ﻫﻤﭽﻨﻴﻦ در ﺷﺮاﻳﻂ ﺗﻨﺶ ﻛﻴﺘﻮزان از ﻃﺮﻳﻖ
ﻛﻪ ﻣﻨﺠﺮ ﺑﻪ اﻓﺰاﻳﺶ ﺗﻮﻟﻴﺪ ﻣﺘﺎﺑﻮﻟﻴﺖﻫﺎي ﺛﺎﻧﻮﻳﻪ ﮔﻴﺎﻫﻲ ﻣﻲﺷﻮد اﻓﺰاﻳﺶ ﻣﺤﺘﻮاي ﻧﺴﺒﻲ آب ﺑﺮگ ،ﻣﻨﺠﺮ ﺑﻪ ﺣﻔﻆ ﺗﻮرژﺳﺎﻧﺲ و
] .[46ﻫﻤﭽﻨﻴﻦ درﺧﺼﻮص اﻟﻴﺴﻴﺘﻮر ﻛﻴﺘﻮزان ﻣﻲﺗﻮان ﮔﻔﺖ ﻛﻪ ﺣﺠﻢ ﺑﺮك ﻣﻲﺷﻮد و از ﻏﺸﺎي ﺳﻠﻮﻟﻲ را ﻣﺤﺎﻓﻈﺖ ﻣﻲﻛﻨﺪ
اﻟﻴﺴﻴﺘﻮرﻫﺎ ﻣﻤﻜﻦ اﺳﺖ ،ژنﻫﺎي ﺟﺪﻳﺪي را ﻓﻌﺎل ﻛﻨﻨﺪ ﻛﻪ ] .[33ﺑﺮ اﺳﺎس ﻧﺘﺎﻳﺞ ﺑﻪ دﺳﺖ آﻣﺪه از ﺗﺠﺰﻳﻪ وارﻳﺎﻧﺲ دادهﻫﺎي
آﻧﺰﻳﻢﻫﺎ و در ﻧﻬﺎﻳﺖ ﻣﺴﻴﺮﻫﺎي ﺑﻴﻮﺳﻨﺘﺰي ﻣﺨﺘﻠﻔﻲ را راهاﻧﺪازي آزﻣﺎﻳﺶ ﻣﺤﻠﻮلﭘﺎﺷﻲ ﻣﺤﺮك زﻳﺴﺘﻲ ﻛﻴﺘﻮزان ﺑﺮ ﺻﻔﺎت ارﺗﻔﺎع
ﻣﻲﻛﻨﻨﺪ و ﺑﺎﻋﺚ ﺗﺸﻜﻴﻞ ﻣﺘﺎﺑﻮﻟﻴﺖﻫﺎي ﺛﺎﻧﻮﻳﻪ ﻣﻲﺷﻮﻧﺪ ] ،[47در ﺑﻮﺗﻪ ،ﺗﻌﺪاد ﺑﺮگ و ﺷﺎﺧﺺ ﺳﺒﺰﻳﻨﮕﻲ ﺑﺮگ ) (SPADاﺛﺮ
ﺗﺤﻘﻴﻘﺎﺗﻲ ﻛﻪ ﺑﺮ روي ﮔﻴﺎه زﻧﻴﺎن و ﮔﻠﺮﻧﮓ اﻧﺠﺎم ﺷﺪ ﻣﻴﺰان ﻣﻌﻨﻲداري ﻧﺪاﺷﺖ )ﺟﺪول ﺷﻤﺎره .(1
ﻗﻨﺪﻫﺎي ﻣﺤﻠﻮل ﺗﺤﺖ ﺗﺄﺛﻴﺮ ﺗﻴﻤﺎر ﻛﻴﺘﻮزان ﻗﺮار ﮔﺮﻓﺖ ]،49
،[48ﻫﻤﭽﻨﻴﻦ در ﭘﮋوﻫﺸﻲ ﻛﻪ ﺑﺮ روي ﮔﻴﺎه ﺑﺎدرﻧﺠﺒﻮﻳﻪ ﺻﻮرت ﺗﺄﺛﻴﺮ ﻛﻴﺘﻮزان ﺑﺮ ﻓﻨﻞ
ﮔﺮﻓﺖ ﺑﺎ اﻓﺰاﻳﺶ ﻏﻠﻈﺖ ﻛﻴﺘﻮزان ﻣﻴﺰان ﻛﺮﺑﻮﻫﻴﺪرات اﻓﺰاﻳﺶ ﻧﻘﺶ ﺗﺮﻛﻴﺒﺎت ﻓﻨﻠﻲ ﻣﺮﺑﻮط ﺑﻪ ﺧﻮاص اﻛﺴﻴﺪاﺳﻴﻮن اﺣﻴﺎء
ﻳﺎﻓﺖ ] [50و در ﺑﺮرﺳﻲ دﻳﮕﺮي ﻛﻪ ﺑﺮ روي ﮔﻴﺎه رﻳﺤﺎن اﻧﺠﺎم آﻧﻬﺎ اﺳﺖ ﻛﻪ ﻧﻘﺶ ﻣﻬﻤﻲ در ﺟﺬب و ﺧﻨﺜﻲﺳﺎزي رادﻳﻜﺎلﻫﺎي
ﺷﺪ ﻛﻴﺘﻮزان از ﻃﺮﻳﻖ اﻟﻘﺎي ﺳﻴﺴﺘﻢ دﻓﺎﻋﻲ ﺑﺎﻋﺚ ﺑﻬﺒﻮد ﺑﺨﺸﻴﺪن آزاد ،ﻓﺮوﻧﺸﺎﻧﻲ اﻛﺴﻴﮋنﻫﺎي ﻓﻌﺎل و ﻳﺎ ﭘﺮاﻛﺴﻴﺪازﻫﺎي ﺗﺠﺰﻳﻪ
ﺑﻪ ﺑﻴﻮﺳﻨﺘﺰ ﻣﺘﺎﺑﻮﻟﻴﺖﻫﺎي ﺛﺎﻧﻮﻳﻪ ،اﻓﺰاﻳﺶ ﻛﺮﺑﻮﻫﻴﺪرات در رﻳﺸﻪ ﻛﻨﻨﺪه دارﻧﺪ ] .[34اﻧﺒﺎﺷﺘﮕﻲ اﻧﻮاع ﺗﺮﻛﻴﺒﺎت ﻓﻨﻠﻲ در ﺷﺮاﻳﻂ
و اﻓﺰاﻳﺶ رﺷﺪ ﺷﺪه اﺳﺖ ] .[51در واﻗﻊ ﺑﺎ اﻓﺰاﻳﺶ ﻏﻠﻈﺖ ﺗﻨﺸﻲ ﻣﻲﺗﻮاﻧﺪ ﺑﻪ ﻋﻨﻮان ﻳﻚ ﻋﻼﻣﺖ ﻋﻤﻞ ﻛﻨﺪ و ﺑﺮاي
ﻛﻴﺘﻮزان ،ﺗﻐﻴﻴﺮات ﻓﺮاﺳﺎﺧﺘﺎري در اﻧﺪاﻣﻚﻫﺎي ﺳﻠﻮﻟﻲ از ﻗﺒﻴﻞ راهاﻧﺪازي زﻧﺠﻴﺮﻫﺎي از واﻛﻨﺶﻫﺎي دﻳﮕﺮ ﻛﻪ در ﻧﻬﺎﻳﺖ ﺑﻪ
ﺗﻮﻧﻮﭘﻼﺳﺖ و آﻧﺰﻳﻢﻫﺎي ﻣﺴﻴﺮ ﻣﺘﺎﺑﻮﻟﻴﺴﻢ ﻗﻨﺪﻫﺎ اﻳﺠﺎد ﻣﻲﺷﻮد، اﻓﺰاﻳﺶ ﺗﺤﻤﻞ ﺗﻨﺶ ﻣﻨﺠﺮ ﻣﻲﺷﻮﻧﺪ ،ﻋﻤﻞ ﻧﻤﺎﻳﺪ ] .[35در
ﻛﻪ اﻳﻦ ﻧﻮع ﻣﻜﺎﻧﻴﺴﻢ ﺗﻄﺎﺑﻘﻲ و ﺳﺎزﮔﺎر ﻳﺎﻓﺘﻪ ﺑﺮاي ﺣﻔﻆ و ﭘﮋوﻫﺸﻲ ﻛﻪ ﺑﺮ روي ﮔﻴﺎه زﻧﻴﺎن اﻧﺠﺎم ﺷﺪ ﻣﺤﻠﻮل ﭘﺎﺷﻲ ﻛﻴﺘﻮزان
ﻧﮕﻬﺪاري ﭘﺘﺎﻧﺴﻴﻞ اﺳﻤﺰي ﺗﺤﺖ ﺗﻴﻤﺎر ﻛﻴﺘﻮزان ﻣﻲﺑﺎﺷﺪ و ) (200 ppmﻣﻴﺰان ﺗﺮﻛﻴﺒﺎت ﻓﻨﻠﻲ را ﻧﺴﺒﺖ ﺑﻪ ﺷﺎﻫﺪ اﻓﺰاﻳﺶ داد
اﻓﺰاﻳﺶ ﻣﺤﺘﻮاي ﻗﻨﺪ ،ﺗﺤﺖ ﺗﻴﻤﺎر ﻣﺤﻠﻮلﭘﺎﺷﻲ ﻛﻴﺘﻮزان ﻣﺸﺎﻫﺪه ] [36و ﻃﺒﻖ ﺗﺤﻘﻴﻘﺎت اﻧﺠﺎم ﺷﺪه ﺗﻴﻤﺎر ﻛﻴﺘﻮزان ﺑﺎﻋﺚ اﻓﺰاﻳﺶ
ﻣﻲﺷﻮد ﻛﻪ اﺣﺘﻤﺎﻻً ﺑﻪ دﻟﻴﻞ ﻫﻴﺪروﻟﻴﺰ ﻧﺸﺎﺳﻪ و اﻓﺰاﻳﺶ ﻗﻨﺪﻫﺎي ﻓﻌﺎﻟﻴﺖ ﺗﺮﻛﻴﺒﺎت ﻓﻨﻠﻲ در ﮔﻴﺎه ﮔﻮﺟﻪﻓﺮﻧﮕﻲ ﻣﻲﺷﻮد ] .[37در
ﻣﺤﻠﻮل ﺣﺎﺻﻞ از آن اﺳﺖ ] ،[52ﺑﺮ اﺳﺎس ﻧﺘﺎﻳﺞ ﺑﻪ دﺳﺖ آﻣﺪه ﭘﮋوﻫﺸﻲ دﻳﮕﺮ ﻣﺸﺨﺺ ﺷﺪ ﻛﻪ ﻛﺎرﺑﺮد ﺑﺮﮔﻲ ﻛﻴﺘﻮزان در ﮔﻴﺎه ﭼﺎي
اﻳﻦ آزﻣﺎﻳﺶ ﻧﻴﺰ ﻣﺤﻠﻮلﭘﺎﺷﻲ ﻛﻴﺘﻮزان ﺑﺎﻋﺚ اﻓﺰاﻳﺶ و ﻛﺘﺎن ﺳﻔﻴﺪ ﺳﺒﺐ اﻓﺰاﻳﺶ ﻗﺎﺑﻞ ﺗﻮﺟﻬﻲ در ﻣﺤﺘﻮاي ﻓﻨﻠﻲ ﺑﺮگﻫﺎ
ﻣﺘﺎﺑﻮﻟﻴﺖﻫﺎي ﺛﺎﻧﻮﻳﻪ در ﮔﻴﺎه اﺳﺘﻮﻳﺎ ﺷﺪه اﺳﺖ. ﻧﺴﺒﺖ ﺑﻪ ﺗﻴﻤﺎر ﺷﺎﻫﺪ ﺷﺪه اﺳﺖ ] .[38 ،39ﻣﻄﺎﻟﻌﺎت اﺧﻴﺮ ﻧﺸﺎن
ﻣﻨﺎﺑﻊ
1. David J Midmore. A new rural industry-Stevia- 9. Cheng X, Zhou U and Cui X. Improvement of
to replace imported chemical sweeteners. In: Rural phenylethanoid glycosides biosynthesis in
Industries Research and Development Corporation. Cistanche deserticola cell suspension cultures by
RIRDC Web Publication No W02/022. 2002. chitosan elicitor. Biotechnol. J. 121: 253 - 60.
2. Soejarto D. Botany of Stevia and Stevia 10. Pariser ER and Lombardi DP. A guide to the
rebaudiana. In A. Kinghorn (Ed.), Stevia: The research literature chitin, Source book. Plenum
genus Stevia. London, New York: Taylor and Press. New York, U.S.A. 1988, p: 560.
Francis. 2002, pp: 18-39. 11. Pichynagkura R and Kudan S. Quantitative
3. Buana L and Goenadi DH. A study on the production of 2-acetamido 2-deoxy-Dglucose from
correlation between growth and yield in Stevia. Cryatallin Chitin by Bactrial Chitinase.
Menara Perkebunan 1985; 53 (3): 68-71. Carbohydrate Res. 2002; 337: 1-9.
4. Gregersen S, Jeppesen PB, Holst JJ and 12. Arriola OC, Rocha MC, Hernandez AB,
Hermansen K. Antihyperglycemic effects of Brauer JME and Jatomea MP. Controlled release
stevioside in type 2 diabetic subjects. Metabolism matrices and micro/nanoparticles of chitosan with
Clinical and Experimental 2004; 53: 73 - 6. antimicrobial potential: development of new
5. Starratt AN, Kirby CW, Pocs R and Brandle JE. strategies for microbial control in agriculture.
Rebaudioside F, a diterpene glycoside from Stevia Journal of the Science of Food and Agriculture
rebaudiana. Phytochem. 2002; 59: 367 - 70. 2013; 93 (7): 1525 - 36.
6. Goyal SK and Goyal RK. Stevia (Stevia 13. Rabea EI, Badawy ME, Stevens CV, Smagghe
rebaudiana) a bio-sweetener: a review. Int. J. Food G and Steurbaut W. Chitosan as antimicrobial
Sci. Nutr. 2010; 61: 1-10. agent: Aplications and mode of action.
7. Adari Bhaskar Rao, Ernala Prasad, Goka Roopa Biomacromolecules 2003; 4 (5): 1457 - 65.
and Sundergopal Sridhar. Simple extraction and 14. Agrawal G, Rakwal R, Tamogami S,
membrane purification process in isolation of Yonekurad M, Kubo A and Saji H. Chitosan
steviosides with improved organoleptic activity. activates defense/stress response(s) in the leaves f
Advances in Bioscience and Biotechnol. 2012; 3: Oryza Sativa seedlings. Plant Physiology and
327-35. Biochem. 2002; 40: 1061-9.
8. Zhao J, Davis LC and Verpoorte R. Elicitor 15. Harish Prashanth KV, Dharmesh SM,
signal transduction leading to production of plant Jagannatha Rao KS and Tharanathan RN. Free
secondary metabolites. Biotechnol. Adv. 2005; 23 radical-induced chitosan depolymerized products
(4): 283–333
178
ﻣﻬﺮﮔﺎن و ﻫﻤﻜﺎران
protect calf thymus DNA from oxidative damage. Conference of passive defense in the agricultural
Carbohydrate Res. 2007; 342: 190 - 5. sector. 2013 November 30.
16. Luan L.Q., Ha. V.T.T., Nagasawa N, Kume T, 25. El-Tantawy E.M. Behavior of tomato plants as
Yoshii F and Nakanishi T.M. Biological effect of affected by spraying with chitosan and aminofort
irradiated chitosan on plantsin vitro, Biotechnology as natural stimulator substances under application
and Applied Biochemistry 2005; 41: 49 - 57. of soil organic amendments. Pakistan J. Biol. Sci.
17. No HK, Young PN, Ho LS and Meyers SP. 2009; 12 (17): 1164 - 73.
Antibacterial activity of chitosans and chitosan 26. Abdel-Mawgoud AMR, Tantawy AS, El-Nemr
oligomers with different molecular weights. Int. MA and Sassine YN. Growth and yield responses
Food Microbiol. 2002; 74: 65-72 of strawberry plants to chitosan application.
18. Jiang Y and Li Y. Effects of chitosan coating European Journal of Scientific Res. 2010; 39 (1):
on postharvest life and quality of longan fruit. 161-8.
Food Chemistry 2001; 73: 139 - 43. 27. Ghoname A.A, M. A. El-Nemr, A. M. R
19. Wettasinghe M and Shahid F. Antioxidant and Abdel-Mawgoud and W. A. El-Tohamy.
free radical-scavenging properties of ethanolic Enhancement of Sweet Pepper crop growth and
extracts of defatted borage (Borago officinalis L.) production by application of biological, organic
seeds. Food Chem. 1999; 67: 399 - 414. and nutritional solutions. Research J. Agric. Bio.
20. Hirano S. The activation of plant cells and their Sci. 2010; 6 (3): 349 - 355.
self-defence function against pathogens in 28. Mondal MA, Malek MA, Puteh AB, Ismail
connection with Chitosan. Nippon Nogeikagaku MR, Ashrafuzzaman M and Naher L. Effect of
Kaishi 1988; 62: 293-295 (in Japanese with foliar application of chitosan on growth and yield
English summery). in okra. Australian Journal of Crop Science. 2012;
21. Sheikha SAAK and AL-Malki FM. Growth 6(5): 918-921
and chlorophyll responses of bean plants to the 29. Qin CH, Xiao Q, Liu Y, Zhu J and Du Y.
chitosan applications. Eur. J. Sci. Res. 2011; 50: Water-Solubility of chitosan and its antimicrobial
124 - 34. activity. Carbohydrate Polymers 2006; 63: 367-74.
22. Guan Y.J., J. Hu, X.J. Wang and C.X. Shao. 30. Chibu H, Shibayama H and Susuma A. Effects
Seed priming with chitosan improves maize of Chitosan Application on the Shoot Growth of
germination and seedling growth in relation to Rice and Soybean. Japanese Journal of Crop
physiological changes under low temperature Science. 2001; 71 (2): 206 - 11.
stress. J. Zhejiang Univ. Sci. 2009; 10 (6): 427 - 31. Mahdavi B, ModarresSanavy S.A.M.,
33. Aghaalikhani M and Sharifi M. Effect of water
23. Mahdavi B, Modares Sani AM, AghaAlikhani stress and chitosan on Germination and proline of
M and Sharifi M. The effect of chitosan and water seedling in safflower (Carthamus tinctorius L.).
stress on morphological characteristics and root Journal of Crop Improvement 2011; 25: 728 - 41.
characteristics of safflower (Carthamus tinctorius 32. Limpanavech P, Chaiyasuta S, Vongpromek R,
L.). Agriculture and Plant Breeding Science Pichyangkura R, Khunwasi C, Chadchanwan S,
Eleventh Congress. 2010. Lotrakul P, Bunjongrat R, Chaidee A and
24. Hussaini Begum M, Taheri GH, Vaezi Kakhaki Bangyeekhun T. Effect of chitosan on floral
MR and Tlaty M. Foliar application of chitosan on production, gene expression and anatomical
growth and morphological characteristics of changes in the Dendrobium orchid. Science
marigold (Calendula officinalis). National Horticulture 2008; 116: 65 - 72.
33. Mahdavi B and Rahimi A. Seed priming with Gene Expression nd Catalase and Ascorbate
chitosan improves the germination and growth Peroxidase Enzymes Activity of Ocimum
performance of ajowan (Carum copticum) under basilicum by Chitosan. Journal of Crop
salt stress. Eurasian J. Biosci. 2013; 7: 69 - 76. Biotechnol. 2014; 6: 1 - 9.
34. Javanmardi J, Khalighi A, Kashi A, Bais HP 43. Cheng X, Zhou U and Cui X. Improvement of
and Vivanco JM. Chemical characterization of phenylethanoid glycosides biosynthesis in
basil (Ocimum basilicum L.) found in local Cistanchedeserticolacell suspension cultures by
accessions and used in traditional medicines in chitosan elicitor. Journal of Biotechnol. 2006; 121:
Iran. Journal of Agricultural and Food Chem. 253 - 60.
2002; 50: 5878 - 83. 44. Zhao J, Davis L.C. and Verpoorte R. Elicitor
35. Anderson OM and Jordheim M. The signal transduction leading to production of plant
anthocyanins. In: Flavonoids: Chemistry, secondary metabolites. Journal of Biotechnology
biochemistry and applications (eds. Anderson, O. Advances 2005; 23: 283 - 333.
M. and Markham, K. R.) CRC Press, London. 45. Jayakumar R, New N, Tokura S and Tamura
2005, pp: 471-553. H. Sulfated chitin and chitosan as novel
36. Michalak A. Phenolic compounds and their biomaterials. International Journal of Biological
antioxidant activity in plants growing under heavy Macromolecules 2007; 40 (3): 175 - 81.
metal stress. Polish J. of Environ. Stud. 2006; 15 46. Howlett B. Secondary metabolite toxins and
(4): 523 - 30. nutrition of plant pathogenic Fungi. Curr Opin. in
37. Liu J, Tian S, Meng X and Xu Y. Effects of Plant Biol. 2006; 9: 371 - 5
chitosan on control of postharvest diseases and 47. Zhang Y, Mian MR and Bouton J.H. Recent
physiological responses of tomato fruit. Journal of Molecular and Genomic Studies on Stress
Postharvest Biology. Technol. 2007; 44: 300 - 6. Tolerance of Forage and Turf Grasses. Crop Sci.
38. Palida S, Rath P and Supachitra C. Chitosan 2006; 46: 497 - 511.
Increased Phenolic Compound Contents in Tea 48. Naderi S, Fakheri B and Seraje M. Bio-
(Camellia sinensis) Leaves by Pre- and Post- stimulant effect of chitosan on some physiological
Treatments. Journal of Chitin and Chitosan and biochemical indices of Carum copticum
Science 2014; 2 (2): 93 - 8. (Carum copticum L.). Crop Sciences Research in
39. Esmaeilzadeh Bahabadi S, Sharifi M, Safaie N the Dry Areas 2014; 1 (2): 187 - 201.
and Behmanesh M. Enhancement of lignan and 49. Mahdavi B, ModarresSanavy S.A.M.,
phenylpropanoid compounds production by Aghaalikhani M and Sharifi M. Effect of water
chitosan in Linum album cell culture. 26. Plant stress and chitosan on Germination and proline of
Biology, Issue XI, 2012, page 13. seedling in safflower (Carthamus tinctorius L.).
40. Kim KW and Thomas RL. Antioxidative Journal of Crop Improvement 2011; 25: 728 - 41.
activity of chitosans with varying molecular 50. Khajeh H and Naderi S. The effect of chitosan
weights. Journal of Food Chem. 2007; 101: 308- on some antioxidant enzymes activity and
13. biochemictry characterization in Melissa (Melissa
41. Yen MT, Yang JH and Mau JL. Antioxidant officinalis). Crop Science Research in Arid
properties of chitosan from crab shells. Regions 2014; 1: 100 - 116. (In Persian)
Carbohydrate Polymers 2008; 74: 840 - 4. 51. Naderi S, Fakheri B and Esma'ilzadeh
42. Esmailzadeh Bahabadi S, Naderi S and Fakheri Bahabadi S. Chavicole methyltransferase gene
B. Increasing of Chavicol o-Methyl Transfrase expression and activity of catalase and ascorbate
180
ﻣﻬﺮﮔﺎن و ﻫﻤﻜﺎران
peroxidase -o plant (Ocimum basilicum L.) under M. Salicylic acid-induced changes to growth and
chitosan. Journal of Plant Biotechnology Crops phenolic metabolism in Matricaria chamomilla
2014; (6): 1-9. plants. Plant Cell Report 2009; 28: 135 - 43.
52. Kovacik J, Backor M, Strnad M and Repcak
223
2
211
213
103
Mehregan M (M.Sc. Student)1, Mehrafarin A (Ph.D.)2, Labbafi M.R (Ph.D.)2*, Naghdi Badi H (Ph.D.)2
Abstract
Introduction: Chitosan is one of the polysaccharides containing nitrogen which is synthesized
naturally by deacetylation reaction of chitin and is confirmed as one of the efficient biostimulants
for improvement of secondary metabolites production in medicinal plants.
Objective: To evaluate the effect of different concentrations of chitosan biostimulant on
vegetative biomass traits and secondary metabolites of Stevia plant.
Methods: The experiment was conducted in a randomized complete block design with three
replications in greenhouse conditions. The treatments were spraying of chitosan in four levels (0.05,
0.1 and 0.2 percent) and control treatment (spraying with distilled water).
Results: In this study, the obtained results of variance analysis showed that spraying of chitosan
had significant effect on leaf dry weight, shoot dry weight, leaf length (P <0.05), phenols and
rebaudiosides A (P <0.01). In this experiment, the highest fresh and dry weight of stems, leaves and
shoots were observed at 0.1% Chitosan in a way that by increasing the chitosan concentration from
0.1 to 0.2 % the decreasing trend occurred. The highest amount of phenol was recorded at 0.1%
concentration. Also, chitosan at 0.2% concentration had the maximum impact on rebaudiosides A.
Conclusion: Chitosan spraying improved vegetative biomass traits and biochemical parameters
such as rebaudiosides A in stevia plant.
210