墨西哥鼠尾草

出自台灣有毒中草藥毒性資料庫

(修訂版本間的差異)
跳轉到: 導航, 搜尋
(參考文獻)
(參考文獻)
第81行: 第81行:
== '''參考文獻''' ==
== '''參考文獻''' ==
-
1. Vortherms TA, Roth BL. Salvinorin A: from natural product to human therapeutics. Mol Interv. 2006 Oct;6(5):257-65.
+
1. Vortherms TA, Roth BL. [http://www.ncbi.nlm.nih.gov/pubmed/17035666 Salvinorin A: from natural product to human therapeutics.] ''Molecular interventions'' 2006;6(5):257-65.
-
2. Khey DN, Miller BL, Griffin OH. Salvia divinorum use among a college student sample. J Drug Educ. 2008;38(3):297-306.
+
2. Khey DN, Miller BL, Griffin OH. [https://www.ncjrs.gov/App/publications/Abstract.aspx?id=247970 Salvia divinorum use among a college student sample.] ''Journal of Drug Education'' 2008;38(3):297-306.
-
3. Lange JE, Reed MB, Croff JM, Clapp JD. College student use of Salvia divinorum. Drug Alcohol Depend. 2008 Apr 1;94(1-3):263-6.
+
3. Lange JE, Reed MB, Croff JM, Clapp JD. [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2267695/ College student use of Salvia divinorum.] ''Drug and alcohol dependence'' 2008;94(1-3):263-6.
-
4. Wu LT, Woody GE, Yang C, Li JH, Blazer DG. Recent national trends in Salvia divinorum use and substance-use disorders among recent and former Salvia divinorum users compared with nonusers. Subst Abuse Rehabil. 2011 Apr;2011(2):53-68.
+
4. Wu LT, Woody GE, Yang C, Li JH, Blazer DG. [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3122136/ Recent national trends in Salvia divinorum use and substance-use disorders among recent and former Salvia divinorum users compared with nonusers.] ''Journal of Substance Abuse and Rehabilitation'' 2011;2011(2):53-68.
-
5. Giroud C, Felber F, Augsburger M, Horisberger B, Rivier L, Mangin P. Salvia divinorum: an hallucinogenic mint which might become a new recreational drug in Switzerland. Forensic Sci Int. 2000 Aug 14;112(2-3):143-50.
+
5. Giroud C, Felber F, Augsburger M, Horisberger B, Rivier L, Mangin P. [http://www.ncbi.nlm.nih.gov/pubmed/10940599 Salvia divinorum: an hallucinogenic mint which might become a new recreational drug in Switzerland.] ''Forensic Science International'' 2000;112(2-3):143-50.
-
6. Griffin OH, Miller BL, Khey DN. Legally high? Legal considerations of Salvia divinorum. J Psychoactive Drugs. 2008 Jun;40(2):183-91.
+
6. Griffin OH, Miller BL, Khey DN. [http://www.ncbi.nlm.nih.gov/pubmed/18720668 Legally high? Legal considerations of Salvia divinorum.] ''Journal of psychoactive drugs'' 2008;40(2):183-91.
7. Washington DC. Salvia divinorum and salvinorin A. Drug Enforcement Administration; 2008; Available from: http://www.justice.gov/dea/concern/salvia_divinorum_one_pager.pdf.
7. Washington DC. Salvia divinorum and salvinorin A. Drug Enforcement Administration; 2008; Available from: http://www.justice.gov/dea/concern/salvia_divinorum_one_pager.pdf.
-
8. Valdes LJ, 3rd, Diaz JL, Paul AG. Ethnopharmacology of ska Maria Pastora (Salvia divinorum, Epling and Jativa-M.). J Ethnopharmacol. 1983 May;7(3):287-312.
+
8. Valdes LJ, 3rd, Diaz JL, Paul AG. [http://www.ncbi.nlm.nih.gov/pubmed/6876852 Ethnopharmacology of ska Maria Pastora (Salvia divinorum, Epling and Jativa-M.).] ''Journal of Ethnopharmacology'' 1983;7(3):287-312.
-
9. Paulzen M, Grunder G. Toxic psychosis after intake of the hallucinogen salvinorin A. J Clin Psychiatry. 2008 Sep;69(9):1501-2.
+
9. Paulzen M, Grunder G. [http://www.ncbi.nlm.nih.gov/pubmed/19193352 Toxic psychosis after intake of the hallucinogen salvinorin A. Toxic psychosis after intake of the hallucinogen salvinorin A.] ''Journal of Clinical Psychiatry'' 2008;69(9):1501-1502.
-
10. Vohra R, Seefeld A, Cantrell FL, Clark RF. Salvia divinorum: exposures reported to a statewide poison control system over 10 years. J Emerg Med. 2009 Sep 16.
+
10. Vohra R, Seefeld A, Cantrell FL, Clark RF. [http://www.ncbi.nlm.nih.gov/pubmed/19765944 Salvia divinorum: exposures reported to a statewide poison control system over 10 years.] J Emerg Med. 2011;40(6):643-650
-
11. Kutrzeba L, Dayan FE, Howell J, Feng J, Giner JL, Zjawiony JK. Biosynthesis of salvinorin A proceeds via the deoxyxylulose phosphate pathway. Phytochemistry. 2007 Jul;68(14):1872-81.
+
11. Kutrzeba L, Dayan FE, Howell J, Feng J, Giner JL, Zjawiony JK. [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2065853/ Biosynthesis of salvinorin A proceeds via the deoxyxylulose phosphate pathway.] Phytochemistry. 2007;68(14):1872-81.
-
12. Pfeiffer A, Brantl V, Herz A, Emrich HM. Psychotomimesis mediated by kappa opiate receptors. Science. 1986 Aug 15;233(4765):774-6.
+
12. Pfeiffer A, Brantl V, Herz A, Emrich HM. [http://www.ncbi.nlm.nih.gov/pubmed/3016896 Psychotomimesis mediated by kappa opiate receptors.] Science. 1986;233(4765):774-6.
-
13. Beguin C, Richards MR, Li JG, Wang Y, Xu W, Liu-Chen LY, et al. Synthesis and in vitro evaluation of salvinorin A analogues: effect of configuration at C(2) and substitution at C(18). Bioorg Med Chem Lett. 2006 Sep 1;16(17):4679-85.
+
13. Beguin C, Richards MR, Li JG, Wang Y, Xu W, Liu-Chen LY, et al. [http://www.ncbi.nlm.nih.gov/pubmed/16777411 Synthesis and in vitro evaluation of salvinorin A analogues: effect of configuration at C(2) and substitution at C(18).] Bioorg Med Chem Lett. 2006;16(17):4679-85.
-
14. Tsujikawa K, Kuwayama K, Miyaguchi H, Kanamori T, Iwata YT, Yoshida T, et al. Determination of salvinorin A and salvinorin B in Salvia divinorum-related products circulated in Japan. Forensic Sci Int. 2008 Sep 18;180(2-3):105-9.
+
14. Tsujikawa K, Kuwayama K, Miyaguchi H, Kanamori T, Iwata YT, Yoshida T, et al. [http://www.ncbi.nlm.nih.gov/pubmed/18768273 Determination of salvinorin A and salvinorin B in Salvia divinorum-related products circulated in Japan.] Forensic Sci Int. 2008;180(2-3):105-9.
[http://tcm-toxic.kmu.edu.tw/index.php/%E5%A4%A7%E6%88%9F%E7%A7%91 返回上一頁]
[http://tcm-toxic.kmu.edu.tw/index.php/%E5%A4%A7%E6%88%9F%E7%A7%91 返回上一頁]

在2011年11月12日 (六) 11:57所做的修訂版本

[返回上一頁]

目錄

基本資料

科別

唇形科 Lamiaceae

屬名

鼠尾草屬 Salvia

中文學名

墨西哥鼠尾草

拉丁學名

Salvia divinorum L.

英文名稱

Diviner's Sage, Ska María Pastora, Seer's Sage, Salvia

中文俗名


植物圖片

[[檔案:|300px|]]


[[檔案:|300px|]]


[[檔案:‎|300px|]]


[[檔案:|300px|]]


[[檔案:|300px|]]


[[檔案:|300px|]]


墨西哥鼠尾草簡介

Salvia divinorum為多年生的草本植物。在國外除了作為傳統的民俗用藥以外,Salvia divinorum具有至幻覺之作用,因此曾被”民間術士”作為一種會產生迷幻作用的精神占卜藥物(1)。Salvia divinorum會造成與ketamine相類似的迷幻作用(例:“進入另一個現實世界“、“精神與身體分離“以及“時空錯位“),因此近幾年來Salvia divinorum的使用在歐美國家相當的風行,尤其在年輕族群間相當的盛行(2-4)。過去文獻報導指出,Salvia divinorum的使用逐漸取代了大麻(5)。在美國有一位青少年因為使用Salvia divinorum而導致自殺死亡的事件,使得當地政府對於此案例相當的重視(6)。過去文獻報導也指出使用Salvia divinorum後會可能導致使用者產生精神疾病。目前已經有許多國家對於Salvia divinorum進行控管或是立法,美國也從原本2008年有立法管制Salvia divinorum的13個州,在2010年時提升至16個州進行管制(7)。


外觀簡述

其生長高度可超過1米,為中空方形莖

葉為卵形、齒狀以及十字對生長約15厘米長

花為白花,螺旋狀(30厘米)花序,紫色花萼,很少開花。

果實

[5,8]

產地

原產於墨西哥卡瓦州,Sierra Madre東方的Mazatec 區。

毒性研究

在過去有一案例報告中指出,一位18歲有使用大麻歷史的年輕女性,抽食Salvia divinorum葉後造成了長時間的精神障礙及精神分裂症(9)。在2011年的一篇研究比較曾經使用過/正在使用Salvia divinorum族群與未曾使用過之族群,發現曾經使用過/正在使用的族群患有憂鬱症機率較未曾使用過之族群高達了1.4倍之多(4)。雖然不前並無急性毒性的案例報告或是研究,但據上述的文獻報導,可發現長期使用Salvia divinorum可能會導致精神症狀的發生。

  • 症狀

使用Salvinorin A後會產生一些症狀,像是混亂、定向障礙、幻覺、眩暈或頭暈、滿臉通紅的感覺、心動過速、震顫、心悸、高血壓、噁心、嘔吐等。有時會因依賴的劑量或是使用途徑而造成一些負面感受,像是過於強烈的經驗、恐懼、恐怖、恐慌、排汗增加、難以整合的經驗(9, 10)。

  • 有毒成份

Salvinorin A屬無含氮二萜類(neoclerodane diterpenoid)的化合物是Salvia divinorum之主要產生幻覺之成分(11)。Salvinorin A所產生的迷幻作用與phencyclidine及ketamine相同,是目前青少年爛用Salvia divinorum的主要成分。

  • 機轉

在1986年的一篇文件指出κ-opioid receptor致效劑會導致與phencyclidine及ketamine相同迷幻作用的發生以及造成精神症狀的發生(12)。Salvinorin A對於阿片受體κ-opioid receptor具有非常高的親和力,但對於μ-opioid receptor並無作用,為阿片類藥物以外具有阿片受體有高親和力之二萜化合物。在結構上以碳4位置上的甲基脂(methyl ester)以及碳12位置上的呋喃環(furan ring)為對於κ-receptor具選擇性的結構(1, 13)。

  • 中毒劑量

文獻指出,吸食40-70 mg的Salvia divinorum(約200–500 µg的Salvinorin A)即可達到迷幻效果(14)。雖然目前沒有文獻指出使用Salvia divinorum是否有明確的毒性及毒性劑量,但在長期使用下是可能造成精神疾病的產生(4)。

毒性分級

Class B1

參考文獻

1. Vortherms TA, Roth BL. Salvinorin A: from natural product to human therapeutics. Molecular interventions 2006;6(5):257-65.

2. Khey DN, Miller BL, Griffin OH. Salvia divinorum use among a college student sample. Journal of Drug Education 2008;38(3):297-306.

3. Lange JE, Reed MB, Croff JM, Clapp JD. College student use of Salvia divinorum. Drug and alcohol dependence 2008;94(1-3):263-6.

4. Wu LT, Woody GE, Yang C, Li JH, Blazer DG. Recent national trends in Salvia divinorum use and substance-use disorders among recent and former Salvia divinorum users compared with nonusers. Journal of Substance Abuse and Rehabilitation 2011;2011(2):53-68.

5. Giroud C, Felber F, Augsburger M, Horisberger B, Rivier L, Mangin P. Salvia divinorum: an hallucinogenic mint which might become a new recreational drug in Switzerland. Forensic Science International 2000;112(2-3):143-50.

6. Griffin OH, Miller BL, Khey DN. Legally high? Legal considerations of Salvia divinorum. Journal of psychoactive drugs 2008;40(2):183-91.

7. Washington DC. Salvia divinorum and salvinorin A. Drug Enforcement Administration; 2008; Available from: http://www.justice.gov/dea/concern/salvia_divinorum_one_pager.pdf.

8. Valdes LJ, 3rd, Diaz JL, Paul AG. Ethnopharmacology of ska Maria Pastora (Salvia divinorum, Epling and Jativa-M.). Journal of Ethnopharmacology 1983;7(3):287-312.

9. Paulzen M, Grunder G. Toxic psychosis after intake of the hallucinogen salvinorin A. Toxic psychosis after intake of the hallucinogen salvinorin A. Journal of Clinical Psychiatry 2008;69(9):1501-1502.

10. Vohra R, Seefeld A, Cantrell FL, Clark RF. Salvia divinorum: exposures reported to a statewide poison control system over 10 years. J Emerg Med. 2011;40(6):643-650

11. Kutrzeba L, Dayan FE, Howell J, Feng J, Giner JL, Zjawiony JK. Biosynthesis of salvinorin A proceeds via the deoxyxylulose phosphate pathway. Phytochemistry. 2007;68(14):1872-81.

12. Pfeiffer A, Brantl V, Herz A, Emrich HM. Psychotomimesis mediated by kappa opiate receptors. Science. 1986;233(4765):774-6.

13. Beguin C, Richards MR, Li JG, Wang Y, Xu W, Liu-Chen LY, et al. Synthesis and in vitro evaluation of salvinorin A analogues: effect of configuration at C(2) and substitution at C(18). Bioorg Med Chem Lett. 2006;16(17):4679-85.

14. Tsujikawa K, Kuwayama K, Miyaguchi H, Kanamori T, Iwata YT, Yoshida T, et al. Determination of salvinorin A and salvinorin B in Salvia divinorum-related products circulated in Japan. Forensic Sci Int. 2008;180(2-3):105-9.

返回上一頁

個人工具