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蛋白质/氨基酸danbaizhianjisuan

5-羟色氨酸(2)

时间:2020-12-16 20:19 阅读:770 来源:朴诺健康研究院

5-羟色氨酸

5-羟色氨酸的功能

5-羟色氨酸在人体内用于合成5-羟色胺。5-羟色胺是一种维持机体正常神经和大脑功能的物质。

5-羟色胺在睡眠、情绪控制、疼痛控制、炎症、肠蠕动以及其他机体功能上发挥着重要作用。[1]

5-羟色氨酸的分布

5-羟色氨酸在一般饮食中摄入的量并不多。人体可以从左旋色氨酸(一种食物蛋白中含量丰富的氨基酸)合成5-羟色氨酸。可是,吃含有左旋色氨酸的食物却不会增加5-羟色氨酸水平。5-羟色氨酸补充剂是从一种西非药用植物的果实加纳籽中提取而来。

5-羟色氨酸认为与以下疾病有关(以下所有信息适用于个体化健康情况):

分类健康情况
次选

抑郁、纤维肌痛、失眠、偏头痛、紧张性头痛、间质性膀胱炎、术前和术后康复、体重减轻和肥胖

其他

躁狂抑郁症、进食障碍病、帕金森(与左旋多巴合用)、季节性情感障

首选:有可靠和相对一致的科研数据证明其对健康有显著改善。

次选:各有关科研结果相互矛盾、证据不充分或仅能初步表明其可改善健康状况或效果甚微。

其它:对草药来说,仅有传统用法可支持其应用,但尚无或仅有少量科学证据可证明其疗效。对营养补充剂来说,无科学证据支持和/或效果甚微。

哪些人可能会缺乏?

情绪上的紊乱(如抑郁和紧张)认为与大脑内的5-羟色氨酸平衡失调有关[2]。患有纤维肌痛的病人血中5-羟色氨酸水平含量较低[3 4 5]。5-羟色氨酸补充剂可以提高这些病人5-羟色胺的水平。偏头痛与血液中5-羟色胺功能失常有关[6],5-羟色氨酸也可以纠正这一异常。失眠认为与大脑组织内色氨酸缺乏有关[7],因此也可以通过补充5-羟色氨酸来纠正。

一般需要多少5-羟色氨酸?

在一项对照试验中发现,每天服用5-羟色氨酸300毫克对于减轻纤维肌痛的症状、包括疼痛、晨僵、睡眠紊乱和焦虑。[8]

治疗抑郁,每天300毫克通常有效。[9 10 11]睡前服用100毫克的5-羟色氨酸用于提高睡眠的深度和持久性有一定的疗效,这在一项安慰剂对照试验中证实可以治疗失眠。[12]每天400~600毫克可以减少偏头痛的发生频率和强度。[13 14 15 16 17]对于紧张性头痛,每天服用3次100毫克的5-羟色氨酸可以明显减少止疼药的剂量,但是对于疼痛的强度和持续时间却没有明显改善。[18]

每天服用600~900毫克会导致食欲下降和体重减轻(平均12周减少11磅)。[19 20]另一项试验中每天服用750毫克的5-羟色氨酸可以减少碳水化合物和脂肪摄入,以达到减肥效果。[21]

是否有副作用和药物相互作用?

以上的一些临床试验中发现,一些人服用大剂量的5-羟色氨酸会出现胃肠道反应(如恶心),少见的会出现头痛、易困、肌肉疼痛或紧张。一种称为“X 峰”的物质在一些过度服用5-羟色氨酸的人中有一定的含量。[22 23 24]许多研究认为这种物质与1989年色氨酸中毒事件有关。[25 26 27]但是,是否真的是这种物质导致的毒性反应还存在着许多问题无法解答。[28 29 30 31 32 33 34 35 ]尽管有两篇文章报道了服用5-羟色氨酸出现了因左旋多巴污染导致的毒性反应症状,[36 37]但是关于5-羟色氨酸或“X峰”的毒性反应还只是推测而已。尽管最近已经鉴定出“X峰”的结构,但是关于这种物质引起毒性反应或疾病的证据还不足。[38]

在几内亚猪的试验中发现摄入高剂量的5-羟色氨酸会导致肌肉抽搐。[39]而在老鼠则出现了肌肉抽搐[40]和腹泻[41]。给老鼠注射5-羟色氨酸还会引起肾损害[42]。还没有关于这些症状在人类的报道。血清素综合征是由于过多摄入5-羟色胺出现的一系列症状,但还没有关于服用5-羟色氨酸补充剂出现这一症状的报道[43]。尽管理论上会出现,但是摄入多少会引起毒性反应还不十分清楚。

5-羟色氨酸不应与抗抑郁药、减肥药、其他5-羟色胺修饰剂或导致肝损害的药物一起服用,因为这些药物会引起5-羟色氨酸作用过度。肝损害的病人不能正常调节5-羟色氨酸,以及那些患有自身免疫疾病的人如硬皮病敏感性更高。[44]因此,这些病人应该在专业医生的指导下才能服用。怀孕期和哺乳期能否服用5-羟色氨酸还不清楚。

许多药物都与5-羟色氨酸相互作用。参见药物间相互作用章节。

参考文献

1. Guyton AC, Hall JE. Textbook of Medical Physiology, 9th ed. Philadelphia: W. B. Saunders, 1996.

2. van Praag HM, Lemus C. Monoamine precursors in the treatment of psychiatric disorders. Nutrition and the Brain, vol. 7, eds. RJ Wurtman, JJ Wurtman. New York: Raven Press, 1986 [review].

3. Russell IJ, Michalek JE, Vipraio GA, et al. Platelet 3H-imipramine uptake receptor density and serum serotonin levels in patients with fibromyalgia/fibrositis syndrome. J Rheumatol 1992;19:90–4.

4. Yunus MB, Dailey JW, Aldag JC, et al. Platelet 3H-imiprimine uptake receptor density and serum serotonin levels in patients with fibromyalgia/fibrositis syndrome. J Rheumatol 1992;19:104–9.

5. Wolfe F, Russell IJ, Vipraio G, et al. Serotonin levels, pain threshold, and fibromyalgia symptoms in the general population. J Rheumatol 1997;24:555–9.

6. Kimball RW, Friedman AP, Vallejo E. Effect of serotonin in migraine patients. Neurology 1960;10:107–11.

7. Schneider-Helmert D, Spinweber CL. Evaluation of L-tryptophan for treatment of insomnia: A review. Psychopharmacology (Berlin) 1986;89(1):1–7.

8. Caruso I, Sarzi Puttini P, Cazzola M, Azzolini V. Double-blind study of 5-hydroxytryptophan versus placebo in the treatment of primary fibromyalgia syndrome. J Int Med Res 1990;18:201–9.

9. Byerley WF, Judd LL, Reimherr FW, Grosser BI. 5-hydroxytryptophan: A review of its antidepressant efficacy and adverse effects . J Clin Psychopharmacol 1987;7:127–37 [review].

10. Zmilacher K, Battegay R, Gastpar M. L-5-hydroxytryptophan alone and in combination with a peripheral decarboxylase inhibitor in the treatment of depression. Neuropsychobiology 1988;20:28–35.

11. Poldinger W, Calanchini B, Schwarz W. A functional-dimensional approach to depression: serotonin deficiency as a target syndrome in a comparison of 5-hydroxytryptophan and fluvoxamine. Psychopathology 1991;24(2):53–81.

12. Soulairac A, Lambinet H. Etudes cliniques de líaction du precurseur de la serotonine le L-5-hydroxy-tryptophane, sur les troubles du sommeil. Schweiz Bundschau Med (PRAXIS) 1998;77(34a):19–23 [in French].

13. De Benedittis G, Massei R. 5-HT precursors in migraine prophylaxis: a double-blind cross-over study with L-5-hydroxytryptophan versus placebo. Clin J Pain 1986;3:123–9.

14. Titus F, Davalos A, Alom J, Codina A. 5-hydroxytryptophan versus methysergide in the prophylaxis of migraine. Eur Neurol 1986;25:327–9.

15. Maissen CP, Ludin HP. Comparison of the effect of 5-hydroxytryptophan and propranolol in the interval treatment of migraine. Schweizerische Medizinische Wochenschrift /Journal Suisse de Medecine 1991;121:1585–90 [in German].

16. Mathew NT. 5-hydroxytryptophan in the prophylaxis of migraine. Headache 1978;18:111–3.

17. De Giorgis G, Miletto R, Iannuccelli M, et al. Headache in association with sleep disorders in children: a psychodiagnostic evaluation and controlled clinical study ? L-5-HTP versus placebo. Drugs Exptl Clin Res 1987;13(7):425–33.

18. Ribeiro CA. L-5-Hydroxytryptophan in the prophylaxis of chronic tension-type headache: a double-blind, randomized, placebo-controlled study. Headache 2000;40:451–6.

19. Ceci F, Cangiano C, Cairella M, et al. The effects of oral 5-hydroxytryptophan administration on feeding behavior in obese adult female subjects.J Neural Transm 1989;76(2):109–17.

20. Cangiano C, Ceci F, Cascino A, et al. Eating behavior and adherence to dietary prescriptions in obese adult subjects treated with 5-hydroxytryptophan. Am J Clin Nutr 1992;56:863–7.

21. Cangiano C, Laviano A, Del Ben M, et al. Effects of oral 5-hydroxy-tryptophan on energy intake and macronutrient selection in non-insulin dependent diabetic patients. Int J Obes Relat Metab Disord 1998;22:648–54.

22. Williamson BL, Benson LM, Tomlinson AJ, et al. On-line HPLC-tandem mass spectrometry analysis of contaminants of L-tryptophan associated with the onset of the eosinophilia-myalgia syndrome. Toxicol Lett 1997;92:139–48.

23. Williamson BL, Klarskov K, Tomlinson AJ, et al. Problems with over-the-counter 5-hydroxy-L-tryptophan. Nat Med 1998;4:983.

24. Williamson BL, Tomlinson AJ, Mishra PK, et al. Structural characterization of contaminants found in commercial preparations of melatonin: similarities to case-related compounds from L-tryptophan associated with eosinophilia-myalgia syndrome. Chem Res Toxicol 1998;11:234–40.

25. Belongia EA, Hedberg CW, Gleich GJ, et al. An investigation of the cause of the eosinophilia-myalgia syndrome associated with tryptophan use. N Engl J Med 1990;323:357–65.

26. Martin RW, Duffy J, Engel AG, et al. The clinical spectrum of the eosinophilia-myalgia syndrome associated with L-tryptophan ingestion. Clinical features in 20 patients and aspects of pathophysiology. Ann Intern Med 1990;113:124–34.

27. Mayeno AN, Lin F, Foote CS, et al. Characterization of “peak E,” a novel amino acid associated with eosinophilia-myalgia syndrome. Science 1990;250:1707–8.

28. Belongia EA, Hedberg CW, Gleich GJ, et al. An investigation of the cause of the eosinophilia-myalgia syndrome associated with tryptophan use. N Engl J Med 1990;323:357–65.

29. Mayeno AN, Lin F, Foote CS, et al. Characterization of “peak E,” a novel amino acid associated with eosinophilia-myalgia syndrome. Science 1990;250:1707–8.

30. Reinauer S, Plewig G. [Eosinophilia-myalgia syndrome]. Hautarzt 1991;42(3):137–9 [in German].

31. Toyo’oka T, Yamazaki T, Tanimoto T, et al. Characterization of contaminants in EMS-associated L-tryptophan samples by high-performance liquid chromatography. Chem Pharm Bull (Tokyo) 1991;39(3):820–2.

32. Trucksess MW, Thomas FS, Page SW. High-performance liquid chromatographic determination of 1,1’-ethylidenebis(L-tryptophan) in L-tryptophan preparations. J Pharm Sci 1994;83(5):720–2.

33. Trucksess MW. Separation and isolation of trace impurities in L-tryptophan by high-performance liquid chromatography. J Chromatogr 1993;630(1–2):147–50.

34. Ito J, Hosaki Y, Torigoe Y, Sakimoto K. Identification of substances formed by decomposition of peak E substance in tryptophan. Food Chem Toxicol 1992;30(1):71–81.

35. Castot A, Bidault I, Bournerias I, et al. [“Eosinophilia-myalgia” syndrome due to L-tryptophan containing products. Cooperative evaluation of French Regional Centers of Pharmacovigilance. Analysis of 24 cases]. Therapie 1991;46(5):355–65 [in French].

36. Michelson D, Page SW, Casey R, et al. An eosinophilia-myalgia syndrome related disorder associated with exposure to L-5-hydroxytryptophan. J Rheumatol 1994;21:2261–5.

37. Sternberg EM, Van Woert MH, Young SN, et al. Development of a scleroderma-like illness during therapy with L-5-hydroxytryptophan and carbidopa. N Engl J Med 1980;303(14):782–7.

38. Johnson KL, Klarskov K, Benson LM, et al. Presence of peak X and related compounds: the reported contaminant in case related 5-Hydroxy-L-tryptophan associated with eosinophilia-myalgia syndrome. J Rheumatol 1999;26(12):2714–7.

39. Hagan JJ, Hatcher JP, Slade PD. The role of 5-HT1D and 5-HT1A receptors in mediating 5-hydroxytryptophan induced myoclonic jerks in guinea pigs. Eur J Pharmacol 1995;294:743–51.

40. Green AR, Johnson P, Mountford JA, Nimgaonkar VL. Some anticonvulsant drugs alter monoamine mediated behaviour in mice in ways similar to electroconvulsive shock; implications for antidepressant therapy. Br J Pharmacol 1985;84:337–46.

41. Bourin M, Hascoet M, Deguiral P. 5-HTP induced diarrhea as a carcinoid syndrome model in mice? Fundam Clin Pharmacol 1996;10:450–7.

42. Hirai M, Nakajima T. Biochemical studies on the mechanism of difference in the renal toxicity of 5-hydroxy-L-tryptophan between Sprague Dawley and Wistar rats. J Biochem (Tokyo) 1979;86:907–13.

43. Martin TG. Serotonin syndrome. Ann Emerg Med 1996;28:520–6.

44. Sternberg EM, Van Woert MH, Young SN, et al. Development of a scleroderma-like illness during therapy with L-5-hydroxytryptophan and carbidopa. N Engl J Med 1980;303:782–7.