Huntington’s disease (HD) is an autosomal dominant neurodegenerative disorder
characterized by choreic involuntary movements, decline in cognitive functions,
behavioral disturbances, and progressive neuronal death affecting primarily the striatum.
亨廷頓舞蹈病(HD)是一種常染色體顯性遺傳性神經退行性疾病,其特徵為舞蹈不自主運動,
認知功能下降,行為障礙和主要影響紋狀體的進行性神經元死亡。
失智症治療總整理Part-III(認知障礙缺鋅錳硒維它命A,建議草莓亞培安素、桂格特級完膳)
Huntington's disease (HD)
亨廷頓舞蹈病(HD)
HD patient cortices and mouse in vitro and in vivo models of HD have shown decreases
in accumulation of manganese (Mn2+).
HD患者皮質和小鼠體外和體內HD模型顯示錳(Mn2 +)積累減少。(缺錳)
Huntington's disease (HD).
亨廷頓舞蹈病
Further, we found decreased brain selenium content in human autopsy brain.
此外,我們發現人體屍檢腦中腦硒含量下降。(缺硒)
High prevalence of vitamin D deficiency and insufficiency in patients with manifest Huntington disease
顯著的亨廷頓病患者維生素D缺乏和不足的患病率高
At D2 3,4-dihydroxyphenylethylamine (dopamine) receptors in anterior pituitary tissue,
magnesium ions shifted receptors to agonist high-affinity states,
but decreased the affinity of the antagonist [3H]spiperone.
在垂體前葉組織中的D2多巴胺受體,鎂離子將受體轉變為激動劑高親和力狀態,但降低了拮抗劑的親和力。
Vitamin A functions in the regulation of the dopaminergic system in the brain and pituitary gland.
維生素A在調節腦和垂體中的多巴胺能系統中起作用。
Retinoic acids, bound to their receptors, function in the brain and pituitary gland
by regulating the expression of the dopamine receptor D2R
多巴胺受體D2R的表達而在腦和垂體中起作用
Dopamine (DA)
多巴胺(DA)
DA D2 receptor (D2R)
多巴胺(DA) D2受體(D2R)
The D2R Gene Promoter Is Induced by Retinoids.
D2R基因啟動子是由類視黃酸誘導的。
Retinoids Induce the Activity of the D2R Promoter in Transfected Cells.
視黃酸誘導轉染細胞中D2R啟動子的活性。
總結以上:
由於多巴胺受體D2可治療舞蹈樣多動,亨丁頓舞蹈症主要應該缺鎂、維它命A;而錳、硒、維它命D應該也有幫助。
補充鎂+維它命A+錳、硒、維它命D,建議一天一粒男性/女性善存綜合維它命礦物質或一天兩罐桂格特級完膳或草莓亞培安素。