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Is there anything that has it's mental benefits without being it?Sulphoraphane is a natural pesticide. It's not good.
Health benefits and possible risks of broccoli - an overview. - PubMed - NCBI
Cruciferous plants: phytochemical toxicity versus cancer chemoprotection. - PubMed - NCBI
Anti-angiogenic effects of dietary isothiocyanates: mechanisms of action and implications for human health. - PubMed - NCBI
decreased anxiety and mental fatigueNot sure which mental benefits you are referring to there
Sulphoraphane is a natural pesticide. It's not good.
Health benefits and possible risks of broccoli - an overview. - PubMed - NCBI
Cruciferous plants: phytochemical toxicity versus cancer chemoprotection. - PubMed - NCBI
Anti-angiogenic effects of dietary isothiocyanates: mechanisms of action and implications for human health. - PubMed - NCBI
I dunno about hatred..."However, recent in vitro and experimental animal studies indicate that broccoli, its extracts and the glucosinolate-derived degradation products might also have undesirable effects, especially genotoxic activities."
Health benefits and possible risks of broccoli - an overview. - PubMed - NCBI
Vegetable hatred is justified.
I am interested in things that help with autism, as I think some degree of it is suffered by millions of people.
Proc Natl Acad Sci U S A. 2014 Oct 28;111(43):15550-5. doi: 10.1073/pnas.1416940111. Epub 2014 Oct 13.
Sulforaphane treatment of autism spectrum disorder (ASD).
Singh K1, Connors SL2, Macklin EA3, Smith KD4, Fahey JW5, Talalay P6, Zimmerman AW7.
Author information
Abstract
Autism spectrum disorder (ASD), characterized by both impaired communication and social interaction, and by stereotypic behavior, affects about 1 in 68, predominantly males. The medico-economic burdens of ASD are enormous, and no recognized treatment targets the core features of ASD. In a placebo-controlled, double-blind, randomized trial, young men (aged 13-27) with moderate to severe ASD received the phytochemical sulforaphane (n = 29)--derived from broccoli sprout extracts--or indistinguishable placebo (n = 15). The effects on behavior of daily oral doses of sulforaphane (50-150 µmol) for 18 wk, followed by 4 wk without treatment, were quantified by three widely accepted behavioral measures completed by parents/caregivers and physicians: the Aberrant Behavior Checklist (ABC), Social Responsiveness Scale (SRS), and Clinical Global Impression Improvement Scale (CGI-I). Initial scores for ABC and SRS were closely matched for participants assigned to placebo and sulforaphane. After 18 wk, participants receiving placebo experienced minimal change (<3.3%), whereas those receiving sulforaphane showed substantial declines (improvement of behavior): 34% for ABC (P < 0.001, comparing treatments) and 17% for SRS scores (P = 0.017). On CGI-I, a significantly greater number of participants receiving sulforaphane had improvement in social interaction, abnormal behavior, and verbal communication (P = 0.015-0.007). Upon discontinuation of sulforaphane, total scores on all scales rose toward pretreatment levels. Dietary sulforaphane, of recognized low toxicity, was selected for its capacity to reverse abnormalities that have been associated with ASD, including oxidative stress and lower antioxidant capacity, depressed glutathione synthesis, reduced mitochondrial function and oxidative phosphorylation, increased lipid peroxidation, and neuroinflammmation.
Glob Adv Health Med. 2017 Oct 26;6:2164957X17735826. doi: 10.1177/2164957X17735826. eCollection 2017.
Sulforaphane from Broccoli Reduces Symptoms of Autism: A Follow-up Case Series from a Randomized Double-blind Study.
Lynch R1, Diggins EL1, Connors SL1, Zimmerman AW1,2,3,4,5, Singh K1, Liu H6,7, Talalay P6,7, Fahey JW6,7,8,9.
Author information
Abstract
INTRODUCTION:
Autism spectrum disorder (ASD) affects 1 in 68 children, is characterized by impaired social interaction and communication as well as restricted or repetitive behaviors, and varies widely with respect to its causes and presentations. There are no validated pharmacologic treatments for the core symptoms of ASD. The social, medical, and economic burdens of ASD on families and caregivers are profound. We recently showed in a small clinical trial that sulforaphane (SF) from broccoli sprouts could significantly reduce the behavioral symptoms of ASD.
METHODS:
After we completed the intervention phase of the original trial (2011-2013), many caregivers used over-the-counter dietary SF supplements in order to attempt to maintain improvements similar to those noted during the intervention. We periodically followed the progress of study participants through the summer of 2016.
RESULTS:
Families of 16 of the 26 subjects who received SF as part of the original study responded to requests for further information. Of these subjects, 6 did not continue taking SF supplements after the study. Nine of the 16 subjects are still taking an SF supplement and a 10th planned to. We present the edited testimonials of their caregivers in this case series.
CONCLUSIONS:
Many parents and caregivers articulated the positive effects of SF, both during the intervention phase and in the ensuing 3 years reported herein. These observations may contribute to understanding ASD and to treatments that may alleviate some of its symptoms. Diet- and supplement-based therapies deserve careful consideration for their potential to provide vital clinical as well as biochemical information about ASD.
KEYWORDS:
glucoraphanin; glucosinolate; isothiocyanate; prevention
April 10, 2018; 90 (15 Supplement) APRIL 22, 2018
Sulforaphane Treatment of Children with Autism Spectrum Disorder (ASD) – A Progress Report (N1.002)
Andrew Zimmerman, Eileen Diggins, Susan Connors, Kanwaljit Singh
First published April 9, 2018,
Abstract
Objective: Study the safety, clinical effects and mechanisms of action of sulforaphane in ASD.
Background: Direct treatment of underlying mechanisms in ASD is limited. The “fever effect” in ASD, in which febrile illness temporarily ameliorates disordered behavior, may offer a clinical clue. Fever stimulates heat shock proteins (HSP) and cellular stress responses, leading to improved synaptic function and long-range connectivity. Expression of gene transcription by NFE2L2 (Nrf2), which is reduced in ASD, also increases during fever. Sulforaphane (SF), an isothiocyanate obtained from broccoli sprouts, induces HSP and Nrf2 as well as “cell-protective” responses that may benefit ASD through common cellular mechanisms underlying heterogeneous phenotypes.
Design/Methods: This is a randomized, double-blind, placebo-controlled phase-2 clinical trial to test the safety and efficacy of oral SF in 50 children (age 3–12 years) with ASD. Treatment period is 30 weeks, with study-visits at screening, 7, 15, 22, 30 and 36 weeks. The first 15 weeks are double-blind, 1:1 placebo-controlled, and the second 15 weeks are open-label with all participants receiving SF. Ohio Autism Clinical Global Impressions Scale – Severity and Improvement (OACIS-S and I), Aberrant Behavior Checklist (ABC) and Social Responsiveness Scale (SRS) are administered at each study visit. Samples are collected for clinical and research lab studies at each visit.
Results: To date, we have enrolled 46 participants in the study; 24 participants have completed the trial, and 22 are actively enrolled. A preliminary analysis of the OACIS-I showed that 26% participants were much/very much improved at 7 weeks, 38% at 15 weeks, 64% at 22 weeks, and 64% at 30 weeks. Most common adverse events so far are insomnia (17%), flatulence (15%) and constipation (13%). Enrollment is expected to be complete in November, 2017, and full results after July, 2018.
Conclusions: Our preliminary results show that sulforaphane appears to be safe and effective in children with ASD.
Study Supported by: United States Department of Defense
Disclosure: Dr. Zimmerman has nothing to disclose. Dr. Diggins has nothing to disclose. Dr. Connors has nothing to disclose. Dr. Singh has nothing to disclose.
I've been reading a lot about sulforaphane and autism lately and came to the conclusion that this is probably one of the most promising treatment strategies.
In 2014, there was this randomized controlled study
Later, a follow up study was conducted on the same subjects:
The same group is currently finishing a larger trial with 50 boys and girls (3-12 years):
Sulforaphane Treatment of Children With Autism Spectrum Disorder (ASD) - Full Text View - ClinicalTrials.gov
Just two months ago, they published preliminary results in a conference proceeding. They report that 64% of the children receiving sulforaphane were much or very much improved after 30 weeks:
Two further trials are currently under way. One will include 120 participants and the other 40 participants.
A 12-weeks Study to Evaluate Sulforaphane in Treatment of Autism Spectrum Disorder - Full Text View - ClinicalTrials.gov
Sulforaphane in a New Jersey (NJ) Population of Individuals With Autism - Full Text View - ClinicalTrials.gov
At the recent AutismOne conference, Dr. Jihoon Kim shared his experience on the use of sulforaphane in children with autism. Check out this video, where he presents some astonishing cases:
Abstract said:There is robust epidemiological evidence for the beneficial effects of broccoli consumption on health, many of them clearly mediated by the isothiocyanate sulforaphane. Present in the plant as its precursor, glucoraphanin, sulforaphane is formed through the actions of myrosinase, a β-thioglucosidase present in either the plant tissue or the mammalian microbiome. Since first isolated from broccoli and demonstrated to have cancer chemoprotective properties in rats in the early 1990s, over 3000 publications have described its efficacy in rodent disease models, underlying mechanisms of action or, to date, over 50 clinical trials examining pharmacokinetics, pharmacodynamics and disease mitigation. This review evaluates the current state of knowledge regarding the relationships between formulation (e.g., plants, sprouts, beverages, supplements), bioavailability and efficacy, and the doses of glucoraphanin and/or sulforaphane that have been used in pre-clinical and clinical studies. We pay special attention to the challenges for better integration of animal model and clinical studies, particularly with regard to selection of dose and route of administration. More effort is required to elucidate underlying mechanisms of action and to develop and validate biomarkers of pharmacodynamic action in humans. A sobering lesson is that changes in approach will be required to implement a public health paradigm for dispensing benefit across all spectrums of the global population.