PELI Logo
title

Stimulating Herbs in Place of Amphetamines in Adult Attention-Deficit/Hyperactivity Disorder (ADHD)

Attention-deficit/hyperactivity disorder (ADHD) is an underdiagnosed, undertreated, and often comorbid condition in adults.1 While recognised as a common childhood behavioural disorder,2 ADHD persists through to adulthood in as many as two-thirds of patients3,4 despite a general lack of awareness.1 It majorly impacts an individual’s social life and wellbeing. It is strongly linked with substance use disorder,1 wherein self-medication may be a factor.5

ADHD can be viewed as a deficiency of stimulation.6 In normal neurotransmitter physiology, a ‘brain reward cascade’ occurs. Serotonin, enkephalin and gamma-aminobutyric acid (GABA) work in concert, resulting in the release of dopamine at the nucleus accumbens7 – a crucial part of the brain reward system.8 However, in the pathophysiology of ADHD, this process is dysfunctional. The dysregulation of these neurotransmitters is caused by genetic abnormalities such as a defect in the dopamine receptor D2 (DRD2) gene. This defect decreases the number of dopamine receptor sites in reward centres and reduces the amount of dopamine produced in this area. This underlying need to increase brain dopamine to produce feelings of pleasure helps explain why individuals with ADHD engage in high-risk activities (e.g., substance use).6

Conventional medications for ADHD are psychostimulants that increase dopamine and noradrenaline in the synaptic space. These promote the release of catecholamines from presynaptic nerve terminals and block their reuptake via competitive inhibition.9,10 Notably, released catecholamines also affect α- and β-adrenergic receptor sites,9,11 with α-adrenergic receptors playing an important role in blood pressure (BP) regulation.12,13

Statistics show that as many as nearly one in every four patients with substance use disorders meet the criteria for a diagnosis of comorbid ADHD.14 Self-medicating (unknowingly) is not uncommon for the undiagnosed adult. However, while doses of prescribed stimulants are predictable, illicit drugs such as methamphetamine are not. High doses of methamphetamine induce damaging neurotoxic effects by eliciting oxidative stress within dopamine terminals and surrounding compartments.15

Herbal therapies prescribed by naturopathic practitioners can address neuroinflammation, exerting neuroprotective effects16-19 to help correct underlying neurotransmitter imbalances, alleviate symptoms and improve quality of life. As such, the clinical aim in this case was to replace synthetic forms of stimulation with stimulating herbs that could concurrently offer neuroprotective benefits.


Patient History


An adult male presented with regular use of methamphetamine. He had been using the illicit drug for around 3 years and found it helped him to feel calmer and think more clearly. The patient was a successful finance broker with very high expectations of personal achievement. His sense of self-worth was tied to his ability to provide for his family. He would purchase his supply monthly and cycle 2 weeks on 2 weeks off. For the off period, he would tolerate the withdrawal symptoms.

He then tried taking the drug without a period of abstinence for 2 months when things began to fall apart. Around the same time, his wife discovered his drug use, moved out with their children and demanded a clean drug test for him to visit his kids.

He was referred to a psychiatrist through his marriage counsellor. The patient was eventually diagnosed with ADHD and prescribed dexamphetamine. However, as a clean urine drug test was part of his marriage, he wanted to stop use of dexamphetamine as this is indistinguishable from methamphetamine in the test.


Medications


Dexamphetamine


Initial Prescription


Liquid extract: 5-10 mL three times a day


Herb
  Extract Ratio
Quantity
Korean Ginseng
  1:2
30 mL
Schisandra
  1:2
25 mL
Ginkgo
  2:1
25 mL
Rhodiola
  2:1
25 mL


105 mL


NB: 210 mL was provided for 1 week


Rationale: I consider all herbs to be stimulating. Ginkgo combined with American Ginseng (replaced with Korean Ginseng) can improve hyperactive-impulsiveness.20 Korean Red Ginseng can significantly improve inattention/hyperactivity scores.21 Ginseng phytochemicals are neuroprotective.17

1-week Follow-up

• The full amount of the liquid extract was used at a dose of 10 mL three times a day

• Felt he needed more from the herbs

• He felt tired for the first few days, experienced abdominal pain, but both resolved at the same time a few days  
  later

• Reports that he has been sleeping well

• Focused on getting better. Attending Narcotics Anonymous meetings four times weekly, deleting drug dealers’
  numbers from his phone contacts and meditating for an hour each day

• Feeling optimistic

• BP: 158/70 mmHg


Prescription changes:


o Increased dose of the liquid extract to 15 mL three times a day


Follow-up


• Ran out of the mixture for three days and had not been sleeping well since

• He wanted to get something from the pharmacy to aid his sleep (e.g., herbal sedative) but I suggested against
  this, believing that he needed stimulating during the day with the liquid extract rather than sedating at night

• Stress from an estranged wife who still was not trusting him to see his children

• Same prescription dispensed. Enough to last 10 days

Lost to follow-up.

Clinical Thoughts

Sometimes our best intentions and hopes don’t align with the client’s own expectations. Natural medicines work slowly and steadily, requiring perseverance on the patient’s behalf to get there. This case highlighted to me the importance of managing expectations, especially with substance use.


References


1. Ginsberg Y, Quintero J, Anand E, Casillas M, Upadhyaya HP. Underdiagnosis of attention-deficit/hyperactivity disorder in adult patients: a review of the literature. Prim Care Companion CNS Disord. 2014;16(3):PCC.13r01600. DOI: 10.4088/PCC.13r01600

2. Sayal K, Prasad V, Daley D, Ford T, Coghill D. ADHD in children and young people: prevalence, care pathways, and service provision. Lancet Psychiatry. 2018 Feb;5(2):175-186. DOI: 10.1016/S2215-0366(17)30167-0

3. Sibley MH, Swanson JM, Arnold LE, Hechtman LT, Owens EB, Stehli A, et al. Defining ADHD symptom persistence in adulthood: optimizing sensitivity and specificity. J Child Psychol Psychiatry. 2017 Jun;58(6):655-662. DOI: 10.1111/jcpp.12620

4. Turgay A, Goodman DW, Asherson P, Lasser RA, Babcock TF, Pucci ML, et al. Lifespan persistence of ADHD: the life transition model and its application. J Clin Psychiatry. 2012 Feb;73(2):192-201. DOI: 10.4088/JCP.10m06628

5. Wilens TE. Impact of ADHD and its treatment on substance abuse in adults. J Clin Psychiatry. 2004;65 Suppl 3:38-45.

6. Blum K, Chen ALC, Braverman ER, Comings DE, Chen TJH, Arcuri V, et al. Attention-deficit-hyperactivity disorder and reward deficiency syndrome. Neuropsychiatr Dis Treat. 2008 Oct;4(5):893-918. DOI: 10.2147/ndt.s2627

7. Blum K, Oscar-Berman M, Stuller E, Miller D, Giordano J, Morse S, et al. Neurogenetics and nutrigenomics of neuro-nutrient therapy for reward deficiency syndrome (RDS): clinical ramifications as a function of molecular neurobiological mechanisms. J Addict Res Ther. 2012 Nov;3(5):139. DOI: 10.4172/2155-6105.1000139

8. Carelli RM. The nucleus accumbens and reward: neurophysiological investigations in behaving animals. Behav Cogn Neurosci Rev. 2002 Dec;1(4):281-296. DOI: 10.1177/1534582302238338

9. Wilens TE. Effects of methylphenidate on the catecholaminergic system in attention-deficit/hyperactivity disorder. J Clin Psychopharmacol. 2008 Jun;28(3 Suppl 2):S46-53. DOI: 10.1097/JCP.0b013e318173312f

10. Seiden LS, Sabol KE, Ricaurte GA. Amphetamine: effects on catecholamine systems and behavior. Annu Rev Pharmacol Toxicol. 1993;33:639-77. DOI: 10.1146/annurev.pa.33.040193.003231

11. Lefkowitz RJ, Williams LT. Catecholamine binding to the beta-adrenergic receptor. Proc Natl Acad Sci U S A. 1977 Feb;74(2):515-519. DOI: 10.1073/pnas.74.2.515

12. Reid JL. Alpha-adrenergic receptors and blood pressure control. Am J Cardiol. 1986 Mar;57(9):6E-12E. DOI: 10.1016/0002-9149(86)90716-2

13. Ahlquist RP. Present state of alpha- and beta-adrenergic drugs I. The adrenergic receptor. Am Heart J. 1976 Nov;92(5):661-664. DOI: 10.1016/s0002-8703(76)80086-5

14. Van Emmerik-Van Oortmerssen K, Van De Glind G, Van Den Brink W, Smit F, Crunelle CL, Swets M, et al. Prevalence of attention-deficit hyperactivity disorder in substance use disorder patients: a meta-analysis and meta-regression analysis. Drug Alcohol Depend. 2012 Apr;122(1-2):11-9. DOI: 10.1016/j.drugalcdep.2011.12.007

15. Limanaqi F, Gambardella S, Biagioni F, Busceti CL, Fornai F. Epigenetic effects induced by methamphetamine and methamphetamine-dependent oxidative stress. Oxid Med Cell Longev. 2018;2018:4982453. DOI: 10.1155/2018/4982453

16. Sharma G, Sharma N, Nguyen BT, Jeong JH, Nah SY, Yoneda Y, et al. Protective potential of Ginkgo biloba against an ADHD-like condition. Curr Mol Pharmacol. 2021;14(2):200-209. DOI: 10.2174/1874467213666200424152454

17. Huang X, Li N, Pu Y, Zhang T, Wang B. Neuroprotective effects of ginseng phytochemicals: recent perspectives. Molecules. 2019 Aug;24(16):E2939. DOI: 10.3390/molecules24162939

18. Sowndhararajan K, Deepa P, Kim M, Park SJ, Kim S. An overview of neuroprotective and cognitive enhancement properties of lignans from Schisandra chinensis. Biomed Pharmacother. 2018 Jan;97:958-968. DOI: 10.1016/j.biopha.2017.10.145

19. Lee Y, Jung JC, Jang S, Kim J, Ali Z, Khan IA, et al. Anti-Inflammatory and neuroprotective effects of constituents isolated from Rhodiola rosea. Evid Based Complement Alternat Med. 2013;2013:514049. DOI: 10.1155/2013/514049

20. Lyon MR, Cline JC, Totosy De Zepetnek J, Shan JJ, Pang P, Benishin C. Effect of the herbal extract combination Panax quinquefolium and Ginkgo biloba on attention-deficit hyperactivity disorder: a pilot study. J Psychiatry Neurosci. 2001 May;26(3):221-228.

21. Ko HJ, Kim I, Kim JB, Moon Y, Whang MC, Lee KM, et al. Effects of Korean red ginseng extract on behavior in children with symptoms of inattention and hyperactivity/impulsivity: a double-blind randomized placebo-controlled trial. J Child Adolesc Psychopharmacol. 2014 Nov;24(9):501-508. DOI: 10.1089/cap.2014.0013

logo

Your one stop destination for education and clinical tools, driven by our purpose to inspire people to live better lives through natural healthcare.

Customer Care or Clinical Support

1300 654 336

or visit www.myintegria.com

© 2025, Integria is a registered trademark of Integria Healthcare (Australia) Pty Ltd

Terms of Use | Privacy | Policies