Tizanidine: a review of its pharmacology, clinical efficacy and tolerability in the management of spasticity associated with cerebral and spinal disorders

AJ Wagstaff, HM Bryson - Drugs, 1997 - Springer
Synopsis The central α 2 adrenoceptor agonist tizanidine is a myotonolytic agent used in the
treatment of spasticity in patients with cerebral or spinal injury. Wide interpatient variability in …

[HTML][HTML] Central neural organization and control of sympathetic nervous system in mammals

MK Sun - Progress in neurobiology, 1995 - Elsevier
The past decade has witnessed rapid progress in defining neural circuits and mechanisms
in the brain, responsible for regulation of the sympathetic nerve activity and cardiovascular …

Prospective assessment of tizanidine for spasticity due to acquired brain injury

JM Meythaler, S Guin-Renfroe, A Johnson… - Archives of physical …, 2001 - Elsevier
Meythaler JM, Guin-Renfroe S, Johnson A, Brunner RM. Prospective assessment of
tizanidine for spasticity due to acquired brain injury. Arch Phys Med Rehabil 2001; 82: 1155 …

A practical overview of tizanidine use for spasticity secondary to multiple sclerosis, stroke, and spinal cord injury

L Kamen, HR Henney III, JD Runyan - Current medical research …, 2008 - Taylor & Francis
Objective: Tizanidine is an imidazoline central α2-adrenoceptor agonist widely used to
manage spasticity secondary to conditions such as multiple sclerosis (MS), stroke, and …

Inhibitory effects of clonidine and tizanidine on release of substance P from slices of rat spinal cord and antagonism by α-adrenergic receptor antagonists

H Ono, A Mishima, S Ono, H Fukuda, MR Vasko - Neuropharmacology, 1991 - Elsevier
Abstract Effects of clonidine and tizanidine, which have antinociceptive and α 2-agonistic
actions, were studied on the release of substance P from slices of spinal cord from the rat …

A clinical and experimental investigation of the effects of tizanidine in trigeminal neuralgia

GH Fromm, D Aumentado, CF Terrence - Pain, 1993 - Elsevier
Experiments in cats anesthetized with α-chloralose showed that tizanidine (TZD: 5-chloro-4-
(2-imidazolin-2-yl-amino)-2, 1, 3-benzothiodiazole) partly resembled carbamazepine (CBZ) …

Rational and targeted pharmacologic treatment of fibromyalgia

A Barkhuizen - Rheumatic Disease Clinics, 2002 - rheumatic.theclinics.com
Fibromyalgia (FM) is a chronic syndrome characterized mainly by widespread pain,
unrefreshing sleep, disturbed mood, and fatigue. It is a clinical syndrome involving a variety …

Pharmacokinetics of orally administered tizanidine in healthy volunteers

FLS Tse, JM Jaffe, S Bhuta - Fundamental & clinical …, 1987 - Wiley Online Library
The pharmacokinetics of tizanidine, a new centrally acting muscle relaxant, have been
studied in 18 normal male volunteers who received orally a single 5 mg dose, a single 20 …

The neuropharmacology of centrally-acting analgesic medications in fibromyalgia

SG Rao - Rheumatic Disease Clinics, 2002 - rheumatic.theclinics.com
Chronic, widespread pain represents the sine qua non of the fibromyalgia syndrome (FMS),
a fact reflected in the requirements of the American College of Rheumatology's 1990 …

Antinociceptive Interaction of Intrathecal α2-adrenergic Agonists, Tizanidine and Clonidine, with Lidocaine in Rats 

T Kawamata, K Omote, M Kawamata… - The Journal of the …, 1997 - pubs.asahq.org
Background The intrathecal alpha2-adrenergic agonist, clonidine, has been shown to have
considerable antinociceptive effect, although clonidine causes hypotension and …