Larry Byrd:
A lifetime of addicting monkeys and apes to
illegal drugs
In 1997, anti-cruelty activists
encamped at the entrance to Emory University, home to Yerkes Regional
Primate Research Center, were accosted by a few students who were
certain that what was being alleged as occurring in the Yerkes labs
was incorrect. They based their criticisms on what they felt was
incontrovertible fact: Larry Byrd, a vivisector named in some of
the materials being handed out, had retired. This, they claimed,
proved that the activists had their facts wrong. They said that,
yes, Byrd had performed questionable experiments, but that he was
now gone, and that such experiments would not be allowed today.
Apparently, Emory is graduating students ignorant of what has occurred
and is occurring on their campus. While Byrd did indeed retire from
teaching, his sick experiments on monkeys did not.
Larry Byrd has spent an entire lifetime giving street drugs to monkeys
and other animals. Decades of research used squirrel monkeys. Just
prior to retiring he was addicting pregnant rhesus macaque mothers.
He wrote, "During the past year, cocaine-exposed juveniles
and their pair-fed controls were tested on several measures of cognition
and memory, and sensitivity to pharmacological disruption of behavioral
performances was determined." That study earned him $399,556.
Larry D. Byrd, Chief of Behavioral Biology at Yerkes.
1981, Research Professor, Yerkes Primate Research Center;
Professor of Pharmacology. B.A., East Carolina University, 1962;
M.A., 1964;
Ph.D., University of North Carolina/Chapel Hill, 1968.
For nearly a quarter of a century Larry Byrd has consumed public
funds. The millions of dollars he has squandered have done nothing
to improve human health. He has used our money to force chimpanzees,
baboons, macaque monkeys, squirrel monkeys and rats to inject themselves
with cocaine and speed (d-amphetamine) and has punished them with
electric shocks when they have resisted.
When Larry Byrd’s addiction experiments became boring, he
also dabbled in the effects of coffee, ways to cause paralysis,
and techniques for turning his victims into living chemical laboratories.
And of course, he jumped onto the AIDS gravy-train for a while as
well.
Below is a history of Larry Byrd’s life’s-work told
through the papers he has published:
2001: Fetal development in rhesus monkeys exposed prenatally
to cocaine.
Howell LL, Schama KF, Ellis JE, Grimley PJ, Kitchens AJ, Byrd LD.
Neurotoxicol Teratol. 2001 Mar-Apr;23(2):133-40.
2001: Effects of morphine on T-cell recirculation in rhesus
monkeys.
Donahoe RM, Byrd LD, McClure HM, Brantley M, Wenzel D, Ansari AA,
Marsteller F. Adv Exp Med Biol. 493:89-101.
2000: Behavioral evaluation of hemiparkinsonian MPTP monkeys
following dopamine pharmacological manipulation and adrenal co-graft
transplantation.
Howel LL, Byrd LD, McDonough AM, Iuvone PM, Bakay RA.
Cell Transplant. Sep-Oct;9(5):609-22.
1997: Serotonergic modulation of the discriminative-stimulus
effects of cocaine in squirrel monkeys.
Schama K, Howell LL, Byrd LD
Psychopharmacology (Berl) Jul 132:1 27-34
1995: Serotonergic modulation of the behavioral effects of
cocaine in the squirrel monkey.
Howell LL, Byrd LD
J Pharmacol Exp Ther. Dec 275:3 1551-9
1993: Consequences of opiate-dependency in a monkey model
of AIDS.
Donahoe RM, Byrd LD, McClure HM, Fultz P, Brantley M, Marsteller
F, Ansari AA, Wenzel D, Aceto M
Adv Exp Med Biol. 335: 21-8
1993: Effects of CGS 15943, a nonxanthine adenosine antagonist,
on behavior in the squirrel monkey.
Howell LL, Byrd LD
J Pharmacol Exp Ther. Oct 267:1 432-9
Abstract:
"The similarity of the effects of CGS 15943 and caffeine supports
and extends previous findings suggesting that the behavioral-stimulant
effects of caffeine and other xanthines are mediated through adenosine-antagonist
actions rather than inhibition of PDE activity."
1993: In utero exposure to cocaine: a review.
Ellis JE, Byrd LD, Sexson WR, Patterson-Barnett CA
South Med J. 1993 Jul 86:7 725-31
Abstract
"Substantial data have been derived from clinical observations,
clinical studies, and animal studies indicating that prenatal exposure
to cocaine may have detrimental short-term and possibly long-term
effects on the mother, the developing fetus, and the neonate. …Prospective
controlled studies are needed to define further the effects of cocaine
as distinct from other negative influences having an impact on the
developing fetus, the newborn, or the infant." [2001: Maternal
food consumption and body weight increased during pregnancy, and
there were no significant differences among experimental groups.
Although both groups with a history of cocaine exposure had lower
survival rates compared to pair-fed controls, of the fetuses that
survived, fetal heart rate, fetal biparietal diameter, and mean
gestational length were in the normal range for all experimental
groups. Similarly, body weight, biparietal diameter, body length,
and modified Apgar scores at birth did not differ significantly
among experimental groups. The results indicate that surviving fetuses
exhibited normal growth. (From: Fetal development in rhesus monkeys
exposed prenatally to cocaine, above.)]
1992: A method for quantitating motor deficits in a nonhuman
primate following MPTP-induced hemiparkinsonism and co-grafting.
Ellis JE, Byrd LD, Bakay RA
Exp Neurol. Mar 115:3 376-87
Abstract:
"This report describes a nonhuman primate model of MPTP-induced
hemiparkinsonism and the recovery of motor function following co-grafting
of adrenal medullary tissue and peripheral nerve into the lesioned
area of the brain. A rhesus monkey (Macaca mulatta) trained to perform
a complex, discrete-trial, operant task served as the subject. After
behavioral performance on the task had stabilized and a high level
of accuracy was maintained, 0.4 mg/kg MPTP was infused acutely via
the left carotid artery to produce a marked impairment of movement
of the right arm."
In English: A rhesus monkey was trained to perform a circus trick
that required the use of one arm. Though the abstract does not give
details, it is likely that the monkey was trained to pull a lever
when a light flashed - or something similar. The monkey was likely
trained using a reward/punishment method. The monkey probably received
a raisin (or something similar) when he or she performed well, and
an electric shock when performance was poor.
Once the monkey knew the trick, a poison was injected into an artery
in the monkey's neck, which killed part of his or her brain. Larry
Byrd could tell that part of the monkey’s brain had died
because the monkey could not perform the trick as well as before
it was poisoned. He later operated on the monkey’s brain
and was able to fix it up a little bit. Of course, the monkey was
never totally cured and was eventually killed so the monkey's brain
could be sliced up and examined.
1992: Enhanced sensitivity to the behavioral effects of cocaine
after chronic administration of D2 -selective dopamine antagonists
in the squirrel monkey.
Howell LL, Byrd LD
J Pharmacol Exp Ther. Sep 262:3 907-15
1991: Characterization of the effects of cocaine and GBR
12909, a dopamine uptake inhibitor, on behavior in the squirrel
monkey.
Howell LL, Byrd LD
J Pharmacol Exp Ther. Jul 1 258:1 178-85
1990: Effects of dominance rank on d-amphetamine-induced
increases in aggression.
Martin SP, Smith EO, Byrd LD
Pharmacol Biochem Behav. Nov 37:3 493-6
Abstract
"These data support the hypothesis that the dominance position
of an animal in a group can be a determinant of the behavioral effect
of certain drugs."
1988: Differential effects of cocaine and pentobarbital on
fixed-interval and random-interval performance.
Howell LL, Byrd LD, Marr MJ
J Exp Anal Behav. May 49:3 411-28
Abstract
"To investigate the purported relationship between control
rate and drug rate, squirrel monkeys were trained under a fixed-interval
300-s schedule of stimulus-shock termination, a procedure that engendered
a wide range of response rates. A light illuminated the experimental
chamber during the fixed interval, and the first lever press after
300 s had elapsed terminated the light for 30 s and precluded an
electrical stimulus to the tail."
1987: Extracellular dopamine in rat striatum following uptake
inhibition by cocaine, nomifensine and benztropine.
Church WH, Justice JB Jr, Byrd LD
Eur J Pharmacol. Jul 23 139:3 345-8
1986: Similarities in the rate-altering effects of white
noise and cocaine.
Howell LL, Byrd LD, Marr MJ
J Exp Anal Behav. Nov 46:3 381-94
1986: Effects of d-amphetamine on grooming and proximity
in stumptail macaques: differential effects on social bonds.
Peffer PG, Byrd LD, Smith EO
Pharmacol Biochem Behav. Apr 24:4 1025-30
Abstract
"The acute administration of d-amphetamine (0.01-0.3 mg/kg
IM) resulted in marked increases in the rate of self-grooming, i.e.,
the number of self-grooming bouts initiated per hour, for all subjects
and in decreases in the rate at which subjects groomed other monkeys,
but the drug appeared to have no effect on the rate at which a subject
positioned itself near another monkey."
1985: d-Amphetamine induced changes in social interaction
patterns.
Smith EO , Byrd LD
Pharmacol Biochem Behav. Jan 22:1 135-9
Abstract
"The behavioral effects of d-amphetamine were studied in a
group of stumptail macaques in a large outdoor enclosure. d-Amphetamine
altered characteristic patterns of aggressive and affiliative behaviors
in adult males that received the drug. Each monkey that received
d-amphetamine increased its aggression toward non-adult animals
in the group and decreased aggression toward adult members."
1983: Cardiovascular effects of naloxone, naltrexone and
morphine in the squirrel monkey.
Byrd LD
Life Sci. Jan 24 32:4 391-8
Abstract
"Heart rate (HR) and mean arterial blood pressure (BP) were
recorded from conscious, chair-restrained squirrel monkeys surgically
prepared with chronically indwelling arterial and venous catheters
. . ."
1983: Studying the behavioral effects of drugs in group-living
nonhuman primates.
Smith EO , Byrd LD
Prog Clin Biol Res. 131: 1-31
1982: Comparison of the behavioral effects of phencyclidine,
ketamine, d-amphetamine and morphine in the squirrel monkey.
Byrd LD
J Pharmacol Exp Ther. Jan 220:1 139-44
1981: Time-course effects of adrenergic and cholinergic antagonists
on systemic arterial blood pressure, heart rate and temperature
in conscious squirrel monkeys.
Byrd LD, Gonzalez FA
J Med Primatol. 10:2-3 81-92
Abstract
"Mean arterial blood pressure, heart rate, and rectal temperature
were measured from conscious, chair-restrained squirrel monkeys
prepared with chronically indwelling arterial and venous catheters
and temperature probes to determine the magnitude and duration of
the effects of acute intravenous injections of propranolol, phentolamine
and methyl atropine."
1980: Time-course effects of two barbiturates on cardiovascular
activity and temperature in the squirrel monkey.
Byrd LD
Life Sci. Sep 15 27:11 935-42
1980: Magnitude and duration of the effects of cocaine on
conditioned and adjunctive behaviors in the chimpanzee.
Byrd LD
J Exp Anal Behav. Jan 33:1 131-40
Abstract
"Conditioned and adjunctive behaviors were disrupted and suppressed
for different durations at 10.0 mg/kg, a dose which induced convulsive
seizures within 10 minutes after intramuscular injection."
1979: A tethering system for direct measurement of cardiovascular
function in the caged baboon.
Byrd LD
Am J Physiol. May 236:5 H775 -9
1977: Physiological effects of cocaine in the squirrel monkey.
Gonzalez FA, Byrd LD
Life Sci. Nov 15 21:10 1417-24
Abstract
"A device suitable for the continuous measurement of physiological
activity in large, conscious monkeys has permitted the direct recording
of systemic arterial blood pressure and heart rate in caged baboons.
The device comprises a lightweight fiberglass backpack, retained
in place on the baboon by a thoracic elastic band and shoulder straps,
and a flexible stainless steel tether connecting the pack to an
electrocannular slip-ring in the top center of the baboon's cage.
A chronically indwelling arterial catheter inserted retrograde into
the abdominal aorta via the internal iliac artery and connected
to a small pressure transducer on the pack provides direct measurement
of blood pressure and heart rate. Body fluids can be sampled or
drugs administered via an indwelling catheter in the inferior vena
cava. Electrical and fluid connections between the fiberglass pack
and recording and infusion equipment located outside the cage pass
through the flexible tether and remain protected from the subject.
The reliability of the tethering system has been demonstrated in
physiological, pharmacological, and behavioral experiments with
baboons."
1976: Effects of morphine alone and in combination with naloxone
or d-amphetamine on shock-maintained behavior in the squirrel monkey.
Byrd LD
Psychopharmacology (Berl) Sep 29 49:3 225-34
Abstract
"Key-pressing behavior in the squirrel monkey was maintained
under an 8-min fixed-interval (FI) schedule of electric-shock delivery."
1975: Contrasting effects of morphine on schedule-controlled
behavior in the chimpanzee and baboon.
Byrd LD
J Pharmacol Exp Ther. Jun 193:3 861-9
Abstract
"A similar depression of respiration was not observed in the
increase responding in a nonhuman primate, the chimpanzee, and that
the behavioral effects of morphine in the chimpanzee are qualitatively
different from the effects in monkeys."
1974: Modification of the effects of chlorpromazine [Thorazine]
on behavior in the chimpanzee.
Byrd LD
J Pharmacol Exp Ther. Apr 189:1 24-32
1973: Effects of d-amphetamine on schedule-controlled key
pressing and drinking in the chimpanzee.
Byrd LD
J Pharmacol Exp Ther. Jun 185:3 633-41
Larry Byrd: a lifetime spent abusing animals.
Emory University owes everyone an explanation.
Rick Bogle, 1997 (revised, 2002)
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