BMJ 1998;317:1136-1138 ( 24 October )
Clinical review
Fortnightly review
Magic bullet for obesity
Jules Hirsch, Sherman
Fairchild professor.
Rockefeller University, New
York, NY 10021-6399 USA
Hirsch{at}raockvax.rockefeller.edu
Who would not rejoice to find a magic bullet that we could
fire into obese people to make them permanently slim and healthy? In
the United States about a third of adults are obese
that is, have a
body mass index (weight(kg)/height(m)2)) above
27.1 The diagnosis can be made with reasonable accuracy by
anyone. Obese people appear "chunky" and usually have some abdominal protuberance with or without unsightly thighs. Tens of
billions of dollars are spent on diets, pills, spas, or special foods
and advice on behavioural change. Any scientific discovery that deals
with food intake or obesity quickly becomes a "hot item" for the
media. The best seller list usually contains a book giving
recommendations for a new diet or mixture of diet and behaviour that
assures successful weight control. Medical authorities, particularly public health officials, warn the public of the rising prevalence and
hazards of obesity.
A recent editorial in the New England Journal of Medicine
documented the failures of current treatment and questioned the benefits of weight loss while reminding us of the strong correlation of
obesity with disorders such as hypertension and diabetes.2 Since current treatment so often fails, only a magic bullet would allow
us to perform an experiment to determine the full benefit of weight
loss. Are we on the brink of finding a drug which will solve the
problem?
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Summary points
More and more people in developed countries are becoming obese,
and millions of pounds are spent on overcoming it
Drug treatments have so far had limited efficacy and some have had
serious side effects
Maintenance of energy balance is complex and affected by hormonal,
genetic, psychosocial, and environmental factors
Genetic studies seem unlikely to reveal a universal magic bullet in the
near future, although treatments for people with rare mutations may be
identified
The search for a magic bullet remains worth while as it increases our
understanding of the control of energy metabolism
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Methods |
This article is based on my observations and a review of recent
literature on drug treatment of obesity.
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Drugs for obesity |
For many years sympathetic agonists such as amphetamines, which
have a transient anorexigenic effect, were used to treat obesity. Although over the counter preparations such as phenylpropanolamine with
or without caffeine were still being purchased, by 1992 drug treatment
for obesity was losing its appeal. The main approaches to reducing
obesity were low fat diets and increased physical activity with or
without behavioural modification.
A new wave of enthusiasm for pharmacological treatment developed after
the publication of a study showing that a combination of phentermine,
an amphetamine-like drug, and fenfluramine, a serotonin reuptake
inhibitor, led to weight reduction that persisted for long
periods.3 This raised enormous excitement, even though careful review of the published results revealed that only about a
fifth of those who began the study completed the full three to four
year treatment and that those who stayed the course lost only about 9%
of initial body weight. Furthermore, the effect seemed to be waning in
some who continued the treatment.4
The fusillade of not so magic bullets reached its peak in 1996, when 18 million prescriptions for phentermine and fenfluramine were written and
more than 2 million for the newest addition, dexfenfluramine.5 Dexfenfluramine is one of two isomers of fenfluramine and has the full anorexigenic action but fewer side effects than the mixture of isomers. The long term effects of the new
drugs were not fully evaluated, but a good guess is that patients could
achieve a 10 to 12% reduction in body weight in one year, although
this would not be fully maintained with continued treatment
hardly a
magic bullet. It turned out, however, that the so called "phen-fen"
combination might be more bullet than magic. Many people who received
the drugs developed unexpected cardiac valvular disturbances, and
dexfenfluramine was removed from the UK and American markets last year.
Present candidates for the magic bullet include sibutramine, a drug
which inhibits reuptake of both serotonin and noradrenaline to induce
anorexia; olestra, a fat substitute which has the qualities of fat but
cannot be absorbed; and orlistat, which blocks the action of pancreatic
lipase thereby inhibiting fat absorption. To assess the likelihood of
success of these new agents it is useful to step back and review our
understanding of the regulation of energy metabolism in humans and its
most prevalent disturbance, obesity.
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Maintaining energy balance |
In a recent review my colleagues and I emphasised the incredible
intricacy and complexity of the system that maintains a fixed level of
energy storage.6 The balance of food intake and energy expenditure that maintains constant energy storage either at normal or
obese levels is determined by the metabolism of muscle, liver, pancreas, and intestine. The balance is regulated by the adrenal and
sex steroids as well as adipose tissue itself, which together create a
complex set of signals that are centrally transduced into autonomic
nervous and humoral controls affecting energy dissipation and food
intake. Hovering over this complex system are potent psychosocial and
behavioural factors. The total system assures relatively constant fat
storage in adipose tissue and responsiveness to external environmental
events such as the scarcity of food or cultural aspects of food intake
and physical activity.

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Living in hope of a magic bullet?
CREDIT: HORENSTEIN/PHOTONICA
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There are so many redundant pathways and accessory means of controlling
energy metabolism that any single alteration is unlikely to change the
level of fat storage in the long run. For a drug to be even partially
helpful it must traverse and impair the function of several important
loops in the system, which makes it likely that unwanted adverse
effects will occur. Treatment will have to be aimed at a large
proportion of the population, daily and for life. With pervasive
slimness-seeking in our culture, the potential for abuse or misuse of
such drugs is of great concern. Without full knowledge of how the
system works more harm may be caused than help. Bullets shot into
control mechanisms will produce weight loss for a while, but no magic
bullet yet exists that can strike the central control mechanism and
make permanent changes in fat storage with either no adverse effects or
so few side effects that the biological price would be acceptable.
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Genetic factors |
Filling in all the gaps of the organisational plan for the control
of energy metabolism is the next step in the search for a magic bullet.
If we can localise the central control mechanisms or particularly
powerful elements that set the level of fat storage then perhaps we
could devise magic bullets to reset these mechanisms and thereby
eradicate obesity. Genetic studies are now adding new information to
the organisational map. Knowledge based on physiological and
biochemical observations along with the effects of specific brain
ablation and brain stimulation is being enriched by study of the genome
in rodent mutants that become obese. Five mutant mouse obesities and
one rat obesity have been known for years, but the exact location of
the genetic defects in these animals has been ascertained only
recently.7 All mutant genes responsible for animal
obesities have now been identified, and strong homology exists between
the rodent genes and human genes. Furthermore, the evidence for genetic
factors in human obesity has become increasingly strong with studies of
twins and families with and without obesity.
An example of the relation of these genes to human obesity is given by
the ob mouse. The mouse carries a recessive autosomal disorder
resulting in the inability of adipose tissue to secrete the protein
leptin. Leptin functions as a signal to the central nervous system for
both food intake and energy expenditure, and in the homozygous ob mouse
leptin deficiency resets the control mechanisms to the obese state. For
such animals, leptin is indeed a magic bullet. Although humans produce
leptin, deficiency is extraordinarily rare.8 But the ob
and other mouse mutants do give new information about the organisation
of energy control.
Other mutations such as those that produce the rodent obesities have
been sought in humans but must be very rare. They are rare in rodents
as well. Nevertheless, the pharmaceutical and biotechnology industries
are investigating the rodent mutant genes and the peptides with which
they interact, such as neuropeptide Y, to determine their potential for
treatment of obesity. The products of these genes seem likely to become
magic bullets only in those instances in which there is a homologous
human gene mutation. Since this is rarely the case, it is hard to be
optimistic that the right bullet is on the horizon.
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Will there ever be a magic bullet? |
The astonishing increase in obesity when food is plentiful and we
are enticed into greater consumption of food and reduced energy
expenditure suggest that the genetic factors which control energy
metabolism are responsive to environmental influences during growth and
development. The relatively long infancy and childhood of humans
compared with other animals suggests that early environmental effects
may exist. If human obesity is a multigenic event and growth and
development can be altered by differential environmental effects on
many genes, the system is much more intricate than that found in
rodents. But the search for bullets, even before the mechanism that
controls energy metabolism is fully understood, remains valuable. Each
step forward gives better definition of the control systems, and
ultimately this information can be used along with careful observation
and experimental analysis of the genetic events that are active and
modifiable at each stage of growth and development. It may be that only
in the rarest instances can the final structural "set" be reversed
by any bullet, but means may be found to reverse the interaction
between obesity and the most important associated illness
type II
diabetes. Even better, would be safe interventions at early stages of
development to prevent the occurrence of obesity in the first place.
Thus, the possibility of finding a magic bullet for obesity may be
remote, but the search is important because it uncovers new information
about how we develop and how we manage the mysterious energy balance
over so much of our lives. There may never be a magic bullet, but the
search is a new and important target for the drug industry and could
lead to some pharmacological help in curbing the current epidemic of
obesity.
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© BMJ 1998