A new class of drug that could prevent depression and PTSD Rebecca Brachman

So the first antidepressants
were made from, of all things,

rocket fuel, left over after World War II.

Which is fitting, seeing as today,
one in five soldiers develop depression,

or post-traumatic stress disorder or both.

But it’s not just soldiers
that are at high risk for these diseases.

It’s firefighters, ER doctors,
cancer patients, aid workers, refugees –

anyone exposed to trauma
or major life stress.

And yet, despite how commonplace
these disorders are,

our current treatments,
if they work at all,

only suppress symptoms.

In 1798, when Edward Jenner
discovered the first vaccine –

it happened to be for smallpox –

he didn’t just discover
a prophylactic for a disease,

but a whole new way of thinking:

that medicine could prevent disease.

However, for over 200 years,

this prevention was not believed
to extend to psychiatric diseases.

Until 2014, when my colleague and I
accidentally discovered

the first drugs that might prevent
depression and PTSD.

We discovered the drugs in mice,

and we’re currently studying
whether they work in humans.

And these preventative
psychopharmaceuticals

are not antidepressants.

They are a whole new class of drug.

And they work by increasing
stress resilience,

so let’s call them resilience enhancers.

So think back to a stressful time
that you’ve since recovered from.

Maybe a breakup or an exam,
you missed a flight.

Stress resilience
is the active biological process

that allows us
to bounce back after stress.

Similar to if you have a cold
and your immune system fights it off.

And insufficient resilience

in the face of a significant
enough stressor,

can result in a psychiatric disorder,
such as depression.

In fact, most cases
of major depressive disorder

are initially triggered by stress.

And from what we’ve seen so far in mice,

resilience enhancers can protect
against purely biological stressors,

like stress hormones,

and social and psychological stressors,
like bullying and isolation.

So here is an example where we gave mice

three weeks of high levels
of stress hormones.

So, in other words, a biological stressor
without a psychological component.

And this causes depressive behavior.

And if we give three weeks
of antidepressant treatment beforehand,

it has no beneficial effects.

But a single dose of a resilience
enhancer given a week before

completely prevents
the depressive behavior.

Even after three weeks of stress.

This is the first time
a drug has ever been shown

to prevent the negative effects of stress.

Depression and PTSD are chronic,
often lifelong, clinical diseases.

They also increase the risk
of substance abuse, homelessness,

heart disease, Alzheimer’s, suicide.

The global cost of depression alone
is over three trillion dollars per year.

But now, imagine a scenario
where we know someone is predictively

at high risk for exposure
to extreme stress.

Say, a red cross volunteer
going into an earthquake zone.

In addition to the typhoid vaccine,

we could give her a pill or an injection
of a resilience enhancer

before she leaves.

So when she is held at gunpoint
by looters or worse,

she would at least be protected
against developing depression or PTSD

after the fact.

It won’t prevent her
from experiencing the stress,

but it will allow her to recover from it.

And that’s what’s revolutionary here.

By increasing resiliency,

we can dramatically reduce
her susceptibility to depression and PTSD,

possibly saving her from losing her job,
her home, her family or even her life.

After Jenner discovered
the smallpox vaccine,

a lot of other vaccines rapidly followed.

But it was over 150 years

before a tuberculosis vaccine
was widely available.

Why?

In part because society believed

that tuberculosis made people more
sensitive and creative and empathetic.

And that it was caused
by constitution and not biology.

And similar things are still said
today about depression.

And just as Jenner’s discovery
opened the door

for all of the vaccines
that followed after,

the drugs we’ve discovered
open the possibility of a whole new field:

preventative psychopharmacology.

But whether that’s 15 years away,

or 150 years away,

depends not just on the science,

but on what we as a society
choose to do with it.

Thank you.

(Applause)

所以第一批抗抑郁药
是由

二战后遗留下来的火箭燃料制成的。

这是合适的,因为今天,
五分之一的士兵会患上抑郁症,

或创伤后应激障碍或两者兼而有之。

但不仅仅是士兵
面临这些疾病的高风险。

是消防员、急诊室医生、
癌症患者、救援人员、难民——

任何遭受创伤
或重大生活压力的人。

然而,尽管这些疾病很常见,但

我们目前的治疗方法,
如果它们有效的话,

只会抑制症状。

1798 年,当爱德华詹纳
发现第一种疫苗时

——恰好是天花疫苗——

他不仅发现
了一种疾病的预防方法,

而且还发现了一种全新的思维方式:

这种药物可以预防疾病。

然而,200 多年来,

人们认为这种预防措施并未
扩展到精神疾病。

直到 2014 年,我和同事
意外发现

了第一种可能预防
抑郁症和 PTSD 的药物。

我们在老鼠身上发现了这些药物

,我们目前正在研究
它们是否对人类有效。

这些预防性
精神

药物不是抗抑郁药。

它们是一种全新的药物。

它们通过提高
抗压能力发挥作用,

所以我们称它们为抗压增强剂。

所以回想
一下你从那以后恢复的压力时期。

也许分手或考试,
你错过了航班。

压力复原力
是一种积极的生物过程

,它使我们
能够在压力后反弹。

类似于如果您感冒了
并且您的免疫系统可以抵抗它。

面对

足够大的压力源,弹性不足

会导致精神疾病,
例如抑郁症。

事实上,大多数
重度抑郁症

病例最初都是由压力引发的。

从我们目前在老鼠身上看到的情况来看,

复原力增强剂可以
防止纯粹的生物压力源,

如压力荷尔蒙,

以及社会和心理压力源,
如欺凌和孤立。

所以这里有一个例子,我们给老鼠

三周的
高水平压力荷尔蒙。

因此,换句话说,是一种没有心理成分的生物压力源

这会导致抑郁行为。

如果我们事先给予三周
的抗抑郁药治疗,

它没有任何益处。

但是一周前给予的单剂弹性
增强剂

可以完全
防止抑郁行为。

即使经过三周的压力。

这是第
一次有药物被证明

可以防止压力的负面影响。

抑郁症和创伤后应激障碍是慢性的,
通常是终生的临床疾病。

它们还会
增加药物滥用、无家可归、

心脏病、老年痴呆症和自杀的风险。

仅抑郁症的全球成本
每年就超过 3 万亿美元。

但是现在,想象一个场景
,我们知道某人预测

性地面临
极端压力的高风险。

比如说,一名红十字志愿者
进入地震区。

除了伤寒疫苗,

我们可以在她离开之前给她一颗药丸或
注射一种恢复力增强剂

因此,当她
被抢劫者或更糟的枪指着时,

她至少会得到保护,不会在事后
发展成抑郁症或创伤后应激障碍

这不会阻止
她承受压力,

但会让她从中恢复过来。

这就是这里的革命性。

通过提高复原力,

我们可以显着降低
她对抑郁症和 PTSD 的易感性,

可能使她免于失去工作、
家庭、家庭甚至生命。

在詹纳
发现天花疫苗之后

,很多其他疫苗也迅速跟进。

但是,在广泛使用结核病疫苗之前,已经过了 150 多年

为什么?

部分原因是社会

认为结核病使人们更加
敏感、富有创造力和善解人意。

而且它是
由体质而不是生物学引起的。 关于抑郁症,

今天仍然有人说类似的话

正如詹纳的发现

为随后的所有疫苗打开了大门一样,

我们发现的药物也
开启了一个全新领域的可能性:

预防性精神药理学。

但是,这是 15 年后

还是 150 年后,

不仅取决于科学,

还取决于我们作为一个社会
选择用它做什么。

谢谢你。

(掌声)